ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • General Chemistry  (4,294)
  • Inorganic Chemistry  (3,763)
  • Man/System Technology and Life Support  (2,328)
  • Fisheries
  • 2010-2014  (2,375)
  • 1975-1979  (8,086)
Collection
Keywords
Publisher
Years
Year
  • 1
    facet.materialart.
    Unknown
    Ctenochaetus marginatus (Valenciennes) (Pisces: Acanthuridae) en la Isla de Gorgona: Primer registro del género para el Pacífico colombiano (2010)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: The genus Ctenochaetus is reportad in the waters of the Colombian Pacific based on two specimens of C. marginatus (Valenciennes) collected in 1993 at Gorgona Island (2°59' N, 78° 12' W). These specimens differ inseveral morphometric characteristics from thosepreviously examined. Such differences appear to be an artifact of the small number of specimens formerly examined and the consequent narrow ranges reportad. We suggest that temperature variability affects the distribution of C. marginatus in the tropical eastern Pacific.
    Description: El género es Ctenochaetus reportad en las aguas del Pacífico colombiano a partir de dos especímenes de C. marginatus (Valenciennes) recogidos en 1993 en la Isla Gorgona (2 ° 59 'N, 78 ° 12' W). Estos ejemplares difieren inseveral características morfométricas de thosepreviously examinados. Estas diferencias parecen ser un artefacto del pequeño número de muestras examinadas anteriormente y reportad los rangos estrechos consecuente. Sugerimos que la variabilidad de la temperatura afecta la distribución de marginatus C en el Pacífico tropical oriental.
    Description: Published
    Keywords: Fisheries ; Fisheries
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 2
    facet.materialart.
    Unknown
    Going against the flow: Effects of river damming in Cuban fisheries (2013)
    Details
    Publication Date: 2021-05-19
    Description: Over the last decade eutrophication of freshwater artificial reservoirs in Cuba occurred in parallel to oligotrophication of estuarine and coastal waters. These two processes influenced both freshwater and marine fisheries. A dramatic shift in species composition in freshwater fisheries has occurred, from dominance by cichlids (tilapia) to dominance by cyprinids. The high fishery yield from some reservoirs, and shift in species composition, seems related to progressive eutrophication of reservoirs by nutrient subsidies from different anthropogenic activities; particular those related to the size of urban areas within their watersheds. On the other hand, marine landings of estuarine-dependent species declined more significantly than for other groups associated with seagrass beds–coral reefs and oceanic waters. The ratio between catches of estuarine-dependent species and those associated with seagrass beds and coral reefs, decreased significantly over the last 20 years. The decrease in landings was more evident in typical estuarine species, such as shrimps (Litopenaeus schmitti and Farfantopenaeus notialis), mangrove oyster (Crassostrea rhizophorae) and mullets (Mugil spp.). River damming increased during the same period and is significantly correlated with these decreases. It is hypothesized that two different processes acted synergistically, leading to dramatic decreases of several orders of magnitude, in the catches of estuarine species over the last decade: the trapping of nutrients and sediments by river damming, and a drastic reduction in nutrient inputs from land-based sources due to reduced fertilizer use. These are postulated to have affected not only estuarine resources, but also the whole coastal ecosystem.
    Description: Durante la última década, la eutrofización de los embalses artificiales de agua dulce en Cuba se produjo en paralelo a oligotrophication de estuarios y costeras aguas. Estos dos procesos de influencia de agua dulce y la pesca marina. Un cambio dramático en la composición de las especies en la pesca de agua dulce se ha producido, de la dominación de los cíclidos (tilapia) a la dominación de ciprínidos. La alta producción de la pesca de algunos embalses, y el cambio en las especies composición, parece relacionada con la progresiva eutrofización de los embalses de las subvenciones de nutrientes de diferentes actividades antropogénicas, especialmente las relacionado con el tamaño de las zonas urbanas dentro de sus cuencas. Por otro lado, los desembarques de especies marinas de estuario-dependientes disminuyeron significativamente más que para otros grupos asociados con algas marinas Los arrecifes de coral-camas y las aguas oceánicas. La relación entre las capturas de las especies que dependen de los estuarios y las asociadas a las praderas marinas y Los arrecifes de coral, se redujo significativamente en los últimos 20 años. La disminución en los desembarques fue más evidente en especies típicas de estuarios, tales como camarones (Litopenaeus schmitti y Farfantopenaeus notialis), ostra de mangle (Crassostrea rhizophorae) y la lisa (Mugil spp.). El represamiento del Río aumentó durante el mismo período y se correlaciona significativamente con estas disminuciones. Se planteó la hipótesis de que dos procesos diferentes actúan de forma sinérgica, que conduce a una disminución drástica de varios órdenes de magnitud, en las capturas de las especies de estuario en la última década: la captura de nutrientes y sedimentos por represas río, y una reducción drástica de los aportes de nutrientes de fuentes terrestres, debido a la reducción del uso de fertilizantes. Se postula que han afectado no sólo a los recursos estuarinos, sino también todo el ecosistema costero.
    Description: Published
    Description: ríos
    Description: impactos antropogénicos
    Keywords: river ; Fisheries ; Eutrophication
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 3
    facet.materialart.
    Unknown
    Capturas de sierras, serruchos y pintadas con redes de enmalles (2013)
    Details
    Publication Date: 2021-05-19
    Description: Se muestra la evolución de las capturas de las sierras y pintadas, se describen las 3 maneras en que las especies pueden quedar atrapadas en la redes de enmalles, así como también los tipos de redes (deriva, media agua y de fondo).
    Description: Published
    Description: Scomberomorus regalis
    Description: Scomberomorus maculatus
    Description: Scomberomorus cavalla
    Description: spanish mackerel
    Description: king mackerel
    Description: painted mackerel
    Description: enmalle
    Description: arte de pesca
    Keywords: Fisheries ; Artisanal fishing
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 4
    facet.materialart.
    Unknown
    Las pesquerías de lisas y mojarras en lagunas costeras. (2013)
    Details
    Publication Date: 2021-05-19
    Description: Published
    Description: Mugil curema
    Description: Mugil liza
    Description: Mugil cephalus
    Description: Gerres cinereus
    Description: patao
    Description: coastal lagoons
    Keywords: Mullet fisheries ; Fisheries
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 5
    facet.materialart.
    Unknown
    Tensores naturales y antrópicos al norte de Villa Clara, Cuba; efectos en la producción de ostión (crassostrea rhizophorae, Guilding, 1828) (2010)
    Details
    Publication Date: 2021-05-19
    Description: Production of mangrove oyster (Crassostrea rhizophorae Guilding, 1828), north of Villa Clara, Cuba Province, tends to decline since 1980, accentuating from 2003 on. Despite regulations to protect the resource, minimum legal size and catch closures, the year 2008 presents the landing smaller volumes of the past 50 years. An analysis of the variability of catches in relation to natural and human factors, allows for precipitating causes of low productivity of this fishery resource; between the most representatives are expanding storage capacity of river water, salinity increment, the increase in frequency and intensity of hurricanes and the mismanagement of the extraction of oyster.
    Description: La producción de ostión de mangle (Crassostrea rhizophorae, Guilding, 1828), al norte de la provincia de Villa Clara, Cuba, tiende a la disminución desde de 1980, acentuándose a partir del año 2003. A pesar de regulaciones para la protección del recurso, talla mínima legal y vedas de captura, el año 2008 presenta los menores volúmenes de desembarque de los últimos 50 años. Un análisis de la variabilidad de las capturas, en relación con factores naturales y antrópicos, permite establecer causas desencadenantes de la baja productividad de este recurso pesquero; las más representativas son, la ampliación en la capacidad de embalse de aguas fluviales, aumentos de la salinidad, el incremento en la frecuencia e intensidad de los huracanes y un manejo inadecuado de la actividad extractiva de ostión.
    Description: Crassostrea rhizophorae, Cuba
    Keywords: Fisheries ; Environmental effects ; Fisheries
    Repository Name: AquaDocs
    Type: Preprint
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 6
    facet.materialart.
    Unknown
    Caso de Estudio No. 2: Estado de la pesquería de la langosta espinosa (Panulirus argus) y su relación con factores ambientales y antrópicos en Cuba. (2011)
    Instituto de Oceanología | Cuba
    Details
    Publication Date: 2021-05-19
    Description: Las capturas de langosta espinosa Panulirus argus (Latreille, 1804) en Cuba alcanzaron sus mayores volúmenes en la década de 1980 con un promedio anual de 11565 ton. En la década de 1990, la captura descendió a un promedio de 9327 ton, lo cual se ha visto agudizado entre 2000 y 2007 con un promedio de 6262 ton y una mayor variabilidad de las capturas, a pesar de un perfeccionamiento del sistema de manejo pesquero dado por: la disminución del esfuerzo pesquero y de la tasa de mortalidad por pesca desde 1999, el aumento del período de veda desde 2001 y el incremento gradual de la talla mínima legal de captura a partir de 2004. Los análisis más recientes sobre el estado de esta pesquería fueron presentados en el Quinto Taller Regional sobre la Evaluación y la Ordenación de la Langosta Común del Caribe en septiembre 2006 (Puga et al, 2006; FAO, 2007), donde se reconoció por la comunidad científica especializada que la pesquería de langosta cubana se encontraba bien manejada y plenamente explotada (no sobre- explotada) y se concluyó que además de la mortalidad por pesca, otros factores ajenos al sector pesquero estaban produciendo afectaciones en la abundancia del recurso, al causar daños al hábitat 1 en zonas de cría, influyendo negativamente por esta vía sobre el reclutamiento y la producción de langostas. Entre estos aspectos para Cuba se señalaron: la mayor frecuencia e intensidad de huracanes durante el último decenio, el desarrollo de las zonas costeras, la construcción de presas en las cuencas de captación de los ríos y de carreteras en el Archipiélago Sabana-Camagüey comunicando la isla principal con los cayos y los cayos entre si (pedraplenes).
    Description: Published
    Keywords: Fisheries ; Lobster fisheries ; Fisheries ; Environment management ; Recruitment ; Coastal zone management
    Repository Name: AquaDocs
    Type: Book Section
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 7
    facet.materialart.
    Unknown
    Fauna asociada a la pesca del mero Epinephelus Morio (serranidae: pisces) con palangre de fondo en el Banco de Campeche, México. (2010)
    Details
    Publication Date: 2021-05-19
    Description: Se efectúa un estudio de la fauna acompañante del Mero, Epinephelus morio, en la pesquería con palangre de fondo del Banco de Campeche, México, durante el periodo 1987-2009. En la investigación se consideró información de 32 cruceros de investigación realizados en la etapa como parte del convenio pesquero firmado por Cuba y México para la evaluación sistemática del recurso. Se determinó la composición por especie y talla de las capturas, sus variaciones en la abundancia relativa, estructura de tallas, así como el índice de diversidad de Brillouin, la riqueza de especies (Margalef, 1980), la dominancia numérica y la constancia, estas ultimas valoradas según el esquema propuesto por Bodenheimer (1955). Se encontró que la fauna acompáñate de E. morio esta representada por 69 especies, agrupadas en 3 clases y 12 órdenes. De ellos, el orden mejor representado lo constituyó Perciformes con las familias Serranidae, Lutjanidae, Scombridae, Carangidae y Haemulidae como las más abundantes en número. Dentro de estas, dominaron las especies L. campechanus y O. chrysurus, apreciándose que las entidades mejor representadas son, L. campechanus (100%), O. chrysurus (96,87%) y M. bonaci (73,2%). Los largos medios observados se encontraron por encima de las tallas de primera maduración reportadas en la literatura. Sólo E. nigritus y L. analis presentaron individuos inmaduros. Se reportan tallas máximas superiores a las reportadas en la bibliografía en M. interstitiaslis (150cm), M. bonací (155cm) y E. nigritus (125cm). Se determinó que el rendimiento (cpue) y la diversidad de la fauna acompañante poseen una relación inversa con la disminución de la biomasa de mero. Por su parte, la diversidad y riqueza de especie presentaron sus mayores valores concordando con las temporadas de lluvias.
    Description: Mero Epinephelus morio, fauna acompañante, Banco de Campeche, México,
    Keywords: Fisheries ; Fauna ; Fisheries ; Fauna
    Repository Name: AquaDocs
    Type: Preprint
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 8
    facet.materialart.
    Unknown
    Monitoreo anual de la pesquería del cobo (eustrombus gigas) en Caibarién, cayería norte de Villa Clara en el 2011. (2012)
    Details
    Publication Date: 2021-05-19
    Description: Se presentan los resultados de monitoreo de las poblaciones comerciales de cobo en el área comprendida entre los cayos El Cabezo y Boca de Sagua (220 49`N--230 04`N y los 790 35W—800 07´ `W), plataforma Norte de la Provincia de Villa Clara. A partir de los resultados de las densidades de individuos como índice de la abundancia y la estructura poblacional encontrada, se propone un potencial de captura de 104 TM (peso entero). Además, se definen las medidas de manejo para el uso sostenible del recurso Eustrombus gigas en esta zona. El aprovechamiento en carne desembarcada (Eviscerada y sin manto) para individuos adultos con talla comercial se obtiene por un factor de 0,074 (7,4%) del peso entero, que representa 7,7 TM. Se excluye el área protegida desde Las Picúas hasta Cayo Cristo.
    Description: cobo (Eustrombus gigas), Caibarién, Villa Clara
    Keywords: Monitoring ; Fisheries management ; Fisheries
    Repository Name: AquaDocs
    Type: Preprint
    Format: 4
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 9
    facet.materialart.
    Unknown
    Etude environnementale et sociale du PRAO (Cap Vert, Sierra Léone, Libéria, Sénégal) (2010)
    Details
    Publication Date: 2021-05-19
    Description: La Commission Sous Régionale des Pêches (CSRP), qui est un organisme intergouvernemental de coopération halieutique dont l’objectif global est l’harmonisation à long terme, des politiques des pays membres en matière de préservation, de conservation et d'exploitation durable de leurs ressources halieutiques et le renforcement de leur coopération au profit du bien-être de leurs populations respectives, a obtenu par l’intermédiaire de la Banque mondiale, un Don du Fonds pour l’Environnement Mondial (FEM) et du Gouvernement du Japon, pour la préparation d’un Projet Régional des Pêches en Afrique de l’Ouest (PRAO) pour trouver une solution à la problématique susvisée. Ce projet implique 9 pays côtiers: la Mauritanie, le Cap Vert, le Sénégal, la Gambie, la Guinée Bissau, la Guinée, le Sierra Léone (Etats membres de la CSRP), ainsi que le Libéria et le Ghana. Le PRAO comprend trois composantes : (1) Bonne Gouvernance et Gestion Durable des Pêches ; (2) Réduction de la Pêche Illicite ; (3) Augmentation de la Contribution des Ressources Halieutiques dans les Economies Locales (incluant la réalisation d’infrastructures et équipements dans les pêcheries). Certes, les activités prévues dans le cadre du PRAO sont pressenties pour contribuer au développement du secteur de la pêche dans les pays ciblés et apporter des bénéfices aux populations locales. Toutefois, elles pourraient engendrer dans certains cas des effets négatifs aux niveaux environnemental et social (notamment celles prévues dans la composante 3), si des mesures adéquates ne sont pas prises au préalable. Afin de minimiser ces effets défavorables, il a été requis l’élaboration de la présente Evaluation Environnementale et Sociale (EES).
    Description: Commission Sous Régionale des Pêches (CSRP)
    Description: Published
    Description: ressource marine, ressource côtière, politique de pêhce, environnement, qualité des produits, pollution, gestion des pêches,aire marine protégée
    Keywords: Marine resources ; Fisheries ; Fishery management ; Coastal fisheries ; Quality assurance ; Environment management ; Marine resources ; Fisheries ; Fishery management ; Coastal fisheries ; Coastal zone ; Fishery regulations ; Fishery economics ; Marine pollution ; Quality control ; Illegal fishing ; Fishery organizations ; Quality assurance
    Repository Name: AquaDocs
    Type: Report
    Format: 111
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 10
    facet.materialart.
    Unknown
    Suivi de l’activité de la pêche hauturière dans le gouvernorat de Medenine (sud de la Tunisie). (2013)
    INSTM, Institut national des sciences et technologies de la mer | Tunis
    Details
    Publication Date: 2021-05-19
    Description: Ce travail représente une contribution à l'étude de l'activité de pêche hauturière dans le gouvernorat de Médenine, particulièrement, au niveau du port de Zarzis ; durant la période (juin 2005-juin 2006). Il consiste à réaliser, grâce à des enquêtes menées au port, deux types d'analyses : une analyse quantitative afin de déterminer les débarquements saisonniers moyens des espèces les plus débarquées par la pêche hauturière et une analyse qualitative pour établir les structures démographiques des espèces les plus exploitées dans la région. Les résultats obtenus ont montré que, durant la période d'étude, les principales espèces débarquées par la pêche hauturière sont la sardinelle, le maquereau, le saurel, le rouget blanc, le pageot, la thonine, la seiche et la crevette royale. En examinant les débarquements saisonniers moyens des espèces les plus débarquées par type de pêche, nous avons remarqué que deux ou trois espèces dominent pour chaque saison. De plus, l'analyse des structures démographique des apports a montré que la majorité des individus débarqués sont matures, à l’exception du maquereau dont les captures sont constituées d’individus immatures, surtout pendant les saisons d’été et d’automne.
    Description: This work represents a contribution to the study of the offshore fishing activity in the governorate of Medenine, particularly at the port of Zarzis, during the period (june 2005-june 2006. It is to realize, through surveys conducted at the port, two types of analyzes: a quantitative analysis to determine the average seasonal landings of most landed species by fishing offshore units and qualitative analysis to determine the demographic structure of the most exploited species in the region. The obtained results showed that during the period of study, the main landed species by offshore fishing are sardinella, mackerel, horse mackerel, white mullet, sea bream, skipjack tuna, cuttlefish and the caramote prawn. By examining the average seasonal landings of the most landed species, we noticed that, for each season, two or three species dominate. Furthermore, analysis of demographic structures of the landings showed that the majority of landed individuals are mature, with the exception of mackerel catches which are composed of immature individuals, especially during the seasons of summer and autumn.
    Description: Published
    Description: analyse qualitative
    Description: pêche hauturière
    Keywords: Quality analysis ; Offshore ; Fisheries
    Repository Name: AquaDocs
    Type: Proceedings Paper , Refereed , Meeting abstract
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 11
    facet.materialart.
    Unknown
    Técnicas de elaboración y "Curado" de cuerdas de Currican para la pesca en Taganga/Santa Marta, Colombia (2011)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: El presente artículo da una descripción detallada de la elaboración y del "curado" de cuerdas de curricán, utilizadas anteriormente para la pesca en Taganga, un pueblo pescador en la costa norte de Colombia. Antes del "curado", estas cuerdas de fibras de algodón y de fabricación industrial, eran o destorcidas o torcidas a mano nuevamente, o tensionadas y envueltas con una cuerda más delgada del mismo material. El "curado" que siguió a estas operaciones se efectuó tanto en una cocción de corteza de las raíces zanconas de mangle, y/o por medio de un frote de estas cuerdas con los hypocotylos del mismo árbol (Rhizophora manglr). Por medio de las técnicas aquí descritas, los pescadores aspiraban a aumentar la resistencia de sus aparejos de pesca en el agua de mar.
    Description: The present paper gives a detailed description of the elaboration and curing of curricán Unes, formerly used as fishing lines in Taganga, a small fishing village on the northem coast of Colombia. These lines, made of cotton fibers and produced industrially, were disassembled and then retwisted by hand, or tightened and then carefully covered with a thinner string of the same material. The curing {"curado") that followed these operations was achieved by immersion of the lines into a boiled infusión of the bark of the prop roots of mangroves (Rhizophora mangle) and/or a rinsing with the hypocotyls of the same trees. By means of the techniques mentioned, the fishermen sought to improve the resistance of their fishing gear to sea water.
    Description: Published
    Keywords: Fisheries ; Fishing ; Gear construction ; Fisheries ; Fishing
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 12
    facet.materialart.
    Unknown
    Observations on the biology of the redlip Blenny, Ophioblennius atlanticus (Pisces: Blenniidae) on the Colombian Coast of the Caribbean (2011)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: During a 3 week study, a total of 55 individuals of the redlip blenny (Ophioblennius atlanticus) were observed for at least two 15-minute periods, and several for ten of such periods. The sizes of their territories were estimated, the color pattern of each specimen an intra and interspecific interactions were recorded. The mean territory size of the redlip blenny in the study area appeared to be greater than that of these blennies studied in Curacao and Barbados by NURSALL (1977), the difference reflecting perhaps different methods of identifying the territories or a lower density of O. atlanticus in the Santa Marta área. Territories did not appear to be as consistently defended at the study area as at Barbados/Curacao and our impression ¡s that individuals holding large territories are less likely to defend their borders. It seems possible that light colored individuals are protected by their coloration from attack by dark colored territory owners. In territorial defense the redlip blennies grabbed each other tighthy by the mouth and struggled in this position repeatedly for about 15 seconds. Interspecific antagonism was common in the present study, the redlip blennics defended their territory frequently against Eupomacentrus dorsopunicans or E. partitus.
    Description: Durante un estudio de tres semanas, un total de 5 i individuos del bií'nido Ojih'toblcnnius atlnniicur. fueron observados por lo menos durante dos períodos de 1 í minutos para cada individuo y en algunos casos hasta por 10 de estos periodos. Se estimó el área de sus respectivos territorios y se tomó notí de los patrones de coloración de cada espécimen y de las relaciones intra e interespecificas de ellos. El tamaño promedio del territorio de estos blénidos resultó ser mayor que el de los respectivos territorios estudiados por NURSALL (1977) en Curacao y Barbados. Esta diferencia posiblemente se debe a un método diferente de definir los territorios o refleja una densidad menor de la población de O. aílanticus en Santa Marta, Los territorios del área fueron defendidos con menor intensidad a como lo fueron los de Barbados/ Curacao y es nuestra impresión que individuos ocupando un territorio extenso tienden a defender sus límites en menor grado. El color claro de algunos individuos probablemente los protege de agresiones por parte de individuos de color oscuro. En el acto de defensa territorial intraespecífica, los blénidos se agarran por sus bocas y se sacuden mutuamente durante aproximadamente 15 segundos , pudiéndose repetir esti varias veces. Con frecuencia se observarondefensas de los territorios dirigidas hacia los peces doncella Eupomacentrus dorsopunicnas y E. partitus.
    Description: Published
    Keywords: Fisheries ; Biology ; Fisheries ; Biology
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 13
    facet.materialart.
    Unknown
    Primer registro de albinismo en la Familia Muraenesocidae (Pisces: Anguilliformes), Cynoponticus savanna (Bancroft) (2011)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: Se registra por primera vez el fenómeno de albinismo en la familia de peces Muraenesocidae, con base en dos ejemplares de Cynoponticits savanna capturados en la Península de la Guajira. Caribe colombiano.
    Description: The phenomenom of albinism is reported for the first time in che fish family Muraenesocidae. Two anomalous individuals of Cynoponticus savanna were collected from the Guajira Península colombian Caribbean.
    Description: Published
    Keywords: Fisheries ; Albinism ; Fisheries ; Albinism ; New records
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 14
    facet.materialart.
    Unknown
    Las pesquerías con nasas de placer, tranques y chinchorros (2013)
    Details
    Publication Date: 2021-05-19
    Description: Se muestran las capturas históricas de la biajaiba (1935-2000), la evolución de las capturas del pargo (una de las especies de mayor interés económico en Cuba). Se evalúa la utilización de éstas artes de pesca en especies comerciales y su implicación con daños al medio ambiente. Se tiene en cuenta que los pargos criollos, la biajaiba y el caballerote representan el 20 % de las capturas.
    Description: Published
    Description: pesquería artesanal
    Description: cubera
    Description: cherna criolla
    Description: pesca del alto
    Description: pargo
    Description: rabirrubia
    Description: caballerote
    Description: biajaiba
    Keywords: Fisheries ; Artisanal fishing
    Repository Name: AquaDocs
    Type: Journal Contribution , Non-Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 15
    facet.materialart.
    Unknown
    The condition factor of Mugil incilis Hancock (Pisces: Mugilidae) and its seasonal changes in the Cienaga Grande de Santa Marta (Colombia) (2011)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: Se ha estudiado la variación anual de la condición de la lisa Mugil incilis Hancock en la Ciénaga Grande de Santa Marta (CGSM), la mayor laguna costera del Caribe Colombiano, haciendo énfasis en la influencia ejercida por factores ambientales como la salinidad, la temperatura y la transparencia de las aguas sobre la condición de esta especie de Mugilidae. Las diferencias estacionales observadas en la condición de M. incilis están evidentemente relacionadas con su desarrollo gonadal y dependen de la disponibilidad de alimento. La dieta de M. incilis se basa en detritos y su suministro de alimento parece ser muy afectado por el aporte fluvial a la CGSM, el cual es también responsable de los cambios en la salinidad de la laguna, esto explica la relación inversa (r = -0.82) hallada entre la salinidad y la condición de M. incilis expresada por C = 0.9949 - 0.0057 S(°/oo). La variación anual de la salinidad sigue un patrón rítmico de cambios estacionales, no precisamente "in situ", sino en regiones continentales distantes: las cabeceras de los tributarios de la CGSM. Estas lisas desovan en aguas del Caribe adyacente a la CGSM y su período de migración (dic-marzo) comienza con su mejor condición física, y retornan a sus áreas de alimentación en la CGSM 2 a 4 semanas después, hasta el final de la migración, con su condición mínima ya que al parecer estas lisas no se alimentan durante su migración de desove. No se observaron cambios relacionados con las variaciones de la temperatura. Las aguas más turbias coincidieron con los sitios de alimentación de M. incilis.
    Description: The annual variation in condition of the mullet Mugil incilis Hancock has been studied in the Ciénaga Grande de Santa Marta (CGSM). The largest coastal lagoon on the Colombian Caribbean, with emphasis on the influence of such environmental factors as salinity, temperature and transparence of the waters on the condition of this species of Mugilidae. Seasonal differences observed in condition of M. incilis are evidently related to gonadal development and depend on food availability. The diet of M, incilis is based on detritus and its food supply seems to be very influenced by river discharge which also accounts for the salinity changes in the lagoon. this explains the in verse correlation (r = -0.82) found between salinity and condition of the mullets expressed as C = 0.9949 - 0.0057 S (°/oo). Annual salinity variation follows a rhythmic pattern of seasonal changes. not precisely "in situ", but in distant continental regions: the headwaters of the tributarles of the CGSM. These mullets spawn in Caribbean waters adjacent to the CGSM and their migración period (Dec-March) begins with their best physical condición, returning to their feeding áreas in the CGSM 2 or 4 weeks lacer, until the end of the migración, with their lowest condition since these mullets apparently do not feed at all during the spawning migration. No change related to temperature variations was observed. and turbid waters were the rule in M. incilis feeding sites.
    Description: Published
    Description: Mugil incilis
    Keywords: Fisheries ; Estuaries ; Ecology ; Coastal lagoons ; Fishery biology ; Fisheries ; Coastal lagoons ; Estuaries ; Fishery biology ; Ecology
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 16
    facet.materialart.
    Unknown
    Historical development of Cuban fisheries: why we need an integrated approach to fisheries management? (2013)
    Gulf and Caribbean Fisheries Institute
    Details
    Publication Date: 2021-05-19
    Description: Un análisis de los datos arqueológicos e históricos sobre la pesca en Cuba muestra que el impacto de la población aborigen sobre los recursos pesqueros no fue significativo debido a su baja densidad poblacional y a las tecnologías de pesca. El interés por el oro, el tamaño de la población, las limitaciones tecnológicas para la pesca y preservación de las capturas así como las preferencias dietéticas de los españoles todas indican que la pesca tampoco fue una actividad económica importante durante los tres siglos que siguieron a la llegada de Colón. Las preferencias por la carne de res y el bacalao salado y la baja tasa de crecimiento poblacional durante el período colonial determinaron que la mayor parte de los recursos pesqueros, con la excepción del manatí y las tortugas marinas, permanecieran prácticamente inexplorados durante varios siglos después de la Conquista. Los datos estadísticos e históricos revelan que la pesca experimentó un rápido crecimiento desde 1950 y este patrón parece ser una característica común en el Caribe así como en otras partes del mundo. Las presiones sobre la vida marina fueron más evidentes en la segunda mitad del siglo xx cuando el crecimiento poblacional, las mejoras tecnológicas y las demandas del mercado aceleraron el sector pesquero así como la urbanización en la mayoría de los países del caribe.
    Description: Published
    Keywords: Integrated management ; Fisheries
    Repository Name: AquaDocs
    Type: Proceedings Paper , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 17
    facet.materialart.
    Unknown
    Contribución al conocimiento de parasitos de peces de la Ciénaga Grande de Santa Marta I. Familia Acanthocolpidae (Trematoda: Digenea) (2011)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: Se describen y se ilustran seis especies de parásitos pertenecientes a la familia Acanthocolpidae encontradas en 19 especies de peces en su mayoría de considerable importancia económica. El estudio taxonómico de estos parásitos se realizó en la Ciénaga Grande de Santa Marta, al norte de Colombia, desde Enero de 1978 hasta Junio de 1979.
    Description: A taxonomic study for parasites found in 19 mostly economically important fish species was carried out in ihe Ciénaga Grande de Santa Marta (Northern Colombia) from January 1978 uritil June 1979. Six species of fish parasites belonging to the family Acanthocolpidae are described and illustrated herein.
    Description: Published
    Keywords: Fisheries ; Ecology ; Parasites ; Parasites ; Fisheries ; Ecology
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 18
    facet.materialart.
    Unknown
    Aspectos biológicos del Calamar Argentino Illex argentinus (Castellanos) capturado por la flota cubana de pesca en el talud patagónico durante 1987 (2010)
    Santa Marta (Colombia), INVEMAR
    Details
    Publication Date: 2021-05-19
    Description: En 1987, se inicia un programa de muestreos biológicos del calamar argentino ///ex argentinas a bordo de barcos comerciales de la flota cubana de pesca que operan en la plataforma patagónica. La talla de los organismos para ambos sexos presenta un comportamiento estratificado por profundidades, los ejemplares de mayor tamaño se encuentran a profundidades superiores y viceversa, lo cual se ajusta a una recta de regresión (r2 = 0.88; a = 0.05). Las hembras alcanzaron largos promedio del manto superior a los machos, incrementándose la presencia de machos en las capturas desde enero a abril. Se estimaron los largos promedio de primera maduración, como 20.5 y 26.5 cm de largo del manto para machos y hembras respectivamente. Se observó un aumento de la proporción de individuos maduros de febrero a abril, haciéndose más marcado este fenómeno en los machos, que en su mayoría presentaban abundantes espermatóforos en el saco. Se obtuvo la relación largo-peso para hembras y machos y para la combinación de ambos sexos.
    Description: In 1987 a program for the biological sampling of squid ///ex argentinas, was begun on board of a fishing ship belonging to the Cuban Fisheries-Fleet, wich operates in the Patagonian Shelf. The lengths of both sexes presented a estratified pattern with individuals of larger size found in higher depths and viceversa; this pattern is adjusted to a regression line (r2 = 0.88; a = 0.05). Pernales reached average length larger (han males and the rate of males in catches increased from january to april. The first maturation average length was estimated about 20.5 cm for males and 26.5 cm for females. An increase of the rate of mature individuals was observed between february and april emphazasing ¡n males which showed abundant espermatophores in the sac.
    Description: Published
    Description: squid, Flota Cubana
    Keywords: Fisheries ; Squid culture ; Biological charts ; Biological data ; Fisheries ; Squid culture
    Repository Name: AquaDocs
    Type: Journal Contribution
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 19
    facet.materialart.
    Unknown
    The differential effects of changing management regimes on yields from two fisheries exploiting the same resources (2013)
    Details
    Publication Date: 2021-05-19
    Description: A yield per recruit model has been used to compare the effects of mesh size increment on the yields and revenues of the fisheries of Cameroon under two different cases. Case 1 assumes the commercial fishery to move from the exploitation of three age-groups to two age-groups with no interactions with the artisanal fishery, whereas Case 2 takes into account these interactions. The difference in the percentage increase of yield per recruit between case 1 and case 2 is 61% at current fishing (46% and 18% yield per recruit increment in cases 1 and 2 respectively). The usually accepted long-term yield per recruit increment with increase of age at first capture (with a single non-interacting fisheries) is, in this case, cancelled out. However, the revenues increase by 72% and 63% in cases 1 and 2 respectively. Therefore the economic approach, compared with purely biological analyses, is more convincing. In general, as fisheries always interact, a single-fishery management approach should not be the rule as it is at present; management strategies should consider interactions between different fisheries and be based on their economic performances and not, as said earlier, on purely biological considerations. This is because a biological approach to fisheries management will, at best, be modified by economic factors, or, at worst, be ignored totally in favour of economic policies.
    Description: Published
    Keywords: Biology ; Fisheries ; Biological interaction ; Sciaenidae ; Fisheries development ; Fishery management ; Yield/recruit ; Commercial fisheries ; Artisanal fishing
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 20
    facet.materialart.
    Unknown
    Quelles stratégies de suivi, contrôle et surveillance des ressources halieutiques en cogestion locale ? Etude de cas: la surveillance participative au niveau des sites pilotes du programme GIRMaC (2013)
    Details
    Publication Date: 2021-05-19
    Description: La pêche au Sénégal joue un rôle économique et social très important par une contribution globale de près de 11% du PIB primaire et 2,3% du PIB total. Elle occupe de façon directe et indirecte environ 600 000 personnes, soit près de 17% de la population active selon la DP M. Cependant ces dernières décennies, les études ont montré que le secteur traverse une crise aiguë se traduisant par une raréfaction croissante des ressources, notamment les espèces nobles qui ont une forte valeur commerciale. Cette crise est due entre autres à une surexploitation de ces ressources qui est le résultat d’un manque de maîtrise de l’effort de pêche surtout pour les pêcheries artisanales (80% des débarquements et plus de 60% des approvisionnements des industries de la place) au regard du volume de ressources disponibles. Ce manque de maîtrise est dû essentiellement par un défaut du suivi contrôle et surveillance au niveau de la pêche artisanale par l’Etat, qui n’a pas les moyens humains et matériels pour appliquer des mesures de gestion, qui pour la plupart ne sont pas adaptées aux réalités des acteurs à la base. L’objet de cette étude est d’analyser une nouvelle approche axée sur la surveillance participative basée sur l’émergence d’initiatives locales de cogestion au niveau des quatre (04) sites du programme GIRMaC que sont ; Ouakam, Ngaparou, Foundiougne et Bétenty. Il ressort de cette étude que : • Le secteur de la pêche traverse une crise aiguë due principalement selon les acteurs à un défaut de suivi, contrôle et surveillance tel que appliqué actuellement ; • L’approche de cogestion avec des bases juridiques cohérentes, comme le propose le programme GIRMaC peut être un moyen viable pour solutionner à la crise que traverse la pêche ; • D’une part le système Suivi Contrôle et Surveillance coûte cher, d’autre part que ces coûts sont fortement amoindris lorsque les acteurs participent à l’effort de surveillance, par une démarche de surveillance participative en cogestion.
    Description: Président : Omar Thiom THIAW, Professeur UCAD Membres : • Niokhor DIOUF, Chercheur IUPA. • Luis Tito Morais, Chercheur IRD Dakar. • Djiby THIAM, Chercheur GIRMac
    Description: Published
    Description: surveillance; contrôle; cogestion; effort de pêche; pêcherie; surexploitation; biodiversité; pêche artisanale
    Keywords: Ocean surveillance ; Ecosystem management ; Fishing effort ; Overexploitation ; Biodiversity ; Artisanal fishing ; Fisheries
    Repository Name: AquaDocs
    Type: Theses and Dissertations , Master thesis
    Format: 87
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 21
    facet.materialart.
    Unknown
    Report of the EAF REGIONAL TASK GROUP MEETING AND ECOLOGICAL RISK ASSESSMENT METHODOLOGY WORKSHOP (SOUTH WEST INDIAN OCEAN) (2014)
    FAO | Rome
    Details
    Publication Date: 2021-01-30
    Description: The first meeting of the South West Indian Ocean EAF Regional Task Group (RTG) was held in Mombasa, Kenya, from 27 to 30 January 2009, together with an ecological risk assessment methodology workshop. It was attended by 20 partic ipants from the South West Indian Ocean (SWIO) countries, the South West Indian Ocean Fisheries Project (SWIOFP), the Agulhas and Somali Currents Large Marine Ecosystems (ASCLME) project, the Scientific Committee of the South West Indian Ocean Fisheries Commission, the United Nations Environment Programme (UNEP)/Nairobi Convention Implementation Unit, the African Union Commission and FAO. The RTG is an implementation structure under the EAF-Nansen project GCP/INT/003/NOR and serves as the forum for training in ecological risk assessment that is the methodology used for the identification and prioritization of issues requiring management attention. The main objectives of the meeting and workshop we re to discuss and facilitate key processes and activities for the implementation of the ecosystem approach to fisheries management in the South West Indian Ocean region including the modalities for the formation and functioning of the RTG and National Task Groups (NTGs). It was explained that, to be able to achieve the objectives of implementing an ecosystem approach to fisheries at the national level, certain key structures have to be in place including the NTG with representatives of key stakeholders in a given fishery and that would take the lead in the process. An overview of the key concepts and process of the ecological risk assessment methodology were clarified. Participants were also introduced to the preparation of EAF baseline reports to be used as initial input for the work on ecosystems approach to fisheries. It was explained that the preparation of the report is to be led by national and regional experts and overseen by the NTG. For the exercises the participants worked in three subgroups formed during the meeting with each group selecting a chairman who moderate d the discussions and a rapporteur. The participants expressed satisfaction with the development of a communication strategy for the project and especially with the participatory approach used.
    Description: FAO, NORAD, Institute of Marine Research
    Description: Published
    Description: National task groups
    Description: Regional task groups
    Description: Ecosystem Approach to Fisheries
    Keywords: Ecosystems ; Fisheries ; Ecosystems ; Fishery resources ; Fisheries management
    Repository Name: AquaDocs
    Type: Report , Non-Refereed
    Format: 36
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 22
    facet.materialart.
    Unknown
    Déscription de l'activité ds flotilles pélagiques industrielles en 1986 dans la ZEEM mauritanienne (2013)
    Details
    Publication Date: 2021-05-19
    Description: Published
    Description: espéces pélagiques
    Description: sardine
    Description: pêche industrielle
    Keywords: Fisheries ; Pelagic fisheries ; Industrial fish ; Fish products ; Fishing industry ; Fishing fleet
    Repository Name: AquaDocs
    Type: Journal Contribution , Non-Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 23
    facet.materialart.
    Unknown
    NIOMR Newsletter, Jan-Jun 2010. (2014)
    Nigerian Institute for Oceanography and Marine Research | Lagos, Nigeria
    Details
    Publication Date: 2021-01-30
    Description: Published
    Description: Fisheries newsletter
    Keywords: Fisheries ; Marine sciences ; Fisheries literature
    Repository Name: AquaDocs
    Type: Report , Non-Refereed
    Format: 30pp.
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 24
    facet.materialart.
    Unknown
    NIOMR Newsletter, Jan-Jun 2012. (2014)
    Nigerian Institute for Oceanography and Marine Research | Lagos, Nigeria
    Details
    Publication Date: 2021-01-30
    Description: Published
    Description: Fisheries newsletter
    Keywords: Fisheries ; Marine sciences ; Fisheries literature
    Repository Name: AquaDocs
    Type: Report , Non-Refereed
    Format: 34pp.
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 25
    facet.materialart.
    Unknown
    NIOMR Newsletter, Jan-Apr 2009. (2014)
    Nigerian Institute for Oceanography and Marine Research | Lagos, Nigeria,
    Details
    Publication Date: 2021-01-30
    Description: Published
    Description: Fisheries newsletter
    Keywords: Fisheries ; Fisheries literature
    Repository Name: AquaDocs
    Type: Report , Non-Refereed
    Format: 11pp.
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 26
    facet.materialart.
    Unknown
    Chaine froide dans la conservation du poisson (2013)
    Details
    Publication Date: 2021-05-19
    Description: Unpublished
    Description: conservation
    Description: chaine froide
    Description: poisson
    Keywords: Food conservation ; Fisheries ; Fish conversion ; Conservation (fishery products) ; Glass ; Fisheries
    Repository Name: AquaDocs
    Type: Journal Contribution , Non-Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 27
    facet.materialart.
    Unknown
    La pêche des senneurs dans la Baie du Lévrier en 1971 (2013)
    Details
    Publication Date: 2021-05-19
    Description: Published
    Description: Pêche
    Description: Senneur
    Keywords: Seining ; Fisheries ; Fisheries ; Seiners
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 28
    facet.materialart.
    Unknown
    Etat des lieux de la filière de transformation artisanale des produits halieutiques au Sénégal (2013)
    Details
    Publication Date: 2021-05-19
    Description: ACDI;CRDI; République Française, Ministère des Affaires Etrangéres; CDE; Enda Graf Sahel;
    Description: Conseil Info MPEA, Projer d'Accés à l'information et au Conseil pour les microet petites entreprises agroalimentaires; Projet d'Appui aux Opérateurs/trices de l'Agroalimentaires (PAOA); Cintech Agroalimentaire; Groupe de Recherche et d'Echanges Technologiques (GRET); Enda GRaf Sahel; SNC-LAVALIN International
    Description: Published
    Description: transformation; transformation artisanale; échantillonage; collecte de données; commercialisation
    Keywords: Processing fishery products ; Biological sampling ; Data collections ; Marketing and distribution ; Fisheries
    Repository Name: AquaDocs
    Type: Theses and Dissertations , Master thesis
    Format: 41
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 29
    facet.materialart.
    Unknown
    Pêcherie démersale côtière au Sénégal. Essai de modélisation de la dynamique de l'exploitation des stocks (2013)
    Details
    Publication Date: 2021-05-19
    Description: Français - Les traits essentiels de la côte sénégalaise, repères historiques de la pêche, communautés de pêcheurs, caractéristiques des flottes et modes d’accès à la ressource et d’interaction sont analysés. Les caractéristiques, tendances décroissantes de l’abondance,niveaux d’exploitation, mesures d’aménagement, relations interspécifiques, changements potentiels et sources de variation des stocks démersaux côtiers sont précisés. Les notions de tactiques et stratégies de pêche sont passées en revue, conceptualisées puis étudiées.Le modèle «Dynamique Conjointe Exploitation Ressource» utilisé repose sur la définition de 4 typologies. L’utilisation de méthodes de classification et de connaissances d’experts conduit à considérer 32 stocks, 31 strates, 82 tactiques et 25 flottilles artisanales et chalutières. Les typologies sont articulées avec la prise en compte de paramètres relatifs à l’économie, aux stocks, flottilles et règles de décisions. L’ajustement est satisfaisant en partie. Toutefois, le modèle garde son importance en matière de prospective et d’objectifs à atteindre via la définition de variables de contrôle. Notre travail peut être considéré comme une esquisse invitant à un groupe de travail élargi aux experts des institutions halieutiques nationales voire, sous-régionales. Des propositions sont faites sur les bases de données, les licences de pêche et l’étude des tactiques et stratégies à mener suivant des pas de temps raisonnables pour tenir compte du grand dynamisme des pêcheries. Dès lors qu'il s’agit de caractériser l'impact de la pêche sur l'écosystème, ces travaux sont des éléments essentiels des recherches à faire sur la dynamique des écosystèmes exploités. English - The essential features of the Senegalese coast, fisheries history, fishermen's communities, artisanal and trawling fleet’s characteristics and their way of accessing to the resource and interactions are described. The characteristics, evolutionary tendencies of abundance, level of exploitation, measures of fisheries management, interspecific relationship, potential evolutionary changes and sources of variation of coastal demersal stocks are specified. Tactics and strategies are reviewed, conceptualized and studied. We used the model "Dynamique Conjointe Exploitation Ressource" which lies on 32 stocks, 31 strata, 82 tactics, 25 fleets and several other parameters dealing with stocks, fleets, economy and making decision rules. The adjustment is partially satisfactory but the model is of great interest for prospective studies and objectives to reach once defined variables of control. Our work is an outline calling for an enlarged working group implying national or sub regional fisheries institutional experts. Tactics and strategies studies, re-actualized in artisanal fisheries, are performed for the first time in industrial fisheries. The typological approach is simple, pertinent, efficacy and fast. Propositions are made relatively to databases, fishing licenses and tactics and strategies studies that should be implemented according to a reasonable time steps in order to take into account the big dynamism of the Senegalese fisheries. As it is intended to characterize fisheries impact on ecosystem, these works are one of essential research elements on the dynamic of exploited ecosystems.
    Description: Published
    Description: pêcherie; démersale côtière; modélisation; stocks; écosystème; communauté de pêcheurs; eaux continentales; eaux marines; saison hydrologique; pêcheur; flottille; crevettier; capture; aménagement des pêcheries; pêche chalutière; pêche artisanale; licence de pêche; permis de pêche
    Keywords: Fisheries ; Demersal fisheries ; Modelling ; Stocks ; Ecosystems ; Community fishing ; Inland waters ; Marine water ; Hydrologic cycle ; Fishermen ; Fishing fleet ; Shrimp fisheries ; Capture fisheries ; Fisheries management ; Trawling ; Artisanal fishing ; Fishing licenses
    Repository Name: AquaDocs
    Type: Theses and Dissertations , Bachelor thesis
    Format: 234
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 30
    facet.materialart.
    Unknown
    Etude sur le savoir écologique des pêcheurs artisans des petits pélagiques en Afrique du Nord-Ouest (2010)
    Details
    Publication Date: 2021-05-19
    Description: Agriculture, Nature and Food Quality, Den Haag (Netherlands); Ministerie Van Buitenlandse Zaken, Brussel (Belgium); Wageningen International, Wageningen (Netherlands)
    Description: Projet BBI 13286 : Pêche durable des petits pélagiques en Afrique Nord Ouest Ce rapport a été préparé avec le soutien financier de la Coopération néerlandaise (DGIS) dans le cadre de son Programme de politique internationale en matière de biodiversité (BBI).
    Description: Published
    Description: pêche traditionnelle; taille; échantillonnage; écosystème; upwelling; biomasse; filet maillant dérivant; senne tournante; senne moustiquaire; senne de plage; maquereau; chinchard; sardinelle; ethmalose; reproduction; courant; stocks; réglementation; pêche par espéce; engin de pêche; pélagique; zone côtière; pirogue; pêche artisanale; pêcheur
    Keywords: Biomass ; Ecosystems ; Fisheries ; Fishermen ; Stocks ; Ocean currents ; Winds ; Size ; Fishing effort ; Pelagic fisheries ; Sexual reproduction ; Multispecies fisheries ; Fisheries ; Artisanal fishing ; Fishermen ; Fishing effort ; Canoe fisheries ; Coastal zone ; Fishery engineering ; Protected resources ; Pelagic fisheries ; Cycles ; Sexual reproduction ; Multispecies fisheries ; Stocks ; Ocean currents ; Winds ; Biomass ; Upwelling ; Ecosystems ; Maritime legislation ; Size
    Repository Name: AquaDocs
    Type: Report
    Format: 53
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 31
    facet.materialart.
    Unknown
    Traitement traditionnel et conservation des produits de la pêche en Mauritanie (2013)
    Details
    Publication Date: 2021-05-19
    Description: Published
    Description: conservation
    Description: produits
    Description: pêche
    Keywords: Conservation ; Fisheries ; Fish products
    Repository Name: AquaDocs
    Type: Journal Contribution , Non-Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 32
    facet.materialart.
    Unknown
    NIOMR Newsletter, May-Oct 2009. (2014)
    Nigerian Institute for Oceanography and Marine Research, | Lagos, Nigeria,
    Details
    Publication Date: 2021-01-30
    Description: Published
    Description: Fisheries newsletter
    Keywords: Fisheries ; Fisheries literature
    Repository Name: AquaDocs
    Type: Report , Non-Refereed
    Format: 8pp.
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 33
    facet.materialart.
    Unknown
    Projet d'aménagement des stocks pélagiques partagés : Cas des pêcheries de mulets et de courbines en Mauritanie et au Sénégal (2011)
    Details
    Publication Date: 2021-01-30
    Description: En Afrique de l'Ouest, la zone littorale et ses ressources représentent une composante essentielle pour le développement. Près de 60% de la population est concentrée à moins de 20 km des côtes . La part des ressources halieutiques dans l'alimentation des populations est très importante et croissante. Au Sénégal par exemple, elles contribuent jusqu'à 70% des apports en protéines. A cela s'ajoute le poids socio-économique très important de la pêche en général et de la pêche artisanale en particulier devenue l'un des secteurs les plus stratégiques pour l'économie nationale en Mauritanie notamment. Le Cadre Stratégique de Lutte contre la Pauvreté du Gouvernement Mauritanien considère que : "compte tenu des possibilités qu'elle offre en terme de création d'emplois et de sécurité alimentaire notamment pour les populations pauvres, mais également de génération de recettes en devises, la pêche artisanale revêt une grande priorité, un plan décennal de développement lui sera consacré ".
    Description: Published
    Description: pêche artisanale; littoral; carpe; ethmalose; donnée; mulet; pélagique; pourtague; stock halieutique; pêche; communauté de pêcheurs; effort de pêche; PNBA; technique de pêche; senne tournante; sardinelle; gonade; filet de pêche; courbine; migration d'espèces; campagne de pêche; écosystème; dégradation d'habitats de poissons; enjeux socioéconomiques; commercialisation; conservation
    Keywords: Fisheries ; Fishermen ; Stocks ; Fish fillets ; Ecosystems ; Fishing effort ; Pelagic fisheries ; Artisanal fishing ; Fisheries ; Fishermen ; Stocks ; Capture fishery economics ; Fish eggs ; Fish fillets ; Fishing effort ; Fishery technology ; Mullet fisheries ; Pelagic fisheries ; Ecosystems
    Repository Name: AquaDocs
    Type: Report
    Format: 6
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 34
    facet.materialart.
    Unknown
    Aquaculture and capture fisheries : a conceptual approach toward an integrated economic-ecological analysis (2012)
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © The Author(s), 2012. This is the author's version of the work. It is posted here by permission of Taylor & Francis for personal use, not for redistribution. The definitive version was published in Aquaculture Economics & Management 16 (2012): 167-181, doi:10.1080/13657305.2012.678551.
    Description: This study presents a framework for analyzing the interactions between aquaculture and capture fisheries in the context of ecosystem-based management. We extend a model of the economic and ecological systems in coastal New England by incorporating an aquaculture sector in a computable general equilibrium (CGE) model and by examining the forage fish and aquaculture link in a marine food web. We show that aquaculture and commercial fisheries interact in a complex way throughout the economic and ecological systems.
    Description: This work was supported by the NOAA Saltonstall-Kennedy Grant Program (Award No. NA09NMF4270097), the MIT Sea Grant College Program (NOAA Award No. NA10OAR4170086, Subaward No. 5710002974), and the Johnson Endowment of the WHOI Marine Policy Center.
    Description: 2013-06-08
    Keywords: Aquaculture ; Fisheries ; Ecosystem-based management ; CGE model ; Food web model ; Forage fish
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: application/pdf
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 35
    facet.materialart.
    Unknown
    Habitat damage, marine reserves, and the value of spatial management (2013)
    Ecological Society of America
    Details
    Publication Date: 2022-05-25
    Description: Author Posting. © Ecological Society of America, 2013. This article is posted here by permission of Ecological Society of America for personal use, not for redistribution. The definitive version was published in Ecological Applications 23 (2013): 959–971, doi:10.1890/12-0447.1.
    Description: The biological benefits of marine reserves have garnered favor in the conservation community, but “no-take” reserve implementation is complicated by the economic interests of fishery stakeholders. There are now a number of studies examining the conditions under which marine reserves can provide both economic and ecological benefits. A potentially important reality of fishing that these studies overlook is that fishing can damage the habitat of the target stock. Here, we construct an equilibrium bioeconomic model that incorporates this habitat damage and show that the designation of marine reserves, coupled with the implementation of a tax on fishing effort, becomes both biologically and economically favorable as habitat sensitivity increases. We also study the effects of varied degrees of spatial control on fisheries management. Together, our results provide further evidence for the potential monetary and biological value of spatial management, and the possibility of a mutually beneficial resolution to the fisherman–conservationist marine reserve designation dilemma.
    Description: M. G. Neubert acknowledges the support of the National Science Foundation (DMS-0532378, OCE-1031256) and a Thomas B. Wheeler Award for Ocean Science and Society. H. V. Moeller acknowledges support from a National Science Foundation Graduate Research Fellowship. This research is based in part on work supported by Award No. USA 00002 made by King Abdullah University of Science and Technology (KAUST).
    Keywords: Bioeconomics ; Destructive fishing practices ; Fisheries ; Habitat damage ; Marine protected areas ; Marine reserves ; Optimal control ; Optimal harvesting ; Spatial management
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 36
    facet.materialart.
    Unknown
    Projet pour le développement rationnel et durable du secteur de la pêche au Sénégal (INT/07/16M/SPA) (2013)
    Ministerio de Medio Ambiente y Medio Rural y Marino | Madrid (Espagne)
    Details
    Publication Date: 2021-05-19
    Description: Description du secteur de la pêche Avec la Mauritanie, le Sénégal est de loin le plus grand producteur de produits de pêche de la sous région. Avec 718 km de cote et un territoire maritime de 198km2, 15 745 km2 de superficie fluviale, 2 estuaires, des mangroves et un lac de 350km2, le Sénégal possède tous les atouts des plus grands producteurs de pêche. Le potentiel annuel de captures s’élève à 500 000 tonnes. Le secteur a subi une croissance spectaculaire ces trente dernières années : les débarquements sont passés 50 000 tonnes en 1965 à plus de 450 000 en 1997. Le secteur se compose principalement de deux sous-secteurs : la pêche industrielle et la pêche traditionnelle ou artisanale. Cette dernière, vielle de plusieurs siècles a su s’adapter et se moderniser au cours des dernières décennies. La flotte de pêche artisanale est dynamique et diversifiée ; selon les estimations, en 2005 il y avait plus de 13 000 pirogues. La pêche artisanale se concentre dans sept régions maritimes et fluviales du pays: Dakar, Thiès, Saint Louis, Fatick, Zinguinchor, Louga et Kaolack. Le port de Kayar dans la région de Thiès correspond à la principale zone de débarquement de la pêche artisanale avec environ 70% des débarquements. Dans le secteur industriel, les pêcheurs travaillent à bord d’une flottille de petits sardiniers, de 143 chalutiers destinés à la pêche d’espèces demersales, de 3 sardiniers et de 42 thoniers. Alors que le Sénégal domine largement le sous-secteur demersale avec 70% des chalutiers opérants, le pays ne possède que 6 thoniers contre 38 étrangers, dont une partie seulement des captures est débarquée au Sénégal. La pêche industrielle est concentrée autour de la capitale dans le Port autonome de Dakar et des ports secondaires de Saint Louis, Kaolack et Ziguinchor. Aujourd’hui, le secteur de la pêche sénégalaise est largement dominé par la pêche artisanale, qui constituait 90% des cargaisons totales des produits de la mer en 2006 avec 350 000 tonnes. Plus de 60% des produits de la pêche artisanale sont destinés à l’exportation et la transformation. En 2006, le secteur dans son ensemble représentait 9% du PIB du secteur primaire, 1.5% du PIB total, et 1/3 des devises étrangères (250 millions de dollars par an). Plus importante que le poids économique du secteur, est son poids social : la pêche génère indirectement 600 000 emplois, dont 67% au sein du secteur artisanal. En outre, les produits de la pêche comblent les besoins en protéines animales de la population sénégalaise à hauteur de 75%1. La pêche a connu une expansion spectaculaire au cours des dernières décennies grâce à l’impulsion de politiques publiques de développement basées sur une logique sectorielle productiviste. Une flotte nationale artisanale et industrielle a été progressivement mise en place ainsi que de fortes capacités de transformation industrielle. Cet engagement de l’Etat a ensuite connu un net ralentissement du fait, entre autre, des politiques d’ajustement structurel. Le renchérissement des coûts de production subséquents à la dévaluation du franc CFA en 1994 a lourdement affecté les pêcheurs. Parallèlement, avec la forte demande en produits halieutiques et en l’absence de politiques adéquates et cohérentes de gestion durable des ressources exploitables, une situation de surexploitation des ressources halieutiques s’est installée. En conséquence de la raréfaction des ressources halieutiques, la pêche sénégalaise traverse une crise sans précédent, dont les effets commencent à se faire sentir à tous les niveaux : appauvrissement des communautés de pêcheurs, menace de l’approvisionnement en poisson des populations, baisse des captures à haute valeur ajoutée, baisse des exportations, baisse de la rentabilité et des revenus des unités de pêche. Par ailleurs, de plus en plus d’établissements de transformation industrielle ferment (23 entreprises entre 1999 et 2006).
    Description: Ministerio de Medio Ambiente Y Medio Rural y Marino
    Description: Pablo Manuel Xandri Royo CTP Proyecto (INT/07/16M/SPA) Este trabajo se ha realizado en el marco del Convenio de Colaboración entre el actual Ministerio de Medio Ambiente y Medio Rural y Marino de España y la Organización Internacional del Trabajo de 28 de diciembre de 2007
    Description: Published
    Description: environnement; socio-économie; pêche; capture; débarquement; engin de pêche; femme; pêcheur; convention internationale; réglementation
    Keywords: Fisheries ; Marine environment ; Socioeconomic aspects ; Capture fisheries ; Landing statistics ; Fishing gear ; Women ; Fishermen ; Conventions ; Fishery regulations
    Repository Name: AquaDocs
    Type: Report , Non-Refereed
    Format: 208
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 37
    facet.materialart.
    Unknown
    Le secteur des pêches au Sénégal: tendances, enjeux et orientations politiques (2013)
    Programme Kurukan Fugan (Union Européenne/Gouvernement du Sénégal/Enda Graf/Gret) | Dakar (Sénégal)
    Details
    Publication Date: 2021-05-19
    Description: Programme KURUKAN FUGAN (Union Européenne/Gouvernement du Sénégal/EndaGraf/GRET)
    Description: Published
    Description: politique de pêche; environnement marin; socio-économie; co-gestion; aquaculture; pêche artisanale; pêche industrielle; pêcherie; ONG; AMP; ressource halieutique; organisations professionnelles
    Keywords: Marine environment ; Socioeconomic aspects ; Fishery management ; Aquaculture ; Artisanal fishing ; Fisheries ; Industrial fish ; Fishery resources ; Fishing policy ; Protected areas ; Professionals
    Repository Name: AquaDocs
    Type: Book , Non-Refereed , Article
    Format: 26
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 38
    facet.materialart.
    Unknown
    Accord visant à favoriser le respect par les navires de pêche en haute mer des mesures internationales de conservation et de gestion (2011)
    Details
    Publication Date: 2021-01-30
    Description: Ministère des Affaires Etrangères (Sénégal); Ambassade du Sénégal à Rôme (Italy)
    Description: "Action 21"; FAO; application de l'accord; responsabilité de l'état du pavillon; échange d'informations; tiers à l'accord; règlement des différents; adhésion; entrée en vigueur; réserves; amendements; retraits; fonction du dépositaire.
    Keywords: Fisheries ; International agreements ; International cooperation ; Fisheries ; International agreements ; Maritime legislation ; International cooperation
    Repository Name: AquaDocs
    Type: Other
    Format: 14
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 39
    facet.materialart.
    Unknown
    La pesca en Cuba : apuntes para su historia (II) : la pesca desde 1492 hasta 1902 : etapa colonial (2013)
    Details
    Publication Date: 2021-09-18
    Description: En la época colonial algunas especies de peces cubanos retienen sus nombres por los cuales eran conocidos por los aborígenes: biajaca, biajaiba, cojinúa, jiguagua, cibí. Aún hoy se designan de igual forma. En esta época aparece la primera obra científica impresa en Cuba, los primeros pueblos pescadores y los primeros científicos.
    Description: Published
    Keywords: Fisheries
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 40
    facet.materialart.
    Unknown
    La pesca en Cuba : apuntes para su historia (I) : la pesca en las comunidades primitivas : etapa precolombina (2013)
    Details
    Publication Date: 2021-09-18
    Description: Published
    Description: especies nativas
    Description: pesca
    Keywords: Fisheries ; Indigenous species ; Indigenous fishing
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 41
    facet.materialart.
    Unknown
    La pesca en Cuba : apuntes para su historia (III) : la pesca desde 1902 hasta 1952 : etapa de la seudorrepública (2013)
    Details
    Publication Date: 2021-09-18
    Description: Published
    Keywords: Fisheries
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 42
    facet.materialart.
    Unknown
    La Pesca de los peces de pico en Cuba (I) (2013)
    Details
    Publication Date: 2021-09-18
    Description: Recuento en forma breve de las pesquerías de estas especies durante varios siglos, en los cuales los sabios Parra y Felipe Poey ofrecen descripciones. Precios, lugares de captura y pescadores son los protagonistas.
    Description: Published
    Description: Emperador-Xiphias gladius
    Description: pez espada
    Description: castero-Makaira nigricans
    Description: aguja blanca-Tetrapturus albidus
    Keywords: Fisheries ; Fishes
    Repository Name: AquaDocs
    Type: Journal Contribution , Non-Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 43
    facet.materialart.
    Unknown
    La pesca de los peces de pico en Cuba (II). (2013)
    Details
    Publication Date: 2021-09-18
    Description: Causas del descenso en las pesquerías de estas especies a partir de 1975. Se describen las técnicas y artes de pesca empleadas y se abunda en la complejidad de las capturas y las características de los palangres empleados para cada especie. Una comparación es establecida además con países del área. De forma muy didáctica e instructiva.
    Description: Published
    Description: castero-Makaira nigricans
    Description: Emperador-Xiphias gladius
    Description: aguja blanca-Tetrapturus albidus
    Keywords: Fisheries ; Fishes
    Repository Name: AquaDocs
    Type: Journal Contribution , Non-Refereed , Article
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 44
    facet.materialart.
    Unknown
    A review of interactions between cetaceans and fisheries in the Azores (2011)
    Details
    Publication Date: 2022-05-26
    Description: Author Posting. © John Wiley & Sons, 2010. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Aquatic Conservation: Marine and Freshwater Ecosystems 21 (2011): 17-27, doi:10.1002/aqc.1158
    Description: 1. Interactions between cetaceans and fishing activity in the Archipelago of the Azores were examined using information contained in grey literature and previously unpublished data collected by observer programmes and research projects from 1998 to 2006. Together with a brief description of the economics, gear, fishing effort, and past and ongoing monitoring projects, levels of cetacean bycatch and interference were reported for each major fishery. 2. Cetaceans were present in 7% (n=973) and interfered in 3% (n=452) of the fishing events monitored by observers aboard tuna-fishing vessels. Interference resulted in a significantly higher proportion of events with zero catches but it was also associated with higher tuna catches. 3. There was a decreasing trend in the proportion of tuna-fishing events with cetacean presence or interference throughout this study, as well as a reduction in the estimates of dolphins captured annually by the whole fleet. 4. Observers reported cetacean depredation in 16% of the sets for demersal species and in 2% of the sets for swordfish. Cetacean presence and depredation were associated with higher overall catches and higher catches per unit effort in demersal fisheries. Bottlenose dolphins (Tursiops truncatus) were responsible for most depredation events in demersal fisheries, whereas in the swordfish fishery, depredation was associated with the presence of killer whales (Orcinus orca). There were no reports of cetacean bycatch in these fisheries. There were also no reports of cetaceans interacting in the experimental deep-sea fisheries that were examined. 5. Available data suggests that levels of interaction between cetaceans and Azorean fisheries are generally low and that the economic impact of cetacean interference is probably small. However, for several traditional fisheries there are no accurate data to determine levels of cetacean interaction. We recommend that existing observer programmes be expanded to increase observer coverage of the demersal and swordfish fisheries and allow monitoring of other existing and emerging fisheries.
    Description: M.A.S. was supported by an FCT postdoctoral (SFRH/BPD/29841/2006) grant, and R.P. was supported by an FCT doctoral grant (SFRH/BD/32520/2006).
    Keywords: Cetacean–fisheries interactions ; Depredation ; Bycatch ; Fisheries ; Atlantic Ocean ; Azores
    Repository Name: Woods Hole Open Access Server
    Type: Preprint
    Format: application/pdf
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 45
    facet.materialart.
    Unknown
    Multiple genetic stocks of longfin squid Loligo pealeii in the NW Atlantic : stocks segregate inshore in summer, but aggregate offshore in winter (2011)
    Inter-Research
    Details
    Publication Date: 2022-05-26
    Description: Author Posting. © Inter-Research, 2006. This article is posted here by permission of Inter-Research for personal use, not for redistribution. The definitive version was published in Marine Ecology Progress Series 310 (2006): 263-270, doi:10.3354/meps310263.
    Description: The longfin squid Loligo pealeii is distributed widely in the NW Atlantic and is the target of a major fishery. A previous electrophoretic study of L. pealeii was unable to prove genetic differentiation, and the fishery has been managed as a single unit stock. We tested for population structure using 5 microsatellite loci. In early summer (June), when the squids had migrated inshore to spawn, we distinguished 4 genetically distinct stocks between Delaware and Cape Cod (ca. 490 km); a 5th genetic stock occurred in Nova Scotia and a 6th in the northern Gulf of Mexico. One of the summer inshore stocks did not show genetic differentiation from 2 of the winter offshore populations. We suggest that squids from summer locations overwinter in offshore canyons and that winter offshore fishing may affect multiple stocks of the inshore fishery. In spring, squids may segregate by genetic stock as they undertake their inshore migration, indicating an underlying mechanism of subpopulation recognition.
    Description: We acknowledge funding from WHOI Sea Grant NA16RG2273, the Massachusetts Environmental Trust (#98-04), and the Sholley Foundation.
    Keywords: Fisheries ; Spawning migration ; Microsatellites ; Population structure ; Population recognition ; Null alleles
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 46
    facet.materialart.
    Unknown
    Spillover from marine reserves and the replenishment of fished stocks (2010)
    Cambridge University Press
    Details
    Publication Date: 2022-05-26
    Description: Author Posting. © Foundation for Environmental Conservation, 2009. This article is posted here by permission of Cambridge University Press for personal use, not for redistribution. The definitive version was published in Environmental Conservation 36 (2009): 268-276, doi:10.1017/S0376892910000032.
    Description: No-take marine reserves are widely recognized as an effective conservation tool for protecting marine resources. Despite considerable empirical evidence that abundance and biomass of fished species increase within marine reserve boundaries, the potential for reserves to provide fisheries and conservation benefits to adjacent waters remains heavily debated. This paper uses statistical and population models to evaluate published empirical data on adult spillover from marine reserves and shows that spillover is a common phenomenon for species that respond positively to reserve protection, but at relatively small scales, detectable on average up to 800 m from reserve boundaries. At these small scales, local fisheries around reserves were likely unsustainable in 12 of 14 cases without the reserve, and spillover partially or fully offsets losses in catch due to reserve closure in the other two cases. For reserves to play a role in sustaining and replenishing larger-scale fished stocks, networks of reserves may be necessary, but as few exist this is difficult to evaluate. The results suggest reserves can simultaneously meet conservation objectives and benefit local fisheries adjacent to their boundaries.
    Description: Support was provided by a grant from the David and Lucille Packard Foundation to NCEAS for ecosystem-based management ofmarine systems, the Partnership for Interdisciplinary Studies of Coastal Oceans (PISCO) funded by the David and Lucile Packard Foundation and the Gordon and Betty Moore Foundation (contribution number 348), the Sustainable Fisheries Group supported by the Paul G. Allen Family Foundation and the Bahamas Biocomplexity Project (US NSF Biocomplexity grantOCE-0119976) andUS EPA Science to Achieve Results (R832223).
    Keywords: Adult fish movement ; Fisheries ; Global ; Marine protected areas ; No-take reserves ; Spillover effect ; Synthesis
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    PAPER (OA)
  • 47
    Electronic Resource
    Electronic Resource
    Land loss in coastal Louisiana (U.S.A.) (1979)
    Springer
    Environmental management 3 (1979), S. 133-144 
    Details
    ISSN: 1432-1009
    Keywords: Coastal zone Management ; Fisheries ; Marshes ; Wetlands ; Louisiana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract This paper examines causes and consequences of wetland losses in coastal Louisiana. Land loss is a cumulative impact, the result of many impacts both natural and artificial. Natural losses are caused by subsidence, decay of abandoned river deltas, waves, and storms. Artificial losses result from flood-control practices, impoundments, and dredging and subsequent erosion of artificial channels. Wetland loss also results from spoil disposal upon wetlands and land reclamation projects. Total land loss in Louisiana's coastal zone is at least 4,300 ha/year. Some wetlands are converted to spoil banks and other eco-systems so that wetland losses are probably two to three times higher. Annual wetland losses in the Barataria Bay basin are 2.6% of the wetland area. Human activities are the principal determinants of land loss. The present total wetland area directly lost because of canals may be close to 10% if spoil area is included. The interrelationship between hydrology, land, vegetation, substrate, subsidence, and sediment supply are complicated; however, hydrologic units with high canal density are generally associated with higher rates of land loss and the rate may be accelerating. Some cumulative impacts of land loss are increased saltwater intrusion, loss of capacity to buffer the impact of storms, and large additions of nutrients. One measure of the impact is that roughly $8–17 × 106 (U.S.A.) of fisheries products and services are lost annually in Louisiana. Viewed at the level of the hydrologic unit, land loss transcends differences in local vegetation, substrate, geology, and hydrology. Land management should therefore focus at that level of organization. Proper guideline recommendations require an appreciation of the long-term interrelations of the wetland estuarine system.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01867025
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 48
    Electronic Resource
    Electronic Resource
    Production of a fish taxocene in a Texas pond (1977)
    Springer
    Environmental biology of fishes 2 (1977), S. 241-259 
    Details
    ISSN: 1573-5133
    Keywords: Production ; Fisheries ; Population dynamics ; Energetics ; Fishes ; Competition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Synopsis Production rates of seven species of fishes were determined for one year in a 0.95 ha pond. Total annual production of all fishes in the pond was 209 g m−2y−1 (after the subtraction of 16.2 g m−2y−1 of negative production). Over 90% of the production occurred in the months of June through September, with young-of-the-year fishes contributing 84% of the total. When Y of Y fishes shifted to benthic diets in the spring, the small biomass of benthos available could not sustain the large biomas of fish. Severe competition for the available food then resulted in decreased production rates for the entire fish taxocene.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00005993
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 49
    Electronic Resource
    Electronic Resource
    Masthead (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975) 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080101
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 50
    Electronic Resource
    Electronic Resource
    Zur Kenntnis des Narciclasins (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 445-463 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemistry of NariciclasineFrom narciclasine (2a), the acetonide 8a and its oxidation product 10 are prepared. 10 isomerizes easily to give 11. Catalytic hydrogenation of 2a yields a mixture of dihydronarci-clasines from which the pure cis- and trans-isomers 14a and 15a can be obtained via the tetraacetates. As a by-product of the hydrogenation, isonarciclasine (16a) is isolated. The relative configuration of narciclasine (as represented by formula 2a) is established by the n. m. r. spectra of 15b and 16b. Lycoricidine and margetine are shown to be identical; their configuration is as shown in formula 2b. Some biological tests are reported.
    Notes: Aus Narciclasin (2a) wird das Acetonid 8a und dessen Oxidationsprodukt 10 dargestellt. 10 wird leicht zu 11 isomerisiert. Das bei der katalytischen Hydrierung von 2a anfallende Gemisch der Dihydronarciclasine wird über die Tetraacetate in die cis- und trans-Verbindungen 14a und 15a aufgetrennt. Als Nebenprodukt der katalytischen Hydrierung entsteht Isonarciclasin (16a). Mit Hilfe der NMR-Spektren von 15b und 16b läßt sich die relative Konfiguration des Narciclasins entsprechend 2a beweisen. Lycoricidin und Margetin sind identisch und haben die Konfiguration 2b. Über einige biologische Teste wird berichtet.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080210
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 51
    Electronic Resource
    Electronic Resource
    Komplexchemie reaktiver organischer Verbindungen, V. Reaktionen aliphatischer Diazoverbindungen mit thermolabilen Mangan-Komplexen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 486-499 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Complex Chemistry of Reactive Organic Compounds, V. Reaction of Aliphatic Diazo Compound with Thermolabile Manganese ComplexesAliphatic diazo compounds react with the manganese- tetrahydrofurane complexes 1 and 2, respectively, to yield olefine, ketimine or carbene complexes: 3-diazo-2- butanone (3b) reacts with 2 under intramolecular hydride transfer to give the buten-2- one complex 7, while 3-diazocamphor (3c) leads to the 3-iminocamphor complex 8. Benzolyphenyldiazomethane (3a), diphenyldiazomethane (9a), and its p-substituted derivatives 9b-f are shown to be preliminary stages for the stable carbene complexes 4, 10, and 11, the spectra of which are discussed. The diphenylcarbene ligand can be split off by triphenylphosphine, carbon monoxide, ammonium cerium(IV) nitrate, and by thermolysis.
    Notes: Aliphatische Diazoverbindungen reagieren mit den Mangan-THF- Komplexen 1 bzw. 2 zu Olefin-, Ketimin- oder Carben-Komplexen: Während 3-Diazo-2-butanon (3b) mit 2 unter intramolekularer Hydridverschiebung den Buten-2- on-Komplex 7 ergibt, bildet 3-Diazo-campher (3c) bei Umsetzung mit 2 den 3-Iminocampher-Komplex 8. Benzoylphenyldiazomethan (3a) sowie Diphenyldiazomethan (9a) und seine p- substituierten Derivate 9b-f verhalten sich gegenüber 1 und 2 als Vorstufen für die stabilen Carben-Komplexe 4, 10 und 11, deren Spektren diskutiert werden. Der Diphenylcarben-Ligand in 11a kann mit Triphenylphosphin, Kohlenmonoxid und Ammoniumcer(IV)-nitrat sowie durch Thermolyse abgespalten werden.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080213
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 52
    Electronic Resource
    Electronic Resource
    Photochemische Dimerisierung von 1,4- Dialkinylbenzolen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 528-537 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photochemical Dimerisation dof 1,4-DialkynylbenzenesOn irradiation with ultraviolet light 1,4-diethynylbenzene (4a) forms blue unstable 6-ethynyl-1-(4- ethynylphenyl)azulene (5) and 6-ethynyl-2-(4-ethynylphenyl)azulene (6) besides polymers. The photolysis of 1,4-bis(phenylethynyl)benzene (4b) yields stable green 2,3-diphenyl-6-phenylethynyl-1-[4- (phenylethynyl)phenyl]azulene (9) and the isomeric naphthalene 11. Products of catalytic reduction of 5, 9, and 11 are described.
    Notes: Aus 1,4-Diäthinylbenzol (4a) entstehen bei Bestrahlung mit ultraviolettem Licht das wenig beständige, blaue 6-Äthinyl-1-(4-äthinylphenyl)azulen (5) und 6-Äthinyl-2-(4-äthinylphenyl)-azulen (6) neben polymeren Produkten. Dagegen führt die Photolyse von 1,4-Bis(phenyl-äthinyl)benzol (4b) zu dem beständigen grünen 2,3-Diphenyl-6-phenyläthinyl-1-[4-(phenyl-äthinyl)phenyl]azulen (9) und dem isomeren Naphthalin-Derivat 11. Reduktionsprodukte von 5, 9 und 11 werden beschrieben.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080218
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 53
    Electronic Resource
    Electronic Resource
    Derivate des Methylendioxybenzols, 40. Synthese des Ferrugons und des Pseudoferrugons (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 561-568 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Derivatives of Methylendioxybenzene, 40. the Synthesis of Ferrugone and PseudoferrugoneThe isoflavones ferrugone (1a) and pseudoferrugone (1a) as well as their dihydro derivatives 2a and b are prepared from the apione derivatives 5f of 6f and the chromene or chroman derivatives 4d and 3p.
    Notes: Die Isoflavone Ferrugon (1a) und Pseudoferrugon (1b) sowie die Dihydroverbindungen 2a und b werden durch Reaktion der Apionderivate5f und 6f mit den Chromen- bzw. Chroman-derivaten 4d bzw. 36p dargestellt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080221
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 54
    Electronic Resource
    Electronic Resource
    Methylendioxyhetarene, 1. Zur Darstellung von 3,4- Methylendioxythiophen-, -furan- und pyrrol- abkömmlingen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 569-575 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Methylenedioxyhetarenes, 1. On the Preparation of 3, 4- Methylenedioxythiophene-, furan- and -pyrrole DerivativesMethylenation experiments with 3, 4-dihydroxy compounds of diethyl thiophene-, furan-, 1-phenyl-, and 1- (ethoxycarbonylmethyl)-2, 5-pyrroledicarboxylate are reported. Methylenations lead only with diethyl 3, 4-dihydroxy-2, 5- thiophenedicarboxylate (1) to the 3, 4- methylenedioxythiophene derivatives 2 and 3 with formation of diethyl dithieno[3, 4-b: 3′, 4′- g]tetroxecin-1, 3, 7, 9-tetracarboxylate (4) as by- product. The furan- (5a) and pyrrole derivatives 7a and b give the tetraethyl difuro- (6) and dipyrrolo[3, 4-b: 3′, 4′-g]tetroxecin- 1, 3, 7, 9-tetracarboxylates 8a and b, respectively.
    Notes: Es wird über Methylenierungsversuche an 3,4-Dihydroxy- Verbindungen der Thiophen-Furan-, 1-Phenyl- und 1- (Äthoxycarbonylmethyl)-2,5-pyrroldicarbonsäure- diäthylester berichtet. Die Methylenierungen führen nur beim 3,4-Dihydroxy-2,5-thiophendicarbonsäure-diäthylester (1) zu den 3,4-Methylendioxythiophen-Derivaten 2 und 3, wobei als Nebenprodukt der Dithieno[3,4-b: 3′,4′-g]tetroxecin-1,3,7,0-tetracarbonsäure- tetraäthylester (4) gebildet wird. Bei dem Furan- (5a) und den Pyrrol-Derivaten 7a und b entstehen die Difuro- (6) bzw. die Dipyrrolo[3,4- b: 3′,4′-g]tetroxecin-1,3,7,9- tetracarbonsäure-tetraäthylester 8a, b.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080222
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 55
    Electronic Resource
    Electronic Resource
    Reaktionen von N, N-Dialkyl- und N, N-Diarylsulfamiden mit Chlorsulfonylisocyanat (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 618-622 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of N, N-Dialkyl- and N, N-Diarylsullfamides with Chlorosulfonyl IsocyanateChlorosulfonyl isocyanate reacts with N, N-dialkyl- or N, N-diarylsulfamides to give the so far unknown N-chlorosulfonyl-N′-(dialkyl- and -diarylsulfamoyl)ureas (3a-e), which may be hydrolysed to the corresponding N-(dialkyl- and -diarylsulfamoyl)ureas (4a-e). The pyrolysis of 3a-e leads to the formation of the known sulfamoyl chlorides.
    Notes: Durch Umsetzung von Chlorsulfonylisocyanat mit N, N-Dialkyl- oder N, N-Diarylsulfamiden erhält man die bisher unbekannten N-Chlorsulfonyl-N′-(dialkyl- und -diarylsulfamoyl)harnstoffe (3a-e), die sich zu N-(Dialkyl- und-Diarylsulfamoyl)harnstoffen (4a-e) hydrolysieren lassen. Die Pyrolyse von 3a-e liefert die bekannten Sulfamidsäurechloride.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080227
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 56
    Electronic Resource
    Electronic Resource
    Zur Photochemie des Allens (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 657-663 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Photochemistry of AlleneAcetophenone-sensitized irradiation of allene yields a complex mixture of products, from which the allene dimer 1, the trimers 2 and 3, and the ketones 4 and 5 have been isolated. This is in contrast to the reported thermal di- and trimerization of allene, which lead to products such as 1, 8-12. The planar allene triplet 13, derived by way of a nonvertical triplet-triplet energy transfer, presumably plays a key role in the photosensitized oligomerization of allene. Also, the formation of the ketone 5 is easily explained in terms of an attack of 13, through its central C-atom to the o-position of the acetophenone, to give 16, which cyclizes ultimately to yield 5. At 240°C, 5 undergoes fragmentation to the starting materials. The α,β-unsaturated ketone 4 arises through a [2 + 2]-photocycloaddition reaction of the 3(n,π*) state of acetophenone to methylacetylene via the oxetene intermediate 6, followed by ring-opening.
    Notes: Die acetophenon-sensibilisierte Belichtung von Allen liefert eine komplexe Produktmischung, aus der sich das Allendimere 1, die Trimeren 2 und 3 sowie die Ketone 4 und 5 isolieren lassen. Dieser Befund steht im Gegensatz zur beschriebenen thermischen Di- und Trimerisierung des Allens, die zu 1, 8-12 führt. Eine Schlüsselrolle bei der photosensibilisierten Allen-Oligomerisierung spielt vermutlich das durch nichtvertikale Triplett-Triplett-Energieübertragung gebildete planare Allen-Triplett 13. Auch die Entstehung des Bicyclo[4.2.0]octadien-Ketons 5 erklärt sich zwanglos durch einen Angriff von 13 mit seinem mittleren C-Atom in der o-Position des Acetophenons unter Bildung der Zwischenstufe 16, die Ringschluß zu 5 erfährt. Bei 240°C erleidet 5 Rückspaltung in die Ausgangskomponenten. Das α,β-ungesättigte Keton 4 ist dagegen Ergebnis einer [2 + 2]-Photocycloaddition des Acetophenons im 3(n,π*)-Zustand an Methylacetylen zum Oxeten 6 mit anschließender Ringöffnung.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080231
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 57
    Electronic Resource
    Electronic Resource
    Organische Schwefelverbindungen, XI. Synthese von 1,3-Oxathiol-spirofuranonen und Furanon-spirodihy-drothiopyranen aus 4-Thioxo-tetrahydrofuran-3-onen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 673-682 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Organosulfur Compound, XI. Synthesis of 13-3-Oxathiol-spirofuranones and Furanone-spirodihydrothiopyrans from 4-Thioxotetrahydrofuran-3-onesHeterocyclic, non-enolisable α-oxo-thioketones of furan-type 9 have been prepared for the first time. These highly unstable compounds undergo dimerisation and subsequent elimination of sulfur to give 1,3-oxathiol-spirofuranones 11. In competition with this process reaction with the eliminated active sulfur can occur to yield a dispiro-1,2,4-trithiolan 10a. In the presence of dimethylbutadiene the new α-oxo-thioxofurans 9 react according to the Diels-Alder principle to form the furanone-spirodihydrothiopyrans 13. The reaction mechanisms are discussed.
    Notes: Es werden erstmals heterocyclische, nicht enolisierbare α-Oxo-thioketone vom Furantyp (9) hergestellt, die außerordentlich instabil sind und unter Dimerisierung mit anschließender Schwefeleliminierung reagieren, wobei die bisher unbekannten 1,3-Oxathiol-spirofuranone 11 entstehen. In Konkurrenz hierzu kann Reaktion mit dem bei der Fragmentierung gebildeten aktiven Schwefel unter Bildung eines Dispiro-1,2,4-trithiolans (10a) eintreten. In Gegenwart von Dimethylbutadien reagieren die neuen α-Oxo-thioxo-furane 9 ausschließlich nach dem Diels-Alder-Prinzip unter Bildung der Furanon-spirodihydrothiopyrane 13. Die Reaktions-mechanismen werden diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080233
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 58
    Electronic Resource
    Electronic Resource
    Übergangsmetall-substituierte VB-Elementsysteme, V. Bis(VIA-metall)methylstibine - Darstellung, Quartärisierung und Oxidation (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 700-715 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Substituted VB Element System. Bis(VIA metal)methylstibines-Preparation, Quaternization and OxidationCH3SbBr2 reacts with the transition metal anions of Na[Fe(CO)2π-C5H5] and Na[M(CO)3π-C5H5] (M=Cr, Mo, W) to give CH3Sb[Fe(CO)2π-C5H5]2 and CH3Sb[M(CO)3π-C5H5]2 (M=Cr, Mo, W). via stepwise metalation. Starting with the primary substitution products BrCH3Sb—M(CO)3π-C5H5 (M=Mo, W) the heteronuclear species π-C5H5(CO)3Cr—Sb-(CH3)—M(CO)3π-C5H5 (M=Mo, W) and π-C5H5(CO)3Mo—Sb(CH3)—W(CO)3π-C5H5 can be obtained. Reactions with alkyl halides result in the quaternization of the Sb-atom or the cleavage of the Sb—M bond. In the first case metal substituted Sb-cations of the type [{π-C5H5(CO)3M}2Sb(CH3)R]⊕ (M=Mo, W; R=CH3, C2H5, C6H5CH2) are formed, which can also be synthesized by reaction of monometalated stibines with metal halides [{e. g. π-C5H5(CO)3Mo—Sb(CH3)2 and π-C5H5(CO)3MoBr]. Bromine adds on VB element, to yield transition metal derivatives with presumable pentacoordinated antimony ([π-C5H5(CO)3W]2SbCH3Br2). The chemical and spectroscopic properties of the new antimony transition metal complexes are reported.
    Notes: Die Umsetzung von CH3SbBr2 mit den Übergangsmetall-Anionen von Na[Fe(CO)2π-C5H5] und Na[M(CO)3π-C5H5] (M=Cr, Mo, W) führt unter stufenweiser Metallierung zur Bildung von CH3Sb[Fe(CO)2π-C5H5]2 und CH3Sb[M(CO)3π-C5H5]2 (M=Cr, Mo, W). Ausgehend von den primären Substitutionsprodukten BrCH3Sb—M(CO)3π-C5H5 (M=Mo, W) Können die heteronuclearen Spezies π-C5H5(CO)Cr—Sb(CH3)—M(CO)3π-C5H5 (M=Mo, W) und π-C5H5(CO)3Mo—Sb(CH3)—W(CO)3π-C5H5 erhalten werden. Reaktionen mit Alkylhalo-geniden verlaufen unter Quartärisierung am Sb-Atom oder Spaltung der Sb—M-Einheit. Im ersten Fall werden metallsubstituierte Sb-Kationen der Form [{π-C5H5(CO)3M}2Sb(CH3)R]⊕; (M=Mo, W; R=CH3, C2H5, C6H5CH2) gebildet, die auch aus monometalliertem Stibin und komplexem Metallhalogenid zugänglich sind [z. B. π-C5H5(CO)3MoSb(CH3)2 und π-C5H5(CO)3MoBr]. Die Einwirkung von Brom verläuft unter Addition am VB-Element und liefert Übergangsmetallderivate mit vermutlich pentakoordiniertem Antimon([π-C5H5(CO)3W]2sbCH3Br2). Die chemischen und spektroskopischen Eigenschaften der neuen Antimon-Übergangsmetallkomplexe werden beschrieben.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080236
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 59
    Electronic Resource
    Electronic Resource
    Übergangsmetall-substituierte VB-Elementsysteme, VI. Bis(VIA-metall)methylstibine als monofunktionelle Ligandsysteme in Übergangsmetallkomplexen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 716-723 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Substituted VB Element System. Bis(VIA metal)methylstibines as Monofunction Ligands in Transition Metal ComplexesThe photochemical or thermal reaction of the metal corbonyls M(CO)6 (M=Cr, Mo, W), π-C5H5Mn(CO)3, and Fe2(CO)9 with the dimetalated stibines CH3Sb-[M′(CO)3π-C5H5]2 (M′=Cr, Mo, W) proceeds with elimination of CO or Fe(CO)5, yielding the neutral single antimony-bridged trinuclear complexes (CO)5M—Sb(CH3)[M′L4]2, π-C5H5(CO)2Mn—Sb(CH3)[M′L4]2, and (CO)4Fe-Sb(CH3)[M′L4]2. The new compounds are characterized by means of spectroscopy.
    Notes: Die photochemische bzw. thermische Umsetzung der Metallcarbonyle M(CO)6 (M=Cr, Mo, W), π-C5H5Mn(CO)3 und Fe2(CO)9 mit den dimetallierten Stibinen CH3Sb-[M′(CO)3π-C5H5]2 (M′=Cr, Mo, W) liefert unter Eliminierung von CO bzw. Fe(CO)5 die neutralen, einfach antimonverbrückten Dreikernkomplexe (CO)5M—Sb(CH3)[M′L4]2, π-C5H5(CO)2Mn—Sb(CH3)[M′L4])2 und (CO)4Fe—Sb(CH3)[M′L4]2, Die neuen Verbindungen werden spektroskopisch charakterisiert.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080237
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 60
    Electronic Resource
    Electronic Resource
    Polyacetylenverbindungen, 232. Weitere Inhaltsstoffe der Gattung Dendranthema (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 735-738 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polyacetylenic Compounds, 232. Further Constituents of the Genus DendranthemaThe genus Dendranthema, also listed as a section of Chrysanthemum, is characterized by the occurrence of 6-ring-enol ether polyynes. The structure of three new compounds has been elucidated (10-12).
    Notes: Die auch als Sektion von Chrysanthemum geführte Gattung Dendranthema ist durch das Vorkommen von 6-Ring-enolätherpolyinen charakterisiert. Drei neue Verbindungen werden in ihrer Konstitution geklärt (10-12).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080304
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 61
    Electronic Resource
    Electronic Resource
    Die Ozonolyse von 3,4-cis-Diacetyl-1,2,3,4-tetramethyl-1-cyclobuten (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 749-753 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ozonolyse of 3,4-cis-Diacetyl-1,2,3,4-tetramethyl-1-cyclobuteneThe ozonolysis of the title compound 3 gives an ozonide (9) with trans-acetyl groups in high yield. Only a two step transformation of the primary ozonide to the final ozonide via a well defined intermediated (5) can explain this result.
    Notes: Die Tasache, daß die Ozonolyse der Titelsubstanz 3 in CFCl3 in hoher Ausbeute ein Ozonid (9) mit trans-ständigen Acetylgruppen liefert, bewiest, daß der Übergang vom Primärozonid zum Ozonid nicht einstufig, sondern über ein definiertes Zwischenprodukt (5) verläft.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080307
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 62
    Electronic Resource
    Electronic Resource
    Untersuchungen an Stoffwechselprodukten von Mikroorganismen, VIII. Aldgamycin F, ein neues Antibiotikum aus Streptomyces lavendulae (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 780-789 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Investigation on Metabolites of Microorganisms, VIII. Aldgamycin F, a New Antibiotic from S. lavendulaeThe new antibiotic aldgamycin F was isolated from cultures of S. lavendulae, for which we suppose structure. 7.
    Notes: Aus Kulturen von S. lavendulae wurde das neue Antibiotikum Aldgamycin F isoliert, für das wir Struktur 7 vorschlagen.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080311
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 63
    Electronic Resource
    Electronic Resource
    Die Stereochemie der Spaltung chiraler acyclischer quartärer Phosphoniumsalze zu tertiären Phosphinoxiden mit Alkalialkoholat (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 803-812 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Stereochemistry of the Alkali Alcoholate-induced Fission of Chiral Acyclic Quaternary Phosphonium Salts to Tertiary Phosphine OxidesThe stereochemical course of the sodium ethanolate-induced fission of chiral acyclic quaternary phosphonium salts 1-5 to tertiary phosphine oxides 6-10 is (with one exception) the same as that of the cleavage of these salts by sodium hydroxide. However, in most cases the stereoselectivity is remarkably lower in the alcoholate-induced fission than in the reaction with sodium hydroxide.
    Notes: Die beobachtete Brutto-Stereochemie der Spaltung chiraler acyclischer quartärer Phosphoniumsalze 1-5 zu tertiären Phosphinoxiden 6-10 mittels Natriumäthylat ist  -  mit einer Ausnahme  -  prinzipiell die gleiche wie bei der Spaltung der betreffenden Salze mit Natrium-hydroxid. Die Stereoselektivität ist dagegen bei der Spaltung mit Alkoholat meist deutlich geringer als bei der Reaktion mit Natriumhydroxid.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080313
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 64
    Electronic Resource
    Electronic Resource
    Die Primärprodukte der Carbonsäurehydrazid/Chlorphosphoran-Reaktion: 1,3,4,2λ5-Oxadiazaphospholine (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 820-830 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Primary Products of the Carbohydrazide/Chlorophosphorane Reaction:. 1,3,4,2λ5-OxadiazaphospholinePhosphorus pentachloride and other at least difunctional chlorophosphoranes react with acylhydrazines and with N-acyl-N′-phenylhydrazines to give 1,3,4,2λ5-oxadiazaphospholines 3. Pentacoordination at phosphorus is unexpected stable in these rings. The compounds are characterized by n. m. r. and mass spectrometry. They are more or less thermolabile and decompose eliminating phosphine oxide or a phosphorus oxide chloride. Electron releasing substituents at the phosphorus and electron withdrawing substituents at the nitrogen atom increase the rate of decomposition. With triethylamine the compounds 3 loose hydrogen chloride and yield the dimers 4 of 1,3,4,2λ5-oxadiazaphospholes.
    Notes: Phosphorpentachlorid und andere mindestens difunktionelle Chlorphosphorane reagieren mit Acylhydrazinen sowie N-Acyl-N′-phenylhydrazinen zu den 1,3,4,2λ5-Oxadiazaphospholinen 3 mit unerwartet stabiler Pentakoordination am Phosphor. Die Verbindungen werden NMR- und massenspektrometrisch charakterisiert. Sie sind mehr oder weniger thermolabil und zerfallen unter Abspaltung von Phosphinoxid bzw. eines Phosphoroxidchlorids. Der Einfluß der P-, C- und N-ständigen Substituenten auf die Zerfallsgeschwindigkeit wird diskutiert. Triäthylamin spaltet aus 3 Chlorwasserstoff ab; es entstehen Dimere 4 der 1,3,4,2λ5-Oxadiazaphosphole.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080315
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 65
    Electronic Resource
    Electronic Resource
    Vier Synthesewege zu (2-Pyrimidinylamino)-n-alkansäuren (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 862-874 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Four Routes for the Synthesis of (2-Pyrimidinylamino)-n-alkanoic AcidsNucleotide analogues of amino acids with variously substituted 2-pyrimidinyl side chains are available by four synthetic routes. 1) The cyclocondensation of 2-alkyl-3-aminoacroleins (4) with amino acids containing guanidino functions (5b) gives Nδ-(5-alkyl-2-pyrimidinyl)ornithine derivatives (7). 2) Cyclocondensations of 1,3-diketones of (9) with C-(guanidino)amino acids or N-(amidino)amino acids (5a-d) yield (4,6-dialkyl-2-pyrimidinylamino)-n-alkanoic acids (10). 3) (4-Alkyl-6-oxo-1,6-dihydro-2-pyrimidinylamino)-n-alkanoic acids (13) are obtained by way of cyclocondensation of ethyl acetoacetate (12) with 5a-c. 4) The nucleophilic substitution of 2-ethylthio-6-oxo-1,6-dihydropyrimidines (14, 17) by mono- and diamino acids (15) yields (5-alkyl-6-oxo-1,6-dihydro-2-pyrimidinylamino)- and (4-alkyl-6-oxo-1,6-dihydro-2-pyrimidinylamino)-n-alkanoic acids (16, 18).
    Notes: Nucleotid-analoge Aminosäuren mit verschieden substituierten 2-Pyrimidinyl-Seitenketten sind auf vier Wegen zugänglich: Die Cyclokondensation von 2-Alkyl-3-aminoacroleinen (4) mit Aminosäuren mit Guanidinofunktion (5b) führt zu Nδ-(5-Alkyl-2-pyrimidinyl)ornithin-Derivaten (7). Cyclokondensationen von 1,3-Diketonen (9) mit C-(Guanidino)aminosäuren bzw. N-(Amidino)aminosäuren (5a-d) liefern (4,6-Dialkyl-2-pyrimidinyiamino)-n-alkansäuren (10). Durch Cyclokondensationen von Acetessigester (12) mit 5a-c sind (4-Alkyl-6-oxo-1,6-dihydro-2-pyrimidinylamino)-n-alkansäuren (13) darstellbar. Aus 2-Äthylthio-6-oxo-1,6-dihydropyrimidinen (14, 17) lassen sich durch nucleophile Substitution mit Mono- und Diaminosäuren (15) (5-Alkyl-6-oxo-1,6-dihydro-2-pyrimidinylamino)- sowie (4-Alkyl-6-oxo-1,6-dihydro-2-pyrimidinylamino)-n-alkansäuren (16, 18) erhalten.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080319
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 66
    Electronic Resource
    Electronic Resource
    Photoelektronenspektren und Moleküleigenschaften, XLV. Schwefelsäure-Derivate : Alkyl-, Vinyl- und Arylsulfone, Alkylsulfoimide und Sulfurylhalogenide (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 897-913 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photoelectron Spectra and Molecular Properties, XLV. Sulfuric Acid Derivatives : Alkyl, /Vinyl, and Aryl Sulfones, S,S-Dialkylsulfoimides and Sulfuryl HalidesThe photoelectron (PE) spectra of the following sulfuric acid derivatives are discussed comparatively using qualitative MO models supported by modified CNDO calculations. The substituent effects  -  including the isoelectronic exchange S=O → S=NH and structural modifications  -  can be summarized in correlation diagrams and rationalized as perturbations of the ++ group.
    Notes: Die Photoelektronen(PE)-Spektren der folgenden Schwefelsäure-Derivate werden mit qualitativen MO-Modellen, gestützt auf modifizierte CNDO-Rechnungen, vergleichend diskutiert. Die Substituenten-Effekte - den isoelektronischen Austausch S=O → S=NH und Strukturänderungen eingeschlossen  -  lassen sich in Korrelationsdiagrammen zusammenfassen und als Störungen der -Gruppe betrachten.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080322
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 67
    Electronic Resource
    Electronic Resource
    Gekoppelte Elektrodenreaktionen, II. Benzonitril als Reaktionsmedium für anodisch erzeugte Carbeniumionen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 967-972 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Coupled Electrode Reaction, II. Benzonitrile as a Reaction Medium for Anodically Generated Carbenium IonsBy electrolysis of pivalic acid and isobutyric acid in benzonitrile/isopropyl alcohol in undivided cells N alkylated benzylamines and N,N′-diisopropyl-1,2- diphenylethylenediamine are isolated in a total yield up to 60 percent of the condensed reaction products. The reaction path is explained by anodically generated carbenium ions which react with bezonitrile forming nitrilium ions 3. These are reduced at the cathode (6, 8) or are hydrodimerized (7). The details and the formation of by-products are discussed.
    Notes: Bei der Elektrolyse von Pivalinsäure und Isobuttersäure in Benzonitril/Isopropylalkohol in ungeteilten Zellen werden in einer Gesamtausbeute bis zu 60% der kondensierten Reaktions-produkte N-alkylierte Benzylamine und N,N′-Diisopropyl-1,2-dipnhenyläthylendiamin isoliert. Der Reaktionsverlauf wird über anodisch erzeugte Carbeniumionen erklärt, die mit Benzonitril zu Nitriliumionen 3reagieren. Diese werden an der Kathode reduziert (6, 8) oder hydrodimerisiert (7). Die Einzelheiten und die Bildung von Nebenprodukten werden besprochen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080329
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 68
    Electronic Resource
    Electronic Resource
    Masthead (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975) 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080401
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 69
    Electronic Resource
    Electronic Resource
    Natürlich vorkommende Terpen-Derivate, XLIII. Neue Sesquiterpenlactone aus Athanasia-Arten (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 357-361 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Naturally Occurring Terpene Derivatives, XLIII. New Sequiterpene Lactones from Athanasia SpeciesThe investigation of four further Athanasia species shows that furansesquiterpenes of the type 1-4 are characteristic for this genus. Besides known compounds five new sesquiterpene lactones have been isolated and their structures elucidated (6, 7, 9, 10 and 13). The close biogenetic relationships of these lactones to already known sesquiterpenes are apparent.
    Notes: Die Untersuchung von vier weiteren Athanasia-Arten zeigt, daß Furansesquiterpene vom Typ 1-4 für diese Gattung charakteristisch sind. Neben bereits bekannten Verbindungen werden fünf neue Sesquiterpenlactone isoliert und in ihrer Konstitution aufgeklärt (6, 7, 9, 10 und 13). Die engen biogenetischen Beziehungen dieser Lactone zu bereits bekannten Sesquiterpenen sind offensichtlich.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080144
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 70
    Electronic Resource
    Electronic Resource
    Hydrogenolyse kleiner Kohlenstoffringe, II. Über die Hydrierung von Basketan- und Snoutanderivaten (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 337-356 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydrogenolysis of Small Cycloalkanes, II. hydrogenation Basketane- and Snoutane-Derivativescis- and both trans-dimethyl twistane-4,5-dicarboxylates (9 and 11, 13) are formed via the dihydro intermediates 4-7 by hydrogenation of cis- and trans-dimethyl basketane-9,10-dicarboxylates (1 and 3) over Pd/C under normal conditions. During the uptake of the first mole-equivalent of hydrogen all the basketane derivatives were rearranged to snoutane derivatives (22 and 24) to some extent. The second C—C bond is cleaved on that side of the basketane skeleton, which is opposite to the first hydrogenated one. cis- and trans-dimethyl snoutane-9,10-dicarboxylates (22 and 24) were hydrogenated under the same conditions but more slowly via the dihydro derivatives (25, 27 and 29, 31) to yield cis- and trans-dimethyl isotwistanedicarboxylates (33 and 35). In snoutane derivatives the second cyclopropane ring is cleaved exclusively from the same side of the molecule as the first one. This is shown by separate hydrogenations of dihydro snoutane derivatives (27, 37 and 38). Hydrogenation of basketene (21) provides a mixture containing 70-75% of twistane (17) and 25-30% of isotwistane (39). The reasons for the different ways of hydrogenation in both systems are discussed. The configurations of all dihydro intermediates and endproducts have been established.
    Notes: cis- und trans-Basketan-9,10-dicarbonsäure-dimethylester (1 und 3) werden unter Normal-bedingungen mit Pd/C in Methanol über die isomeren Dihydrozwischenstufen (4-7) zu cis- und den beiden trans-Twistan-4,5-dicarbonsäure-dimethylestern (9 und 11, 13) hydriert. Bei der Hydrogenolyse der ersten C—C-Bindung erfolgt teilweise Umlagerung zu Snoutanderivaten (22 und 24). Die Öffnung der zweiten Bindung am Basketangerüst geschieht ausschließlich an der zur ersten hydrierten Bindung gegenüberliegenden Molekülseite. cis- und trans-Snoutan-9,10-dicarbonsäure-dimethylester (22 und 24) reagieren unter den gleichen Bedingungen ebenfalls, aber langsamer, über die Zwischenstufen (25, 27 und 29, 31) zu cis- und trans-Isotwistan-dicarbonsäure-dimethylester (33 und 35). An den getrennt untersuchten Zwischenstufen 27, 37 und 38 wird gezeigt, daß im Snoutangerüst beide Cyclopropanringe ausschließlich von der gleichen Molekülseite angegriffen werden. Aus Basketen (21) erhält man bei der Hydrierung ein Gemisch von 70-75% Twistan (17) und 25-30% Isotwistan (39). Die Ursachen für den verschiedenen Hydrierungsverlauf in beiden Systemen werden erörtert, und die Konfiguration aller Zwischenstufen und Endprodukte wird aufgeklärt.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080143
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 71
    Electronic Resource
    Electronic Resource
    Die Synthese von 5α-Stigmasta-22,25-dien-3β-ol, 5α-Stigmast-22-en-3β-ol und 5α-Stigmastan-3β-ol und ihren 24-Epimeren (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1101-1110 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Synthesis of 5α-Stigmasta-22,25-dien-3β-ol, 5α-Stigmast-22-en-3β-ol und 5α-Stigmastan-3β-ol and their 24-EpimersThe synthesis of the title compounds from butynylcarbinols 5 with 1-dimethylamino-1-methoxy-1-propene in a Claisen rearrangement via the amides 7 is described. An effective preparation of the starting materials is given and the data of the products are compared with those from natural sterols.
    Notes: Die Synthese der Titelverbindungen aus den Butinylcarbinolen 5 mit 1-Dimethylamino-1-methoxy-1-propen in einer Claisen-Umlagerung über die Amide 7 wird beschrieben. Eine effektive Darstellung der Ausgangsverbindungen wird angegeben, und die Daten der Produkte werden mit den aus Naturstoffen gewonnenen verglichen.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080415
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 72
    Electronic Resource
    Electronic Resource
    Aromatische Diazoniumsalze, VI; Nitroso-acyl-amine und Diazoester, XIV Eine neue Reaktionsweise des N-Nitrosoacetanilids (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1027-1035 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Aromatic Diazonium, VI; Nitrosoacylamines and Diazoesters, XIV A New Reaction Mode of N-NitrosoacetanilideA side reaction in the decomposition on N-nitrosoacetanilide in ethanol/potassium acetate, which has been described to produce a salt K[C8H8N3O3]6), was reinvestigated. It is probale that this compound is formed by a free radical addition of NO to the nitroso group of N-nitrosoacetanilide and subsequent reduction. The potassium salt and the corresponding silver salt are considered to be derived from N-nitroso-N-(N-phenylacetamido)hydroxylamine (7) in agreement with spectroscopic data. Dynamic n. m. r. allows to measure a rotation process with ΔG≠ = 16.0 and ΔG° = 0.6 kcal/mole.
    Notes: Eine früher beschriebene6) Nebenreaktion beim Zerfall des N-Nitrosoacetanilids in Äthanol/Kaliumacetat, die zur Bildung eines Salzes K[C8H8N3O3] führte, wurde erneut untersucht. Es ist wahrscheinlich, daß diese Verbindung durch radikalische Addition von NO an die Nitrosogruppe des N-Nitrosoacetanilids und anschließende Reduktion entsteht. Das Kaliumsalz und ein entsprechendes Silbersalz werden in Übereinstimmung mit spektroskopischen Daten als Salze des N-Nitroso-N-(N-phenylacetamido)hydroxylamins (7) formuliert. Die NMR-Linienformanalyse gestattet die Messung einer Rotationsschwelle mit ΔG≠ = 16.0 und ΔG° = 0.6 kcal/ mol.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080407
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 73
    Electronic Resource
    Electronic Resource
    Reaktionen mit Derivaten aus der (CH)8CH2-Reihe; der dirigierende Einfluß von Substituenten bei der Photolyse einiger cis-3a, 7a-Dihydroindene (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1052-1073 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions with Derivatives of the (CH)8CH2-Family; the Governing Influence of Substituents on the Photolysis of Several cis3a,7a-DihydroindenesOn photochemical or thermal activation the tricyclo[4.3.0.02,5]nonadienes 10, 12, 14a, b, 16 are transformed to the cis-dihydroindenes 11, 13, 15a, b, 17. As determined by the reaction halflives at 120 and 153°C, respectively, the thermal stability of the starting compounds decreases in the order 14b 〉 14a ⋍ 16 〉 12 〉 10; steric reasons are discussed as a possible explanation for this sequence. Cycloaddition reaction of 11, 13, 15a, b, (17 is unreactive) with maleic anhydride and 4-phenyl-1,2,4-triazoline-3,5-dione, respectively, yield the adducts 21(21′)a, b, 22a, b, 24 and 25 for which the endo-configuration of the carbocyclic five-membered ring with respect to the C-8/C-9 double bond is unambigously proven at least in the case of 22a, b by formation of the cagephotoproducts 23a, b. Irradiation of the dihydroindenes involves different pathways: while excitation of 13 leads back to the tricyclic diene 12 the tetraesters 15a, b are converted to the intramolecular cyclization products 28a, b, and the diphenyl-compound 17 undergoes phenyl migration affording the di-π-methane isomer 30; all reactions proceed in a specific manner and only under direct irradiation conditions.
    Notes: Die Tricyclo[4.3.0.02,5]nonadiene 10, 12, 14a, b, 16 wandeln sich bei photochemischer oder thermischer Aktivierung in die cis-Dihydroindene 11, 13, 15a, b, 17 um. Aus den bei 120 bzw. 153°C ermittelten Halbwertszeiten der Isomerisierungen ergibt sich für die Ausgangsverbindungen eine in der Reihenfolge 14b 〉 14a ⋍ 16 〉 12 〉 10 abnehmende thermische Stabilität; als Ursache hierfür werden sterische Faktoren diskutiert. Cycloadditonen von Maleinsäureanhydrid bzw. 4-Phenyl-1.2.4-triazolin-3.5-dion an 11, 13, 15a, b (17 reagiert nicht) liefern die Addukte 21(21′)a,b, 22a,b,24 und 25 für welche die endo-Anordnung des carbocyclischen Fünfrings bezüglich der C-8/C-9-Doppelbindung zumindest für 22,a b duch die photochemische Bildung der Käfigverbindungen 23a, b, gesichert ist. Ber der Belichtung der Dihydroindene ist das Ergebnis sehr unterschiedlich: während der Diester 13 den Tricyclus 12 zurückbildet, werden die Tetraester 15a, b in einer intramolekularen Cyclisierung zu 28a, b und das Diphenyl-Substrat 17 in einer Di-π-Methan-Umlagerung zu 30 umgewandelt; alle Reaktionen verlaufen spezifisch und nur unter direkten Bestrahlungsbedingungen.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080411
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 74
    Electronic Resource
    Electronic Resource
    Neue Derivate des Fluorenon-hydrazons (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1138-1141 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New Fluorenone Hydrazone DerivativesThe triaminoguanidines 3a and b and N-[bis(methylthio)methylene]-N′-fluorenylidenehydrazine (4) have been synthesized. Compound 4 reacted with amines and hydrazine hydrate to give S-methylisothioureas (5), aminoguanidines (6), and triaminoguanidines (7), respectively.
    Notes: Es wurden die Triaminoguanidine 3a und b sowie das N-[Bis(methylthio)methylen]-N′-fluorenylidenhydrazin (4) synthetisiert. Die Reaktion von 4 mit Aminen bzw. Hydrazinhydrat führte in die Reihe der S-Methylisothioharnstoffe (5), Aminoguanidine (6) und Triaminoguanidine (7).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080420
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 75
    Electronic Resource
    Electronic Resource
    Umsetzungen N-substituierter Amidine mit Heterokumulenen, V. Umsetzungen mit Isothiocyanaten und Isocyanaten (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1142-1155 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of N-Substituted Amidines with Heterocumulenes, V. Reactions with Isothiocyanates and IsocyanatesN1, N2-Dialkyl-substituted amidines (e.g. 1) react with methyl isothiocyanate at room temperature to give thiocarbamoylamidines (e. g. 6) without an intramolecular hydrogen bond, whereas at elevated temperatures cyclic 1: 2-adducts (30-32) are formed. Aromatic isothiocyanates yield exchange products (34-37), whereas cyclic amidines (15-17) yield thiocarbamoylamidines (20, 26, 27) with intramolecular NH…N-bridges because of lower steric hindrance around R2. - The reaction between N1, N2-dialkyl-substituted amidines and isocyanates in the presence of larger groups R2 or strongly electron-withdrawing groups R5 yields only instable carbamoylamidines. The zwitter-ion intermediate (4) then undergoes an intramolecular reaction to give exchange products or adds a dipolarophile to yield 1,3,5-triazacyclohexane derivatives (46, 47, 51-54). These products are not formed when attack on C-2 is rendered considerably more difficult by R2 (tert-C4H9) (43, 56) or when R2=CH3 favours the formation of a very strong hydrogen bond (55).
    Notes: N1, N2-Dialkylsubstituierte Amidine (z. B. 1) reagieren mit Methylisothiocyanat bei Raumtemperatur zu Thiocarbamoylamidinen ohne intramolekulare Wasserstoffbrücke (z. B. 6), bei höheren Temperaturen zu cyclischen 1:2-Addukten (30-32). Aromatische Isothiocyanate führen zu Austauschprodukten (34-37), cyclische Amidine (15-17) geben dagegen Thiocarbamoylamidine (20, 26, 27) mit intramolekularen NH…N-Brücken infolge sterischer Entlastung um R2.  -  Die Umsetzung N1, N2-dialkylsubstituierter Amidine mit Isocyanaten führt in Gegenwart größerer Reste R2 oder stark elektronenabziehender Substituenten R5 nur zu instabilen Carbamoylamidinen. Das intermediär entstehende Zwitterion (4) reagiert dann intramolekular zu Austauschprodukten oder unter Anlagerung eines Dipolarophils zu 1,3,5-Triazacyclohexanderivaten (46, 47, 51-54). Diese Produkte werden nicht gebildet, wenn R2 (tert-C4H9) den Angriff an C-2 beträchtlich erschwert (43, 56) oder R2=CH3 die Ausbildung einer besonders festen Wasserstoffbrücke begünstigt (55).
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080421
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 76
    Electronic Resource
    Electronic Resource
    Lichtreaktionen mit Carbonsäurederivaten, IX. Abfangversuche mit photochemisch erzeugtem monoatomarem und diatomarem Schwefel. Schwefeladdition an 1,2-Dimethylencyclohexan. - Synthese von 1,4,5,6,7,8-Hexahydrobenzo[d][1,2]dithiin und 1,3,4,5,6,7-Hexahydrobenzo[c]thiophen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 630-639 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photoreactions with Carbonic Acid Derivatives, IX. Experiments on the Capture of Photochemically Produced Monoatomic and diatomic sulfur-Sulfur Addition on 1,2-Dimethylenecyclohexane.-Synthesis of 1,4,5,6,7,8-Hexahydrobenzo-[d][1,2]dithiin and 1,3,5,6,7-Hexahydrobenzo[c]thiopheneIn addition to cis- and trans-2,3-diethoxy-2-butene (3) small amounts of 2,3-diethoxy-1-butene (6), 2,3-diethoxy-1,3-butadiene (7) and 1-ethoxy-1-ethanethiol (5) were found in the irradiation product of O-ethyl thioacetate. The produced sulfur adds to a slight extent to 1,2-Dimethylenecyclohexane giving 1,4,5,6,7,8-hexahydrobenzo[d][1,2]dithiin (8), 1,3,4,5,6,7-hexahydrobenzo-[c]thiophene (9) and 4,5,6,7-tetrahydrobenzo[c]thiophene (10). For definite identification of the reaction products 8, 9 and 10 were synthesized.
    Notes: Im Bestrahlungsprodukt von Thionessigsäure-äthylester (1) wurden neben cis- und trans-2,3-Diäthoxy-2-buten (3) in geringen Mengen noch 2,3-Diäthoxy-1-buten (6); 2,3-Diäthoxy-1,3-butadien (7) und α-Mercaptodiäthyläther (5) nachgewiesen. - Der gebildete Schwefel addiert sich in geringem Ausmaß an 1,2-Dimethylencyclohexan unter Bildung von 1,4,5,6,7,8-Hexahydrobenzo[d][1,2]dithiin (8), 1,3,4,5,6,7-Hexahydrobenzo[c]thiophen (9) und 4,5,6,7-Tetrahydrobenzo[c]thiophen (10). Zur sicheren Identifizierung der Reaktionsprodukte wurden 8, 9 und 10 synthetisiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080229
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 77
    Electronic Resource
    Electronic Resource
    Acylgruppenwanderung, V. Kinetische Daten der Acylgruppenwanderung von 2-Benzoyl-3-indenyl-acetat und 3-Benzoyl-2-indenyl-acetat (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 683-692 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Acyl Group Migration, V. Kinetic Parameters of Acyl Group Migration in 2-Benzoyl-3-indeny Acetate and 3-Benzoyl-2-indenyl Acetate2-Acyl-1-indanones 6 and 8, obtained by ester condensation from 1-indanone, react with acetyl chloride to form the corresponding enolesters 7 and 9. In solution the Z-isomers, (Z)-2-(1-acetoxyethylidene)-1-indanone (7B) and (Z)-2-(1-acetoxybenzylidene)-1-indanone (9aB) as well as 9bB and 9cB show a rapid equilibrium by acetyl group migration with the 2-acyl-3-indenyl acetates 7C and 9C:7B ⇄ 7C, 9B ⇄ 9C. The isomerisation of the semicyclic C=C double bond 7B ⇄ 7A or 9B ⇄ 9A is catalysed photochemically. The kinetic parameters of the acetyl group migration have been determined by n. m. r. line-shape analysis for the isomeric enol esters 2-benzoyl-3-indenyl acetate (9aC) and 3-benzoyl-2-indenyl acetate (10C).
    Notes: Die durch Esterkondensation aus 1-Indanon erhaltenen 2-Acyl-1-indanone 6 und 8 werden mit Acetylchlorid in die zugehörigen Enolester 7 und 9 übergeführt. Die Z-Isomeren, (Z)-2-(1-Acetoxyäthyliden)-1-indanon (7B) und (Z)-2-(1-Acetoxybenzyliden)-1-indanon (9aB) sowie 9bB und 9cB liegen in Lösung durch schnelle Acetylgruppenwanderung im Gleich-gewicht mit den 2-Acyl-3-indenyl-acetaten 7C und 9C vor: 7B ⇄ 7C bzw. 9B ⇄ 9C. Die Isomerisierung der semicyclischen C=C-Doppelbindung 7B ⇄ 7A bzw. 9B ⇄ 9A wird photochemisch erreicht. Durch eine NMR-Linienformanalyse wurden die kinetischen Daten der Acetylgruppenwanderung am Beispiel der beiden isomeren Enolester 2-Benzoyl-3-indenylacetat (9a C) und 3-Benzoyl-2-indenyl-acetat (10 C) ermittelt.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080234
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 78
    Electronic Resource
    Electronic Resource
    Notiz über Donor-Akzeptor-komplexe zwischen Organylhalogenboranen und Diorganylchalkogenen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 724-726 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080238
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 79
    Electronic Resource
    Electronic Resource
    Abfangreaktionen kurzlebiger Radikale, XII Über die radikalische substitution am Schwefel: Induzierter Zerfall von (Thio)Carbonyldisulfiden (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1339-1345 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Short-Life Radicals, XII. Free Radical Substitution at the Sulfur Atom: The Induced Degradation of (Thio)Carbonyl DisulfidesDibenzoyl, diacetyl, bis(thiobenzoyl) disulfide (1, 2, 7), and benzoyl 4-tolyl disulfide (11) are degradated by hydrides R3SnH at 60°C about 103 times faster than in the spontaneous degradation. The products and following reactions have been established. In all cases, SH2 mechanisms are found, with attack of stannyl radicals at the (acyl bound) sulfur atom. In the case of 1, 2 and 11, ΔHspont.≠ is 35 or 34 ± 2 kcal/mole at 150°C.
    Notes: Dibenzoyl-, Diacetyl-, Bis(thiobenzoyl)disulfid (1, 2, 7) und Benzoyl(4-tolyl)disulfid (11) werden durch Hydride R3SnH bei 60°C im Verhältnis zum Spontanzerfall etwa um den Faktor 103 rascher abgebaut. Produkte und Folgereaktionen werden sichergestellt. Es liegen jeweils SH2-Mechanismen mit Angriff von Stannyl-Radikalen am (acylseitigen) Schwefel vor. Bei 1, 2 und 11 ist ΔH spont.≠ = 35 bzw. 34 ± 2 kcal/mol bei 150°C.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080439
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 80
    Electronic Resource
    Electronic Resource
    Kristall- und Molekülstruktur von Bis(triphenylphosphin)iminium-tetracarbonylpropylferrat,[{(C6H5)3P}2N] [Fe(CO)4C3H7] (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1373-1383 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal and Molecular Structure of Bis(triphenylphosphine)iminium Tetracarbonylpropyliron, [{(C6H5)3P}2 N] [Fe(Co)4C3H7]The crystal and molecular structure of the title compound has been determined by X-ray diffraction methods. The yellow salt crystallizes in the monoclinic space group C2/c with 8 molecules per cell. The structure was solved by conventional methods (agreement factor R1 = 0.07). Within the trigonal bipyramidal coordination polyhedron of the [Fe(CO)4C3H7] anion, the propyl group occupies an axial position. The bond length Fe-Cpropyl is 220(2) pm, the Fe-Cco distances are equal within experimental error (mean value 175(2) pm). The distances within the [{(C6H5)3P}2N] cation are similar to those found for the same ion in different crystalline salts. However, unexpectedly, an hitherto unknown new conformation is observed for the cation.
    Notes: Die Kristall- und Molekülstruktur der Titelverbindung wurde durch Röntgenbeugungsanalyse bestimmt. Das gelbe Salz kristallisiert in der monoklinen Raumgruppe C2/c mit 8 Molekülen in der Elementarzelle. Die Lösung der Struktur erfolgte mit konventionellen Methoden (Übereinstimmungsfaktor R1 = 0.07). Im [Fe(CO)4C3H7]-Anion besetzt die Propylgruppe eine axiale Position des trigonal-bipyramidalen Koordinationspolyeders um das Eisen. Die Fe-CPropyl-Bindungslänge beträgt 220(2) pm, die Fe-Cco-Abstände sind innerhalb der Fehlergrenzen gleich lang (Mittelwert: 175(2) pm). Die Abstände innerhalb des [{(C6H5)3P}2N]-Kations unterscheiden sich nicht von denen, die für das gleiche Ion in verschiedenen kristallinen Salzen gefunden wurden; unerwarteterweise liegt das Kation jedoch in einer neuen, bislang unbekannten Konformation vor.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080504
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 81
    Electronic Resource
    Electronic Resource
    Reaktionen mit Cyclobutendionen, XXXVII. Umsetzungen des (2,5-Dimethoxyphenyl)phenyl- und des Diphenylcyclobutendions mit Diazoalkanen. Ein Beitrag zur Isomerie der möglichen 1-Pyrazoline (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1413-1420 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions with Cyclobutenediones, XXXVII. Reactions of (2,5-Dimethoxyphenyl)phenyl-and Diphenylcyclobutenedione with Diazoalkanes. A Contribution to the Study of Isomerism of Possible 1-Pyrazolines(2,5-dimethoxyphenyl)phenylcyclobutenedione (7) reacts with diazomethane to give only 3a-(2,5-Dimethoxyphenyl)-4-methoxy-6-oxo-6a-phenyl-3,3a,6,6a-tetrahydrocyclopentapyrazole (8a). In glacial acetic acid 8a isomerizes to the 2-pyrazoline 9a. Diphenylcyclobutenedione (1) reacts with diazoethane to yield the diastereomeric 1-pyrazolines 10 and 11. These two compounds isomerize in glacial acetic acid to form the same 2-pyrazoline 12 and react with acetyl chloride to give the same N-acetyl derivative 13. In xylene 10 reacts to form the 4-ethoxy-3,6-dimethyl-1,5-diphenylbicyclo[3.1.0]hex-3-en-2-one (14), while in boiling tetrahydronaphthalene 10 gives two isomeric phenols 16 and 18.
    Notes: (2,5-Dimethoxyphenyl)phenylcyclobutendion (7) reagiert mit Diazomethan in Benzol ausschließlich zu 3a-(2,5-Dimethoxyphenyl)-4-methoxy-6-oxo-6a-phenyl-3,3a,6,6a-tetrahydrocyclopentapyrazol (8a). Dieses kann in Eisessig zum 2-Pyrazolin 9a umgelagert werden. Diphenylcyclobutendion (1) reagiert mit Diazoäthan zu zwei diastereomeren 1-Pyrazolinen 10 und 11. Beide ergeben in Eisessig das gleiche 2-Pyrazolin 12 sowie mit Acetylchlorid das N-Acetyl-Derivat 13. In Xylol wird 10 in das 4-Äthoxy-3,6-dimethyl-1,5-diphenylbicyclo[3.1.0]hex-3-en-2-on (14) und in Tetralin in die isomeren Phenole 16 und 18 übergeführt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080508
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 82
    Electronic Resource
    Electronic Resource
    Über Phosphazene, LII. Disproportionierung von PCl3 und CH3PCl2 bei der Cyclokondensation mit einem Amino-di(phosphazen) (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1454-1459 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphazenes, LII. Redox Disproportionation of PCl3 and CH3PCl2 during the condensation with an Aminodi(phosphazene)In a condensation and concomitant redox disproportionation CH3PCl2 and PCl3 convert the NPNPN chain of bis(aminodiphenylphosphorus) nitride chloride 6 into six-membered rings. 2-Chloro-2-methylcyclotri(phosphazene) 12 and spirobi[cyclotri(phosphaza)]pentaene 8 (as hydrochloride 7, X = Cl) are obtained, respectively. An intermediate of the spirophosphazene formation is the chloro-hydrido-λ5- or the λ3-phosphazene 4, X = Cl, or 5, respectively. It is of importance, that the second rings starts to form before the spiro center is oxidized. Competing oxidation by CCl4 leads to the gem. dichlorophosphazene 13, which enters no further reaction.
    Notes: Unter gleichzeitiger Redoxdisproportionierung schließen CH3PCl2 und PCl3 die NPNPN-Kette von Bis(aminodiphenylphosphor)nitridchlorid 6 zum Sechsring. Es entsteht das 2-Chlor-2-methyl-cyclotri(Phosphazen) 12 bzw. das Spirobi[cyclotri(phosphaza)]pentaen 8 (als Hydrochlorid 7, X = Cl). Zwischenstufe der Spirophosphazen-Bildung ist das Chlor-hydrido-λ5-oder das λ3-Phosphazen 4, X = Cl, bzw. 5. Wesentlich ist, daß die Angliederung des zweiten Rings noch vor der Oxidation des Spirozentrums eingeleitet wird. Die konkurrierende Oxidation mit CCl4 führt zum gem. Dichlorphosphazen 13, das nicht mehr weiterreagiert.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080513
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 83
    Electronic Resource
    Electronic Resource
    Gehinderte Ligandbewegung in Übergangsmetallkomplexen, IV. 13C-NMR-Studien an Tricarbonyl-η6-cyclopolyen-Komplexen der Elemente der VI. Nebengruppe (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1502-1510 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hindered Ligand motion in Transition Metal Complexes, IV 13C N.M.R. Studies on Tricarbonyl-η6 -cyclopolyene complexes of the VIB ElementsThe 13C n.m.r. spectra of some tricarbonyl-n6-cyclopolyene complexes of the VIB elements with the cyclopolyenes 1,3,5-cycloheptatriene, 1,3,5-cyclooctatriene, and 1,3,5,7-cyclooctatetraene are reported. Two novel ligand movements have been detected in this group of half-sandwich complexes: 1. A hindered rotation of the cyclopolyene ligands around the prolonged threefold axis of the tricarbonylmetal groups with free energies of activation from 11.3 to 12.7 ± 0.3 kcal/mole. 2. The 1,3,5-cyclooctatriene ligand in C8H10Cr(CO)3 is frozen at - 120°C into a chiral conformation. The enantiomers can be interconverted over an energy barrier of 8.3 ± 0.1 kcal/mole.
    Notes: Die 13C-NMR-Spektren einiger Tricarbonyl-η6-cyclopolyen-Komplexe der Elemente der VI. Nebengruppe mit den cyclopolyenen 1,3,5-Cycloheptatrien, 1,3,5-Cyclooctatrien und 1,3,5,7-Cyclooctatetraen werden beschrieben. Zwei neuartige Ligandbewegungen konnten an dieser Gruppe von Halbsandwichkomplexen nachgewiesen werden: 1. Eine gehinderte Rotation der Cyclopolyenliganden um die verlängerte dreizählige Achse der Tricarbonylmetallgruppen mit freien Aktivierungsenthalpien von 11.3 bis 12.7 ± 0.3 kcal/mol. 2. Der.1,3,5-Cyclooctatrienligand in C8H10Cr(CO)3 ist bei - 120°C in einer chiralen Konformation eingefroren. Die beiden Enantiomeren können über eine Energiebarriere von 8.3 ± 0.1 kcal/mol ineinander übergeführt werden.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080518
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 84
    Electronic Resource
    Electronic Resource
    Heterocyclisierungen, XV. Über die Reaktion von 2,3,3-Trimethylindoleninen und 1-Methyl-3,4-dihydroisochinolin mit Acyliso(thio)cyanaten (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1541-1547 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Heterocyclizations, XV. The Reaction of 2,3,3-Trimethylindolenines and 1-Methyl-3,4-dihydroisoquinoline with Acyliso(thio)cyanates5-Methoxy- and 5-nitro-2,3,3-trimethylindolenines (7a, b) react with dielectrophilic iso(thio)cyanates to give the pyrimido[3,4-a]indoles 14, 15. Furthermore, 7a affords a dicarbamoylmethylene derivative 16, which undergoes cyclization to the pyrimidinylidene indole 17. 1-Methyl-3,4-dihydroisoquinoline (21) condenses with dielectrophilic iso(thio)cyanates to the pyrimido[6,1-a]isoquino-lines 24, hitherto unknown in this stage of saturation.
    Notes: 5-Methoxy- und 5-Nitro-2,3,3-trimethylindolenin (7a, b) reagieren mit dielektrophilen Iso(thio)-cyanaten zu den Pyrimido[3,4-a]indolen 14, 15. Darüber hinaus bildet 7a ein Dicarbamoyl-methylenindol 16, das zum Pyrimidinylidenindol 17 cyclisiert. 1-Methyl-3,4-dihydroisochinolin (21) liefert mit dielektrophilen Iso(thio)cyanaten die in der vorliegenden Sättigungsstufe noch nicht beschriebenen Pyrimido[6,1-a]isochinoline 24.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080523
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 85
    Electronic Resource
    Electronic Resource
    Alkylierung von Polyphenolderivaten, III. 2,6-Di-n-alkyl-1,4-benzochinone mit langen Alkylketten (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1570-1579 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Alkylation of Polyphenol Derivatives, III. 2,6-Di-n-alkyl-1,4-benzoquinones with Long Alkyl ChainsThe syntheses of 1,4-benzoquinones 7, 13, and 23, substituted in the 2,6-positions with dodecyl residues, are described. The corresponding phenol ethers were acylated with dodecanoic acid/boron trifluoride and/or metalated and then alkylated with 1-bromododecane. The dialkylated phenol ethers 5, 11, and 20 were demethylated with boron tribromide and dehydrogenated to the corresponding benzoquinones with nitric acid or iron(III) sulfate, respectively.
    Notes: Es wird die Synthese der 2,6-Dodecyl-1,4-benzochinone 7, 13 und 23 beschrieben. Die Einführung der Dodecylreste erfolgte durch Acylierung entsprechender Phenoläther mit Dodecansäure/Bortrifluorid und/oder Metallierung der Phenoläther mit anschließender Alkylierung durch 1-Bromdodecan. Die dialkylierten Phenoläther 5, 11 und 20 wurden mit Bortribromid entmethyliert und mit Salpetersäure bzw. Eisen(III)-sulfat zu den Chinonen dehydriert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080526
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 86
    Electronic Resource
    Electronic Resource
    Ein einfacher Zugang zu 1-Azaspiro[5.5]undecanen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1623-1629 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A Simple Aproach to 1-Azaspiro[5.5]undecanesThe chemical behaviour and the synthesis of 1-azaspiro[5.5]undecane-2,7-diones 5 by Schmidt-reaction of alkyl 1-alkyl-2-oxo-1-cyclopentane carboxylates 3 to alkyl 2-alkyl-6-oxo-2-piperidine-carboxylates 4 and their cyclisation is described.
    Notes: Das chemische Verhalten und die Synthese der 1-Azaspiro[5.5]undecan-2,7-dione 5 durch Schmidt-Reaktion von 1-Alkyl-2-oxo-1-cyclopentancarbonsäure-alkylestern 3 zu 2-Alkyl-6-oxo-2-piperidin-carbonsäure-alkylestern 4 und deren Cyclisierung werden beschrieben.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080531
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 87
    Electronic Resource
    Electronic Resource
    1,2,3-Butatrien durch Diels-Alder-Spaltung (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1655-1658 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,2,3-Butatrien durch Diels-Alder RetrogressionThe pyrolysis of 1 leads to indane (6), whereas 2,3, and 4 yield 1,2,3-butatriene (5) by a Diels-Alder-retrogression.
    Notes: Die Pyrolyse von 1 führt zu Indan (6), während 2,3 und 4 unter Diels-Alder-Spaltung zerfallen und 1,2,3-Butatrien (5) liefern.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080534
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 88
    Electronic Resource
    Electronic Resource
    Umsetzungen von Ketonen mit azavinylogen Säureamiden (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1756-1767 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Ketones with Azavinylogue CarboxamidesKetones with a methyl or methylene group in the α-position react with monohydrazones of glyoxal in the presence of bases to give hydrazonoethylidene derivatives (16 + 12, 13 or 15 → 19 or 17). From these compounds 4-ketocarboxylic acids 22, 4-ketoaldehydes 27, pyrroles 28, 29, and N-aminopyrroles 31, 35, 37 can be prepared.
    Notes: Ketone mit α-ständiger Methyl- oder Methylengruppe reagieren mit Monohydrazonen des Glyoxals in Gegenwart von basen zu den entsprechenden Hydrazonoäthyliden-Derivaten (16 + 12. 13 oder 15 → 19 bzw. 17). aus diesen Verbindungen lassen sich durch Hydrolyse bzw. Reduktion 4-Ketocarbonsäuren 22, 4-Ketoaldehyde 27, Pyrrole 28, 29 oder N-Aminopyrrole 31, 35, 37 darstellen.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080542
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 89
    Electronic Resource
    Electronic Resource
    Über die Reaktion von Diphosphanen mit Tetrachlorkohlenstoff (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1783-1790 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Reaction of Diphosphanes with Carbon TetrachlorideTetraphenyl- and tetracyclohexyldiphosphane as well as the long chain tetraalkyldiphosphanes are easily cleaved by CCl4 leading to the chlorophosphines R2PCl (2a-d) and (trichloromethyl)- phosphines R2PCCl3 (3a-d). The diphosphane monoxide 4 and the diphosphacyclohexane 7 decompose in the same manner. The reaction is reversible at temperatures above 100°C. Tetramethyl- and tetraethyldiphosphane react in substance or in unpolar solvents to form the diphosphanium(1+) chlorides 9e and 10f; the careful hydrolysis of the latter gives the (chloromethyl)-diphosphanium(1+) chlorides 11 e and f.
    Notes: Tetraphenyl- und Tetracyclohexyldiphosphan sowie die längerkettigen Tetraalkyldiphosphane werden durch CCl4 glatt zu den Chlorphosphinen R2PCl (2a-d) und(Trichlormethy1)phosphinen( R2PCCl3 3a-d) gespalten. In gleicher Weise wird auch das Diphosphanmonoxid 4 sowie das Diphosphacyclohexan 7 abgebaut. Die Reaktion ist bei Temperaturen über 100°C reversibel. Tetramethyl- und Tetraäthyldiphosphan reagieren in Substanz oder unpolaren Lösungsmitteln zu den Diphosphanium(1 +)-chloriden 9e und 10f. Die vorsichtige Hydrolyse von 9e und 10f führt zu den (Chlormethyl)diphosphanium(1 +)-chloriden 11e und f.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080602
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 90
    Electronic Resource
    Electronic Resource
    Stereochemie aliphatischer Carbokationen, 9. Substituenteneffekte bei der 1,2-Wasserstoffverschiebung (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1839-1854 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Stereochemistry of Aliphatic Carbocations, 9. Substituent Effects in 1,2 Hydride ShiftsThe sterochemistry at the origin of 1,2 hydride shifts has been studied with 2-methylbutylamines which were substituted at the 2-methyl site by isopropyl (10), isopropenyl (26), phenyl (32) and methoxy groups (50), respectively. The deamination of these amines afforded tertiary alcohols (3) as the major products. Predominant retention of configuration at the chiral center was observed which increased from 7 to 27% in the order of substituents given above. The results may be attributed to partial delocalization of the incipient positive charge by π- and n-donors.
    Notes: Die Stereochemie am Ausgangspunkt von 1,2-Wasserstoffverschiebungen wurde an 2-Methylbutylaminen untersucht, deren 2-Methylgruppe Isopropyl-(10), Isopropenyl-(26), Phenyl-(32) oder Methoxy-Substituenten (50) trug. Die Desaminierung dieser Amine lieferte tertiäre Alkohole (3) als Hauptprodukte. Wir beobachteten überwiegende Konfigurationserhaltung am chiralen Zentrum, die in der oben angegebenen Reihenfolge der Substituenten von 7 auf 27% zunahm. Dieses Ergebnis kann mit einer partiellen Delokalisierung der entstehenden positiven Ladung durch π- und n-Donatoren erklärt werden.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080608
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 91
    Electronic Resource
    Electronic Resource
    Torfmoosmembranochrome, 2. Die Struktur des Sphagnorubins (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1166-1181 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cell Wall Pigments of Peat Mosses, 2. The Structure of SphagnorubinThe structure of the red cell wall pigment sphagnorubin has been elucidated. It is the anhydro-base of an anthocyanidin with a 2-phenylphenanthro[2,1-b]pyran skeleton which is hitherto unknown for flavonoids.
    Notes: Die Struktur des roten Torfmoosmembranochroms Sphagnorubin wurde aufgeklärt. Es ist die Anhydrobase eines Anthocyanidins mit einem für Flavonoide bislang unbekannten 2-Phenyl-phenanthro[2,1-b]pyran-Ringgerüst.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080423
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 92
    Electronic Resource
    Electronic Resource
    Die Ozonisierung von Alkyliden- und Benzylidenadamantanen (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1198-1206 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Ozonolysis of Alkyliden- and BenzylidenadamantanesFrom the adamantane derivatives 4-7 normal ozonides could be obtained by treatment with ozone in pentane. The olefines 9 and 10 do not react with ozon. Methanol and tetracyanoethylene respectively interfere in the known manner. 4 and 8 form primary ozonides, which are stable at -78°C.
    Notes: Die Adamantanderivate 4-7 geben bei der Ozonbehandlung in Pentan normale Ozonide, während die stark sterisch gehinderten Olefine 9 und 10 nicht mit Ozon reagieren. Sowohl Methanol wie Tetracyanäthylen greifen in bekannter Weise in die Ozonolyse ein. Nur bei der Ozonisierung von 4 und 8 konnten bei -78°C Primärozonide nachgewiesen werden.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080426
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 93
    Electronic Resource
    Electronic Resource
    Phosphorhaltige Kohlenhydrate, X. Reaktion von Carbonylzuckern mit Lithio-methanphosphon-säureestern. Darstellung von 1-Desoxy-D-fructose-1-phosphonsäure-dimethylester (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1229-1238 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphorus-containing Carbohydrates, X. Reaction of Carbonyl Sugars with Lithio Methanephosphonic Esters. Preparation of Dimethyl 1-deoxy-D-fructose-1-PhosphonateLithio-methyl-methanephosphonate (5) reacts with 2,3:4,5-di-O-isopropylidene-D-arabinose (4) to form gluco-and manno-compounds 6 + 8 which can be oxidized to the 1-deoxy-D-fructose-1-phosphonate derivative 10. Substituted uloses react with 5 to give phosphonomethyl branched sugars. 3-ulose 11 yields the allo-compound 12, hydrolysis of which leads to the aldehyde 14 which in turn yields an oxaphosphorinane 16 after reduction with sodium borohydride and ester exchange. Uloses 17 and 21 can be transformed to branched sugar phosphonates with ribo configuration.
    Notes: Lithio-methanphosphonsäure-methylester (5) reagiert mit 2,3:4,5-Di-O-isopropyliden-D-arabinose (4) zur gluco-und manno-Verbindung 6 + 8, die mit Rutheniumtetroxid zum 1-Desoxy-D-fructose-1-phosphonsäure-Derivat 10 oxidiert werden können. Blockierte Ulosen reagieren mit 5 zu phosphonomethyl-verzweigten Zuckern. Die 3-Ulose 11 ergibt eine allo-Verbindung 12, die nach Hydrolyse zum Aldehyd 14 gespalten werden kann, der nach Reduktion mit Natriumborhydrid durch Umesterung. ein Oxaphosphorinan 16 liefert. Die Ulosen 17 und 21 lassen sich in verzweigte Zuckerphosphonate der ribo-Konfiguration überführen.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080430
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 94
    Electronic Resource
    Electronic Resource
    Sterischer Verlauf des thermischen und photochemischen Zerfalls bicyclischer Vinyl-1-pyrazoline (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1271-1284 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Stereochemistry of the Thermal and Photochemical Decomposition of Bicyclic Vinyl-1-pyrazolinesThe 1,3-dipolar cycloaddition of diazomethane, diazoethane, and 3-diazo-1-propene to cyclic olefines results in the formation of the bicyclic 1-pyrazolines 8, 11-18, which form upon thermal and photochemical decomposition the hydrocarbons 9, 10, 19-32. The thermal decomposition reactions form mainly products which show inversion of configuration in reference to the starting pyrazolines, whereas the photochemical decompositions result predominantly in products where the stereochemistry of the starting materials is retained. The possibly occurring intermediates are discussed. The properties and further reactions of the resulting products are described.
    Notes: Durch 1,3-dipolare Cycloaddition von Diazomethan, Diazoäthan und 3-Diazo-1-propen an Cyclene entstehen die bicyclischen 1-Pyrazoline 8, 11-18, deren thermischer und photochemischer Zerfall die bicyclischen Kohlenwasserstoffe 9, 10, 19-32 liefert. Die entstandenen Produkte zeigen bei der thermischen Reaktion gegenüber den Ausgangsverbindungen Inversion der Konfiguration, während die Photoreaktion zu Produkten mit überwiegender Retention führt. Die bei den Reaktionen möglicherweise auftretenden Zwischenstufen werden diskutiert und die Folgereaktionen der Zersetzungsprodukte beschrieben.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080434
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 95
    Electronic Resource
    Electronic Resource
    Oxidative Kupplung von N-Methyl-Säureamiden über Kupfer-Komplexe, I. Synthese eines Piperazins aus Dimethylformamid und Kupfer(I)-cyanid (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 991-996 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Oxidative Coupling of N-Methylcarboxamides via Copper Complex Forming, I. Synthesis of a Piperazine with Dimethylformamide and Cuprous CyanideDry dimethylformamide reacts with cuprous cyanide in the presence of acetyl chloride and aerial oxygen to give 1,4-dimethyl-2,2,3,3-piperazinetetracarbonitrile (1). In 1 the 4 nitrile groups in C-2 and C-3 react, each group with a vicinal one, with methanolic ammonia to yield 2′,5′-diiminopyrrolidine rings (2). The saponfication reaction of 1 with sodium ethoxide solution with formation of 3 is described.
    Notes: Wasserfreies Dimethylformamid reagiert mit Kupfer(I)-cyanid in Gegenwart von Acetylchlorid und Luftsauerstoff zum 1,4-Dimethyl-2,2,3,3-piperazintetracarbonitril (1). In 1 reagieren je 2 vicinale Nitrilgruppen an C-2 und C-3 mit methanolischem Ammoniak zu 2′,5′-Diiminopyrrolidiniringen (2). Die Verseifung von 1 mit Natriumäthylat zu 3 wird beschrieben.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080402
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 96
    Electronic Resource
    Electronic Resource
    Zur Konjugation in makrocyclischen Bindungssystemen, XXI. Kristall- und Molekularstruktur der Käfigverbindung 2,3;6,7;10,11-Tribenzotetracyclo[6.4.0.04,12.05,9]dodeca-2,6,10-trien (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1017-1026 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Conjugation in Macrocyclic Systems, XXI. The Crystal and Molecular Structure of the Cage Compounds 2,3;6,7;10,11-Tribenzotetracyclo[6.4.0.04,12.05,9]dodeca-2,6,10-trienThe crystal structure of the title compound has been solved by direct methods and has been refined to R = 0.05. The cage compound contains the structure elements of bicyclo[2.2.2]octene, 1,5-cyclooctadiene, and cyclopentene. These subunits show deformations and sterical strain because they are forced into a cage system. Therefore long Csp3—Csp3 bond distances of 1.570 and 1.592 Å have been found. The corresponding bond angles are deformed up to 97.1°.
    Notes: Die Kristallstruktur der Titelverbindung wurde mit direkten Methoden gelöst und bis zu einem R-Wert von 0.05 verfeinert. In der Käfigverbindung sind die Strukturelemente von Bicyclo[2.2.2]-octen, 1,5-Cyclooctadien und Cyclopenten enthalten, die im Vergleich zum freien Zustand durch die Verklammerung mit Benzolkernen deformiert und sterisch gespannt sind. Daher treten besonders lange Csp3-Csp3-Bindungsabstände mit Werten von 1.570 und 1.592 Å auf. Die zugehörigen Bindungswinkel sind bis zu 97.1° deformiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080406
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 97
    Electronic Resource
    Electronic Resource
    Lupinen-Alkaloide, XLI. 13C-NMR-Spektren von Lupinen-Alkaloiden (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1043-1051 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Lupin-Alkaloids, XLI. 13C-N.M.R.-Spectra of Lupin-AlkaloidsThe analysis of the 13C-n.m.r.spectra of 47 quinolizidines and piperidines as well as some deuterated derivatives give the possibility to coordinate the found signals of the spectra of several lupin-alkaloids. The observed chemical shifts follow in general the common rules. However several particular effects can be recognized mainly due to special steric situations. The usefullness of 13C-n.m.r. spectroscopy for lupin-alkaloids has been shown.
    Notes: Die Analyse der 3C-NMR-Spektren von 47 Chinolizidinen und Piperidinen sowie einiger deuterierter Derivate gibt die Möglichkeit, die gefundenen Signale der Spektren mehrerer Lupinen-Alkaloide zuzuordnen. Die beobachteten chemischen Verschiebungen folgen im allgemeinen den übliche Regeln. Jedoch werden besondere Effekte beobachtet, die vor allem auf spezielle sterische Situationen zurückzuführen sind. Die Brauchbarkeit der 13C-NMR-Spektroskopie für Lupinen-Alkaloide wird gezeigt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080410
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 98
    Electronic Resource
    Electronic Resource
    16,17-Dihydroxy-9(11)-Kauren-18-säure - ein Bestandteil des Röstkaffees (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1093-1100 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 16,17-Dihydroxy-9(11)-Kauren-18-oic acid  - a Compound of Roasted CoffeeAtractyligenin (1) is a compound isolated from roasted coffee beans (Coffea arabica)1). 1 kg of roasted coffee contains further C19- and C20- acids up to 20 mg of each compound. It is very difficult to separate and purify these acids. One of these acids was identified as 16,17-dihydroxy-9(11)-kauren-18-oic acid (2). Its structure was confirmed by partial synthesis starting from 9(11), 16-kauradien-18-oic acid (5)2).
    Notes: Das im Röstkaffee (geröstete Bohnen von Coffea arabica) enthaltene Atractyligenin (1)1) wird von Säuren mit 19 und 20 Kohlenstoffatomen begleitet. 1 kg Röstkaffee enthält maximal bis zu 20 mg von jeder Säure, die sich dünnschichtchromatographisch nur sehr schwer trennen und reinigen lassen. Die Struktur einer dieser Verbindungen wurde als 16,17-Dihydroxy-9(11)-kauren-18-säure (2) bestimmt und durch Partialsynthese aus der 9(11),16-Kauradien-18-säure (5)2) abgesichert.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080414
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 99
    Electronic Resource
    Electronic Resource
    Synthese optisch aktiver α-Aminosäuren mit 8-Azapurinyl-Seitenkette (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1111-1117 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of Optically Active α-Amino Acids Substituted in the Side Chain with an 8-Azapurinyl Residue4-Amino-6-chloro-5-nitropyrimidine (1) or 4-chloro-5-nitro-6-oxo-1,6-dihydropyrimidine (4) react with Nα-benzyloxycarbonyl-L-lysine (2a) or 6-aminohexanoic acid (2b) to give 6-(4-pyrimidinyl-amino)hexanoic acids (3a, b, 5a, b). Reduction of their nitro group and subsequent cyclization with sodium nitrite in acidic medium yields the corresponding (triazolo[4,5-d]pyrimidine-3-yl)hexanoic acid derivatives (7a, b, 9a, b). The amino acid derivatives 7a and 9a are hydrogenated to optically active 8-azapurinyl substituted α-amino acids (10, 11).
    Notes: Durch Umsetzung von 4-Amino-6-chlor-5-nitropyrimidin (1) bzw. 4-Chlor-5-nitro-6-oxo-1,6-dihydropyrimidin (4) mit Nα-Benzyloxycarbonyl-L-lysin (2a) bzw. 6-Aminohexansäure (2b) lassen sich 6-(5-Nitro-4-pyrimidinylamino)hexansäuren (3a, b, 5a, b) darstellen. Nach Reduktion der Nitrogruppe mit Natriumdithionit werden diese mit Natriumnitrit in essigsaurem Medium zu (Triazolo[4,5-d]pyrimidin-3-yl)hexansäure-Derivaten (7a, b, 9a, b) cyclisiert. Die Aminosäure-derivate 7a und 9a können zu optisch aktiven, 8-azapurinyl-substituierten α-Aminosäuren (10, 11) hydriert werden.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080416
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 100
    Electronic Resource
    Electronic Resource
    Zum Mechanismus der Friedel-Crafts-Alkylierung mit Allylalkohol (1975)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1182-1187 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Mechanism of Friedel-Crafts Alkylation with Allyl AlcoholThe reaction between benzene and allyl alcohol in the presence of AlCl3 leads via 2-phenyl-1-propanol to 1,1-and1,2-diphenylpropane. The mechanism is investigated with the aid of deuteriated materials.
    Notes: Die Umsetzung von Benzol mit Allylalkohol in Gegenwart von AlCl3 führt über die Stufe des 2-Phenyl-1-propanols zu 1,1- und 1,2-Diphenylpropan. Der Reaktionsablauf wird vor allem mit Hilfe deuterierter Vorstufen untersucht.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19751080424
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...