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  • Organic Chemistry  (5,482)
  • Inorganic Chemistry  (5,133)
  • 42.75
  • 2005-2009  (14)
  • 2000-2004  (19)
  • 1980-1984  (6,912)
  • 1950-1954  (3,703)
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  • 1
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (0024-0672) vol.80 (2006) nr.4 p.81
    Publication Date: 2010-12-12
    Description: The new genus Lianus of subfamily Doryctinae (Hymenoptera: Braconidae) is described and illustrated. The differences from other genera of Doryctinae are discussed. Both included species originate from the Atlantic forest at Campos do Jordão, São Paulo State, Brazil.
    Keywords: Braconidae ; Doryctinae ; Lianus ; new genus ; Brazil ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 2
    Publication Date: 2007-01-16
    Description: The Pterophoridae (Ochyroticinae, Deuterocopinae, Pterophorinae (Tribus: Platyptiliini, Exelastini, Oxyptilini)) species of the Neotropical fauna are reviewed. The species are redescribed. Moths are illustrated in colour for the first time, their genitalia are illustrated in line drawings. The examination of type specimens revealed the presence of four new synonyms: Platyptilia juanvinas Gielis, 1999, is a junior synonym of Platyptilia gravior Meyrick, 1932; Platyptilia jonesi Gielis, 1996, is a junior synonym of Platyptilia semnopis Meyrick, 1931; Oxyptilus maleficus Meyrick, 1926, is a junior synonym of Leptodeuterocopus neales (Walsingham, 1915); Lioptilus parvus Walsingham, 1880, is a junior synonym of Lioptilodes albistriolatus (Zeller, 1871). During the study of much new material 40 new species were discovered: Leptodeuterocopus tungurahue, L. angulatus, L. panamaensis, L. duchicela, Sochchora mulinus, Melanoptilia nigra, Platyptilia spicula, Stenoptilodes maculatus, S. agricultura, S. heppneri, S. medius, S. altiaustralis, Postplatyptilia nebuloarbustum, P. antillae, P. caribica, P. uruguayensis, P. pluvia, P. seitetazas, P. transversus, P. carchi, P. boletus, P, ugartei, P. drechseli, P. corticis, P. zongoensis, P. vorbecki, Amblyptilia landryi, A. kosteri, Lioptilodes altivolans, L. arequipa, L. yungas, L. salarius, L. cocodrilo, Michaelophorus margaritae, M. bahiaensis, Geina integumentum, Capperia browni, Buckleria brasilia, Megalorhipida paraiso, M. dubiosa. In the larger genera the species are arranged in groups. For a distinct group of species a new genus: Melanoptilia is proposed. A comprehensive checklist of the species has been made. To facilitate identification a key is presented to the genus level.
    Keywords: Pterophoridae ; revision ; Neotropics ; new genus ; new species ; new synonyms ; new combinations ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 3
    facet.materialart.
    Unknown
    In:  NNM Technical Bulletin (13870211) vol.8 (2006) p.1
    Publication Date: 2007-01-12
    Description: A bibliography of the family Braconidae/Hymenoptera: Ichneumonidae is given for the period 1964-2003. It is an addition to Shenefelt's bibliography (1965), which covers the period 1785-1963. In total 10,436 references are listed.
    Keywords: Insecta ; Hymenoptera ; Braconidae ; bibliography ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 4
    Publication Date: 2010-12-12
    Description: The European species of the genus Helorus Latreille, 1802, are keyed and illustrated, with special reference to their distribution in The Netherlands. Three of the four European species are newly reported for The Netherlands. The description of a new species from Sulawesi (Indonesia) is added: H. celebensis spec. nov.
    Keywords: Hymenoptera ; Proctotrupoidea ; Heloridae ; Helorus, Europe ; Netherlands ; Wallacean ; Indonesia ; Sulawesi ; new species. ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 5
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (0024-0672) vol.80 (2006) nr.1 p.73
    Publication Date: 2010-12-12
    Description: Two new genera of Entedoninae are described from Afrotropical region. The genus Janicharis gen. nov. (type species: J. africana spec. nov.) is described from Cameroon, Nigeria and Madagascar. The genus Hakuna gen. nov. (type species: H. matata spec. nov.) is described from Uganda. Both genera have a rather characteristic habitus and a peculiar propodeum bearing large anterolateral strips. A new, but yet unnamed, species of the genus Trisecodes Delvare & LaSalle, 2000, is recorded from Cameroon. This is the fi rst Afrotropical record of this genus, originally described from the Neotropical region.
    Keywords: Hymenoptera ; Eulophidae ; Entedoninae ; Afrotropical region ; propodeum ; new genera ; new species ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 6
    Publication Date: 2007-01-16
    Description: In total 32 new species of Tenthredinidae are described from Vietnam and 18 new species from Indonesia: Nesoselandria albotonkinensis spec. nov., N. albeotegularissima spec. nov., N. devriesiana spec. nov., Anapeptamena achterbergiana spec. nov., Neostromboceros nigrogiganteus spec. nov., N. gracilioides spec. nov., N. alboclypeatus spec. nov., N. daoensis spec. nov., N. phuongensis spec. nov., Abusarbidea bicoloristigmata spec. nov., Eusunoxa alboapicalis spec. nov., Neopoppia tonkinometallica spec. nov., Abeleses vietnamensis spec. nov., A. metallotonkinensis spec. nov., Heptamelus tonkinensis spec. nov., Athlophorus devriesi spec. nov., Rhopographus vietnamensis spec. nov., Xenapatidea hematothoracica spec. nov., X. devriesi spec. nov., Allantidea achterbergiana spec. nov., Neothrinax nigrotonkinensis spec. nov., Indotaxonus flavissimus spec. nov., Darjilingia vietnamensis spec. nov., D. tonkinensis spec. nov., D. hoangliensis spec. nov., Ferna achterbergi spec. nov., Monophadnus bicoloritonkinensis spec. nov., Eutomostethus phongdiensis spec. nov., Eutomostethus albotegularissimus spec. nov., Tenthredo octomaculatus spec. nov., T. tricoloritonkinensis spec. nov. and T. danangiensis spec. nov. from Vietnam. Neostromboceros pleuronotatus spec. nov., N. albopedissimus spec. nov., N. flavopedis spec. nov., N. rubroguinealis spec. nov., N. rubromalayensis spec. nov., Eusunoxa malaya spec. nov., Emphytus danumiensis spec. nov., Hemibeleses sulawesiensis spec. nov., Neopoppia irregulata spec. nov., Tenthredo nigrosabahensis spec. nov., T. djampangensis spec. nov., Neothrinax kaindiensis spec. nov., N. excavata spec. nov., N. gedehensis spec. nov., Abeleses metallojavanus spec. nov., Caliroa nigrojavana spec. nov., Nesoselandria sulawesiensis spec. nov. and Athlophorus achterbergianus spec. nov. from Indonesia. Monophadnus glaucus Enderlein, 1919; Monophadnus sumatranus Enderlein, 1919; Amonophadnus nigripennis Benson, 1935; Amonophadnus nigrojavanus Haris, 2002; Corporaalinus azureus Forsius, 1925; Corporaalinus cyanescens Forsius, 1925; and Corporaalinus jacobsoni Forsius, 1929, are proposed as new synonyms of Monophadnus rivalis Konow, 1906. An identification key is added for the known Tenthredinidae of Borneo, Sumatra, Java, Sulawesi and New Guinea.
    Keywords: Hymenoptera ; Symphyta ; Tenthredinidae ; Vietnam ; Indonesia ; Malaysia ; Java ; Sumatra ; Borneo ; Celebes ; Papua New Guinea ; new species ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
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  • 7
    Publication Date: 2010-12-12
    Description: Two new host records for Exasticolus fuscicornis (Cameron, 1887)(Hymenoptera: Braconidae: Homolobinae)are presented with detailed larvae morphology and other biological information.
    Keywords: Braconidae ; Homolobinae ; Exasticolus fuscicornis ; host record ; Geometridae ; Noctuidae. ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 8
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (0024-0672) vol.80 (2006) nr.1 p.13
    Publication Date: 2010-12-12
    Description: Thirty species belonging to 16 genera of the family Braconidae (Hymenoptera) are reported from Greenland. Seven are new species described and illustrated below: Dacnusa groenlandica spec. nov.; Aphidius tarsalis spec. nov.; Praon brevistigma spec. nov.; Blacus (B.) groenlandicus spec. nov.; Cotesia crassifemorata spec. nov.; C. fascifemorata spec. nov. and Microplitis lugubroides spec. nov.
    Keywords: Braconidae ; Alysiinae ; Aphidiinae ; Blacinae ; Doryctinae ; Euphorinae ; Hormiinae ; Microgastrinae ; Rogadinae ; Nearctic ; Palaearctic ; Greenland ; distribution ; new species ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 9
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (0024-0672) vol.80 (2006) nr.4 p.91
    Publication Date: 2010-12-12
    Description: The little-known monotypic genus Paracyphocrania Redtenbacher, 1908 (Phasmatinae: Phasmatini) is reviewed and now comprises two species: P. lativentris Redtenbacher, 1908, and P. tecticollis (Redtenbacher, 1908) comb. nov., which are redescribed and illustrated. A neotype is designated for P. lativentris which is newly recorded from Sulawesi.
    Keywords: Phasmatodea ; Phasmatinae ; Phasmatini ; Paracyphocrania ; Paracyphocrania lativentris ; Vasilissa tecticollis ; Sulawesi ; Philippines ; description ; egg. ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 10
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (0024-0672) vol.80 (2006) nr.4 p.87
    Publication Date: 2010-12-12
    Description: Vestalaria vinnula spec.nov. (holotype male, southern Vietnam, Lam Dong province, Blao, 1962) is described in both sexes and compared with other species of Vestalaria May, 1935 (= the Vestalis smaragdina - group), which is ranked as valid genus.
    Keywords: Odonata ; Calopterygidae ; Vestalaria ; new species ; Vietnam ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 11
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.79-2 (2005) p.179
    Publication Date: 2007-01-16
    Description: A new species of the genus Artocella van Achterberg is described from Spain. On the basis of its substantial sexual dimorphisim, the differences between the two previously known species of this Turanian-Mediterranean genus, which had each been described from specimens of only one (and differing) sex, are reassessed.
    Keywords: Hymenoptera ; Braconidae ; Rogadinae ; Artocella ; new species ; Spain ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 12
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.79-2 (2005) p.123
    Publication Date: 2007-01-16
    Description: Dasypoda intermedia spec. nov. from Iran is described. Its description fills a gap of our knowledge of the East Mediterranean fauna of the genus Dasypoda. The West Mediterranean Dasypoda species are well known but the eastern species lack convincing records. Moreover, D. intermedia spec. nov. is a very interesting species from a phylogenetic point of view. It shares some characters common to subgenera Dasypoda s. str. and Megadasypoda Michez, 2004, which provide further evidence for the close relationship of both subgenera.
    Keywords: Hymenoptera ; Melittidae ; Dasypoda ; new species ; Iran ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 13
    Publication Date: 2007-01-16
    Description: Thirty-one species of the family Platystictidae of the Philippines are revised, i.e. all species recognised, excluding the species of the Drepanosticta halterata-group. The following new taxa are described: 16 species in Drepanosticta Laidlaw: D. acuta spec. nov., D. aurita spec. nov., D. centrosaurus spec. nov., D. clados spec. nov., D. flavomaculata spec. nov., D. furcata spec. nov., D. hermes spec. nov., D. krios spec. nov., D. luzonica spec. nov., D. malleus spec. nov., D. myzouris spec. nov., D. paruatia spec. nov., D. pistor spec. nov., D. quadricornu spec. nov., D. rhamphis spec. nov., D. trachelocele spec. nov., two in Protosticta Selys, viz. P. lepteca spec. nov. and P. plicata spec. nov., and three in Sulcosticta gen. nov., viz. S. striata spec. nov., S. pallida spec. nov. and S. viticula spec. nov. The status of eleven previously described nominal taxa is established. One, D. septima Needham & Gyger, is doubtfully considered a synonym of D. mylitta Cowley. Based on a preliminary phylogenetic analysis, the species of Drepanosticta are divided into informal species groups. Most species of the Philippines have affinities to species of Sulawesi, the Moluccas and New Guinea. Several species confined to Palawan have sister-group relationships with species from Borneo. The affinities of various other species confined to the Sulu archipelago, are unsettled as yet. The species of Platystictidae here assigned to Protosticta Selys are presumably not closely related to the type species, P. simplicinervis Selys from Sulawesi. However, a better placement has to await a more detailed phylogenetic study of the family. For three species the new genus Sulcosticta gen. nov. is erected. These species are closely allied based on the structure of the appendages, but should have been assigned to different genera if based on the present generic definitions. Many species here described have small distributional ranges, a common phenomenon in Platystictidae. Since most forests in the Philippines are heavily under threat or have already disappeared in the last fifty years, several taxa described in this paper should be considered under threat of immediate extinction.
    Keywords: Odonata ; Platystictidae ; Drepanosticta ; Protosticta ; Sulcosticta ; Philippines ; new species ; new genus ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 14
    Publication Date: 2007-01-16
    Description: In this part the remaining 78 species of the genus Pepsis, belonging to ten species-groups, are described and figured, and their phylogenetics and biogeography are discussed. 14 of the species are described as new: P. achterbergi spec. nov., P. adonta spec. nov., P. boharti spec. nov., P. caliente spec. nov., P. dayi spec. nov., P. esmeralda spec. nov., P. ianthoides spec. nov., P. jamaicensis spec. nov., P. krombeini spec. nov., P. martini spec. nov., P. multichroma spec. nov., P. nanoides spec. nov., P. wahisi spec. nov., and P. willinki spec. nov. Three species-names, P. infuscata Spinola, 1841, P. lampas Lucas, 1895, and P. thoreyi Dahlbom, 1845, are recalled from synonymy. The following 293 names are newly synonymized (the valid names are listed first): P. atalanta Mocsáry, 1885 = P. nitens Mocsáry, 1894, P. mocsaryi Lucas, 1895; P. inclyta Lepeletier, 1845 = P. mutabilis Lepeletier, 1845, P. vagabunda Lepeletier, 1845, P. cupripennis Taschenberg, 1869, P. violaceipennis Mocsáry, 1885, P. clotho Mocsáry, 1888, P. spengeli Mocsáry, 1888, P. sickmanni Mocsáry, 1888, P. nireus Mocsáry, 1894, P. atrovirens Lucas, 1895, P. cerastes Lucas, 1895, P. pygidialis Brèthes, 1908, P. guaranitica Brèthes, 1908, P. parca Lucas, 1919, P. atahualpa Banks, 1946, opimicornis, Haupt, 1952, atropos, Haupt, 1952, azurea Haupt, 1952; crassicornis Mocsáry, 1885 = P. sappho Brèthes, 1908, P. nitocris Brèthes, 1908, P. vivida Brèthes, 1908, P. arechavaletai Brèthes, 1908, P. lynchii Brèthes, 1908, P. operosa Brèthes, 1908, P. ataraqua Banks, 1946, P. splendida Haupt, 1952; P. sommeri Dahlbom, 1845 = P. azteca Cameron, 1893; P. xanthocera Dahlbom, 1843 = P. nigrescens Smith, 1855, P. fulgidipennis Mocsáry, 1885, P. juno Brèthes, 1908, P. ismare Banks, 1946, P. nigroprasina Haupt, 1952; P. seifferti Lucas, 1895 = P. cornuta Lucas, 1895, P. moebiusi Lucas, 1895, P. stygia Lucas, 1895; P. luteicornis Fabricius, 1804 = P. strenua Erichson, 1848, P. tinctipennis Smith, 1873, P. citreicornis Mocsáry, 1894, P. venosa Banks, 1945, P. alector Banks, 1946; P. asteria Mocsáry, 1894 = P. luridicornis Brèthes, 1926; P. convexa Lucas, 1895 = P. humeralis Brèthes, 1914; P. helvolicornis Lucas, 1895 = P. bahiae Brèthes, 1914; P. vitripennis Smith, 1855 = P. obscura Lepeletier, 1845, P. amabilis Mocsáry, 1885, P. centralis Cameron, 1893, P. margarete Lucas, 1895, P. venezuelae Kaye, 1913, P. aeneipennis Banks, 1946, P. helenae Haupt, 1952, P. coeruleoviridis Haupt, 1952; P. fumipennis Smith, 1855 = P. pallidicornis Mocsáry, 1885; P. amyntas Mocsáry, 1885 = P. vicina Lucas, 1895, P. clarinervis Brèthes, 1908, P. amyntoides Lucas, 1919, P. eurydice Lucas, 1919; P. dimidiata Fabricius, 1804 = P. vittigera Lucas, 1897, P. argentina Brèthes, 1908, P. sanctaeannae Brèthes, 1908, P. virgo Brèthes, 1908, P. externa Brèthes, 1908, P. transversa Brèthes, 1908, P. cordubensis Brèthes, 1908, P. banghaasi Lucas, 1919; P. menechma Lepeletier, 1845 = P. elegans Lepeletier, 1845, P. dubitata Cresson, 1867, P. prismatica Smith, 1855, P. advena Mocsáry, 1885, cinctipennis Mocsáry, 1885, P. guatemalensis Cameron, 1893, P. nestor Mocsáry, 1894, P. nigricornis Mocsáry, 1894, P. auranticornis Lucas, 1895, P. fruhstorferi Lucas, 1895, P. concolor Lucas, 1895, P. cerberus Lucas, 1895, P. euchroma Lucas, 1895, P. nigrocincta Lucas, 1895, P. mordax Lucas, 1895, P. inermis Fox, 1898, P. roberti Brèthes, 1908, P. janira Brèthes, 1908, P. cultrata Brèthes, 1908, P. novitia Banks, 1921; P. decipiens Lucas, 1895 = P. similis Lucas, 1895; P. minarum Brèthes, 1914 = P. pulchra Brèthes, 1914; P. basifusca Lucas, 1895 = P. angustimarginata Viereck, 1908; P. chrysoptera Burmeister, 1872 = P. exigua Lucas, 1895, P. smaragdinula Lucas, 1895, P. nebulosa Lucas, 1895, P. karschi Lucas, 1895, P. anisitsii Brèthes, 1908, P. indistincta Brèthes, 1908, P. dimidiatipennis Brèthes, 1908, P. chloroptera Brèthes, 1908, P. culta Brèthes, 1908, P. recta Brèthes, 1908, P. tornowii Brèthes, 1908, P. schrottkyi Brèthes, 1908, P. itinerata Brèthes, 1908, P. miniata Brèthes, 1908, P. spegazzinii Brèthes, 1908, P. paulistana Brèthes, 1914, P. chloe Brèthes, 1914, P. coronaria Brèthes, 1914, P. semilucana Haupt, 1952, P. bruneipes Haupt, 1952, P. brachynotus Haupt, 1952, P. diagonalis Haupt, 1952, P. discrepans Haupt, 1952; P. elongata Lepeletier, 1845 = P. purpurascens Smith, 1855, P. fuscipennis Smith, 1873, P. longula Banks, 1946; P. australis Saussure, 1867 = P. centaurus Lucas, 1897; P. cyanescens Lepeletier, 1845 = P. micans Mocsáry, 1885, P. jucunda Mocsáry, 1885, P. balloui Banks, 1946, P. diversa Haupt, 1952; P. lampas Lucas, 1895 = P. venturii Schrottky, 1902; P. nitida Lepeletier, 1845 = P. lucidula Smith, 1855, P. vaualba Smith, 1855, P. pruinosa Mocsáry, 1894, P. cylindrica Lucas, 1895, P. andina Brèthes, 1908, P. dilatata Brèthes, 1908, P. holmbergi Brèthes, 1908, P. concava Brèthes, 1908, P. ephebus Brèthes, 1908, P. vaga Brèthes, 1908, P. fuscobasalis Brèthes, 1908, P. cordata Brèthes, 1914, P. impatiens Brèthes, 1914, P. tricolor Brèthes, 1914, P. joergenseni Brèthes, 1914, P. cleone Brèthes, 1914, P. dorsata Brèthes, 1914, P. aretheas Brèthes, 1914, P. lassonis Lucas, 1819, P. consors Banks, 1946, P. interrupta Banks, 1946, P. analis Haupt, 1952; P. seladonica Dahlbom, 1843 = P. deuteroleuca Smith, 1855, P. kohli Lucas, 1895, P. venezolana Brèthes, 1908, P. burmeisteri Brèthes, 1908; P. cybele Banks, 1945 = P. weberi Banks, 1946; P. thoreyi Dahlbom, 1845 = P. lurida Lucas, 1895, P. euterpe Brèthes, 1908; P. flavescens Lucas, 1895 = P. periphetes Lucas, 1895, P. limbatella Brèthes, 1908, P. discoidalis Brèthes, 1914, P. limbatica Brèthes, 1914, P. militaris Brèthes, 1914, P. cavillatrix Haupt, 1952, P. arcuata Haupt, 1952, P. recterugosa Haupt, 1952, P. adversatrix Haupt, 1952; P. nigricans Lucas, 1895 = P. troglodytes Brèthes, 1908; P. montezuma Smith, 1855 = P. quitonensis Packard, 1869, P. sibylla Mocsáry, 1885, P. circe Mocsáry, 1885, P. occidentalis Cameron, 1893, P. peruanus Lucas, 1895, P. fulva Lucas, 1895, P. nessus Lucas, 1895, P. fusca Lucas, 1895, P. andicola Cameron, 1903, P. chilloensis Cameron, 1903, P. patagonica Brèthes, 1908, P. fasciculata Brèthes, 1908, P. pisoensis Strand, 1911, P. pacifica Brèthes, 1914, P. huascar Banks, 1946; P. completa Smith, 1855 = P. quichua Brèthes, 1908, P. comes Banks, 1946; P. smaragdina Dahlbom, 1843 = P. thunbergi Dahlbom, 1843, P. lara Mocsáry, 1888, P. satrapes Lucas, 1895, P. nupta Lucas, 1895, P. erynnis Lucas, 1895, P. fraterna Lucas, 1895, P. diabolus Lucas, 1895, P. mystica Lucas, 1895, P. thalia Brèthes, 1908, P. brasiliensis Brèthes, 1908, P. pallida Brèthes, 1908, P. iheringi Brèthes, 1908, P. dromeda Brèthes, 1908, P. sepultrix Lucas, 1919, P. strickeri Lucas, 1919; P. discolor Taschenberg, 1869 = P. sinnis Lucas, 1895, P. jujuyensis Brèthes, 1908, P. modesta Brèthes, 1908, P. comparata Brèthes, 1908, P. neutra Brèthes, 1908, P. terebrans Brèthes, 1908, P. procera Haupt, 1952, P. plaumanni Haupt, 1952, P. ogloblini Haupt, 1952, P. deletrix Haupt, 1952; P. limbata Guérin, 1831 = P. richteri Brèthes, 1908, P. polita Brèthes, 1908, P. limbella Haupt, 1952, P. artemis Haupt, 1952; P. basalis Mocsáry, 1885 = P. erdmanni Lucas, 1895, P. basinigra Haupt, 1952; P. infuscata Spinola, 1841 = P. niobe Mocsáry, 1885, P. sagana Mocsáry, 1894, P. incerta Banks, 1946; P. hyalinipennis Mocsáry, 1885 = P. subruficornis Haupt, 1952; P. festiva Fabricius, 1804 = P. pulchella Lepeletier, 1845, P. solitaria Smith, 1879, P. gallardoi Brèthes, 1908, P. hora Brèthes, 1914, P. amok Lucas, 1919, P. riojaneirensis Lucas, 1919; P. gracilis Lepeletier, 1845 = P. diana Mocsáry, 1885, P. hecate Mocsáry, 1885, P. spathulifera Lucas, 1895, P. sphinx Lucas, 1895, P. ierensis Banks, 1945, P. alceste Banks, 1946, P. scalaris Haupt, 1952; P. mildei Stål, 1857 = P. charon Mocsáry, 1885, P. cyanoptera Lucas, 1895, P. dryas Lucas, 1919; P. filiola Brèthes, 1914 = P. denserugosa Haupt, 1952; P. ruficornis Fabricius, 1804 = P. saphirus Palisot de Beauvois, 1805, P. violacea Mocsáry, 1885, P. hexamita Lucas, 1895, P. omniviolacea Haupt, 1952; P. brunneicornis Lucas, 1895 = P. glabripennis Lucas, 1895; P. purpurea Smith, 1873 = P. pan Mocsáry, 1885, P. parthenope Mocsáry, 1885, P. sagax Lucas, 1895, P. clypeata Brèthes, 1914, P. consimilis Banks, 1946, P. laconia Banks, 1946; P. viridisetosa Spinola, 1841 = P. eximia Smith, 1873; P. viridis Lepeletier, 1845 = P. errans Lepeletier, 1845, P. chlorotica Mocsáry, 1885, P. excelsa Lucas, 1895, P. selene Lucas, 1895, P. fimbriata Lucas, 1895, P. calypso Brèthes, 1908, P. fluminensis Brèthes, 1908, P. argentinicus Strand, 1910, P. mimetica Brèthes, 1914, P. garbei Brèthes, 1914, P. erecta Brèthes, 1914, P. tandilensis Brèthes, 1914, P. meridionalis Brèthes, 1914, P. minor Lucas, 1919, P. basifulgens Lucas, 1919, P. nebulosipennis Lucas, 1919, P. purpurea Lucas, 1919, P. koerberi Lucas, 1919, P. inimicissima Lucas, 1919, P. debilitans Lucas, 1919, P. itapaca Banks, 1946; P. aciculata Taschenberg, 1869 = P. nero Lucas, 1895; P. atripennis Fabricius, 1804 = P. flavilis Brèthes, 1908; P. ianthina Erichson, 1848 = P. fulvicornis Mocsáry, 1885, P. sirene Lucas, 1895, P. balboae Lucas, 1919, P. herodes Lucas, 1919, P. curti Lucas, 1919; P. nana Mocsáry, 1885 = P. mapiriensis Lucas, 1919, P. vinciens Lucas, 1919, P. ilione Banks, 1946, P. moesta Banks, 1946, P. orestes Banks, 1946, P. amautas Banks, 1946, P. inaequalis Haupt, 1952; P. hirtiventris Banks, 1946 = P. viridaurea Haupt, 1952, P. aequalis Haupt, 1952; P. auriguttata Burmeister, 1872 = P. aurimacula Mocsáry, 1885, P. flavicornis Mocsáry, 1894, P. guttata Lucas, 1895, P. incendiaria Lucas, 1895, P. pubiventris Lucas, 1895, P. planifrons Lucas, 1895, P. lestes Lucas, 1895, P. villosa Brèthes, 1908; P. sabina Mocsáry, 1885 = P. astioles Banks, 1946; and P. purpureipes Packard, 1869 = P. chlorana Mocsáry, 1885, P. antennalis Cameron, 1893, P. sulcifrons Cameron, 1903, P. carinata Brèthes, 1914, P. equatoriana Brèthes, 1914, P. angusta Banks, 1946. Keys to all forms are given. The mimicry-groups of P. atripennis Fabricius, 1804, and P. completa Smith, 1855, are defined and described and a comparative account of mimicry based on all four mimicrygroups in Pepsis is given. Lists of excluded species (with their current taxonomic placement and depository where ascertained), unplaced names, and a nomen nudum are given.
    Keywords: spider-hunting wasps ; Pompilidae ; Pepsis ; systematic revision ; new species ; mimicry ; Neotropical ; natural history ; 42.75
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  • 15
    facet.materialart.
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    In:  Zoologische Mededelingen (00240672) vol.78, 1-16 (2004) p.241
    Publication Date: 2015-06-03
    Description: A new species of the genus Allobracon Gahan, 1915, from Brazil is described and illustrated. It is the first green species of the genus and of the subfamily known. A key to the species is added.
    Keywords: Allobracon ; Hymenoptera ; Braconidae ; Hormiinae ; Brazil ; neotropical ; new species ; key ; green pigmentation ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 16
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.78, 1-16 (2004) p.181
    Publication Date: 2007-01-18
    Description: A supplement to the “Revision of the genus Paratropus Gerstaecker” (Kanaar, 1997) is given. Additional faunistic data are presented. The following four new species are described and figured: P. angulifrons (Malaysia: Sabah), P. strigosus (Cameroon, Ghana), P. tenuis (Indonesia: Sumatra) and P. transvalensis (South Africa: Transvaal).
    Keywords: Coleoptera ; Histeridae ; Paratropus ; Termitophiles ; Myrmecophiles ; Africa ; Oriental region ; new species ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 17
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.78, 1-16 (2004) p.123
    Publication Date: 2007-01-18
    Description: A new species of the genus Phaenocarpa Foerster (Hymenoptera: Braconidae: Alysiinae: Alysiini) from the Atlantic rainforest in Brazil is described and illustrated.
    Keywords: Braconidae ; Alysiinae ; Alysiini ; Phaenocarpa ; Neotropical ; Brazil ; atlantic forest ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 18
    Publication Date: 2007-01-18
    Description: The genus Mama Belokobylskij, 2000 (Braconidae; Euphorinae) is re-assessed and the type species is compared with three similar species: Microctonus cephalicus Provancher, 1886, Microctonus reclinator Ruthe, 1856, and Euphorus spiniscapus Muesebeck, 1936. The results are discussed in relation to the use of taxa based on one specimen (“monotype taxa”). Problems concerning our knowledge of important groups of Euphorinae are outlined. The context of the peculiarly tangled taxonomical situation, which this paper deals with, is considered to be widespread in parasitoid taxonomy, and should be borne in mind in current studies of parasitoid biodiversity assessment.
    Keywords: Mama Belokobylskij ; Microctonus cephalicus Provancher ; Euphorus spiniscapus Muesebeck ; Microctonus reclinator Ruthe ; monotypic genera ; monotype taxa ; biodiversity ; 42.75
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  • 19
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.78, 18-28 (2004) p.337
    Publication Date: 2007-01-18
    Description: Two new species of the genus Pambolus Haliday, 1836, (P. leponcei spec. nov., and P. pilcomayensis spec. nov.; Braconidae: Pambolinae) from Argentina are described and illustrated.
    Keywords: Braconidae ; Pambolinae ; Pambolus ; Neotropical ; Argentina ; new species ; partial key ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 20
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.78, 18-28 (2004) p.331
    Publication Date: 2007-01-18
    Description: Bitomoides gen. nov. (type species: Bitomus latus Papp, 1999) is described and illustrated. In addition Phaedrotoma recondes spec. nov. and Chelonus lukasi nom. nov. are validated.
    Keywords: Hymenoptera ; Braconidae ; Opiinae ; Bitomoides ; Orientopius ; Opius ; Phaedrotoma ; Microchelonus ; Chelonus ; Palaearctic ; Europe ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 21
    facet.materialart.
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    In:  Zoologische Verhandelingen vol.346 (2004) p.1
    Publication Date: 2007-01-22
    Keywords: Dirk Noordam ; in memoriam ; bibliography ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 22
    Publication Date: 2007-01-18
    Description: A new species of the genus Aleiodes Wesmael, 1838 (Braconidae: Rogadinae: Rogadini), A. declanae spec. nov. from New Zealand is described and illustrated. It has been reared from Declana floccosa Walker, Cleora scriptaria (Walker), Pseudocoremia suavis Butler and P. fenerata Felder & Rogenhofer (Geometridae: Ennominae.
    Keywords: Hymenoptera ; Braconidae ; Rogadinae ; Aleiodes ; New Zealand ; Australasian ; Oriental ; East Palaearctic ; new species ; distribution ; partial key ; Geometridae ; Ennominae ; Declana floccosa ; Pseudo-coremia suavis ; Pseudocoremia fenerata ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 23
    Publication Date: 2015-06-03
    Description: Goellneriana deckerti gen. nov. & spec. nov. (Heteroptera: Reduviidae: Phymatinae: Macrocephalini) from Namibia is described and illustrated. Keys to the tribes and to the Afrotropical genera and species of the subfamily Phymatinae are included, a checklist and a distribution map of the Afrotropical ambush bugs is added.
    Keywords: Insecta ; Heteroptera ; Reduviidae ; Phymatinae ; Goellneriana deckerti ; new genus ; new species ; Namibia ; list of Afrotropical Phymatinae ; distribution ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 24
    Publication Date: 2007-01-18
    Description: Three new species of the genera Megischus Brullé and Stephanus Jurine from China (Hymenoptera: Stephanoidea: Stephanidae) are described, illustrated and keyed. Megischus ptosimae Chao, 1964, from Fujian is redescribed and the specimen from India described as M. ptosimae Chao by van Achterberg (2002) is renamed as M. alveolifer spec. nov. and the Malaysian specimen of M. ducalis Westwood listed by van Achterberg (2002) is described as M. ducaloides spec. nov. M. ducalis Westwood, 1851, is reported for the first time from Cambodia, which is the first report after its description. A key to world species of the genus Stephanus is provided.
    Keywords: Hymenoptera ; Stephanoidea ; Stephanidae ; Megischus ; Stephanus ; China ; Oriental ; Palaearctic ; new species ; keys ; Buprestidae ; Cerambycidae ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 25
    Publication Date: 2007-01-18
    Description: The genus Taractrocera is distributed throughout the Oriental and Australian Regions. It contains 16 species, of which two, T. fusca and T. trikora, are described as new in this paper. All species are briefly characterized and the new species are described in full. The phylogeny of the genus is inferred, based on an analysis of morphological and genital characters, both of males and females. The biogeography of the genus is discussed in relation to the phylogeny. The genus has an Australian origin. After some diversification in Australia it dispersed into Asia, in or before the Miocene. It dispersed in the reverse direction, probably before the late-Miocene emergence of the Banda Arc and the Moluccas, 5-6 Mya. Three species are adapted to high altitude, one in the Himalayas and two in New Guinea. Apparently the adaptations occurred independently in the two areas. In New Guinea the high altitude species may have simply been carried up by the Pleistocene and recent uplift of the mountains. Possibly helped by the lowering of the sea-level several times during the Pleistocene, one Australian species colonized some of the Lesser Sunda Islands relatively recently.
    Keywords: Lepidoptera ; Hesperiidae ; Taractrocera ; systematics ; phylogeny ; biogeography ; Indo-australia ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 26
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen (00240672) vol.78, 18-28 (2004) p.291
    Publication Date: 2007-01-18
    Description: Neptihormius gen. nov. (type species Neptihormius stigmellae spec. nov. from New Zealand) is described and illustrated. It is a parasitoid of Nepticulidae and the first record of Nepticulidae as host for a member of the subfamily Hormiinae and of basal cyclostome Braconidae.
    Keywords: Hymenoptera ; Braconidae ; Hormiinae ; Neptihormius ; New Zealand ; new genus ; new species ; Australasian ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 27
    facet.materialart.
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    In:  Zoologische Mededelingen (00240672) vol.78, 18-28 (2004) p.313
    Publication Date: 2007-01-18
    Description: Two new subgenera of the genus Xynobius Foerster, 1862, from the Southern Hemisphere are described and illustrated: Paraxynobius (type species Xynobius granulatus spec. nov. from New Zealand), and Sulcynobius (type species X. latisulcus spec. nov. from Sulawesi). One new species of the genus Ademoneuron Fischer, 1988, is added: A. yasirae spec. nov. from Indonesia (Halmahera).
    Keywords: Hymenoptera ; Braconidae ; Opiinae ; Xynobius ; Paraxynobius ; Sulcynobius ; Atormus ; Ademoneuron ; New Zealand ; Indonesia ; Sulawesi ; Halmahera ; new subgenus ; new species ; Australian ; Wallacean ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 28
    Publication Date: 2007-01-18
    Description: The venom apparatus of Pseudoyelicones nigriscutum van Achterberg, 1997 (Braconidae: Rogadinae) is described and illustrated. The venom apparatus morphology of Pseudoyelicones is closely related to that of Bulborogas van Achterberg. Therefore, we propose a sister group relationship between these two genera.
    Keywords: Pseudoyelicones ; venom apparatus ; Bulborogas ; Yelicones ; phylogeny ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 29
    facet.materialart.
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    In:  Zoologische Mededelingen (00240672) vol.78, 1-16 (2004) p.1
    Publication Date: 2007-01-18
    Description: The species of the genus Euagathis Szépligeti, 1900 (Braconidae: Agathidinae) from Wallacea and Papua (including Northeast Australia and Solomon Islands) are revised and keyed. Thirty-three species are recognized, of which 11 are new: Euagathis brevitibialis spec. nov. from Papua New Guinea; E. dejongi spec. nov. from Indonesia (Sulawesi); E. fuscistigma spec. nov. from Papua New Guinea; E. kendariensis spec. nov. from Indonesia (Sulawesi); E. maculata spec. nov. from Papua New Guinea; E. mellifacies spec. nov. from Papua New Guinea (Bougainville Island); E. mellisoma spec. nov. from Indonesia (Papua); E. minutoides spec. nov. from Indonesia (Sulawesi); E. novabritanica spec. nov. from Papua New Guinea (New Britain); E. raymondi spec. nov. from Indonesia (Papua); and E. toxopeusi spec. nov. from Indonesia (Papua). Euagathis maculipennoides nom. nov. is a new name for Euagathis maculipennis Szépligeti, 1902, not Brullé, 1846. Agathis etnaella Cameron, 1907, is a new synonym of Cremnops variceps (Cameron, 1907) and Euagathis papua Cameron, 1906, of E. novaguineensis Szépligeti, 1900. New combinations are: Biroia cameroni (Enderlein, 1920); Cremnops papuana (Cameron, 1907); C. varipilosella (Cameron, 1911); C. variceps (Cameron, 1907); and Zelomorpha maculipes (Cameron, 1911).
    Keywords: Braconidae ; Agathidinae ; Disophrini ; Euagathis ; key ; distribution ; synonyms ; Indo-Australian ; Oriental ; Sulawesi ; Moluccas ; New Guinea ; Papua ; Australia ; 42.75
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  • 30
    facet.materialart.
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    In:  Zoologische Mededelingen (00240672) vol.78, 1-16 (2004) p.77
    Publication Date: 2015-06-03
    Description: Six new genera of the family Braconidae (Hymenoptera) from China are described and illustrated: two genera of the subfamily Agathidinae: Facilagathis gen. nov. (type species: F. spinulata spec. nov.) and Cremnoptoides gen. nov. (type species: Cremnops pappi Sharkey, 1994); one genus of the subfamily Helconinae: Mangshia gen. nov. (type species: M. elongata spec. nov.); two genera of the subfamily Pambolinae: Plesiocedria gen. nov. (type species: P. intermediata spec. nov.) and Apocedria gen. nov. (type species: A. nodifer spec. nov.) and one genus belonging to the subfamily Opiinae: Opiolastes gen. nov. (type species: O. hei spec. nov.). In addition two new species are described: Facilagathis macrocentroides spec. nov. from Zhejiang and Cremnoptoides furcatus spec. nov. from Jilin.
    Keywords: Braconidae ; Agathidinae ; Agathidini ; Disophrini ; Helconinae ; Pambolinae ; Cedriini ; Pambolini ; Opiinae ; Opiini ; Facilagathis ; Cremnoptoides ; Mangshia ; Apocedria ; Plesiocedria ; Opiolastes ; key ; distribution ; Oriental ; Palaearctic ; China. ; 42.75
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  • 31
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    In:  Nederlandse Faunistische Mededelingen (01692453) vol.11 (2000) p.19
    Publication Date: 2007-01-10
    Description: New and lesser-known amphipods of hard substrates in the Delta area of the Netherlands (Crustacea: Amphipoda: Gammaridea) The distribution of 27 new and lesser-known amphipod species of sublittoral hard substrates in the Delta area in the southwest of The Netherlands is described. Data from literature on these species are scarce and/or not readily available. They are supplemented with results from recent investigations of mainly sublittoral hard substrates. Of the 22 marine species only nine occur offshore as well as inshore. The others seem to be restricted to inshore man-made coastline protections. This probably reflects the scarcity of hard substrates further offshore. Four invasive species were recorded in the brackish and freshwater part of the Delta area, two of them of pontocaspian origin.
    Keywords: Arthropoda ; Amphipoda ; Gammaridea ; Nederland ; Verspreiding ; Biotopen ; Herkenning ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 32
    facet.materialart.
    Unknown
    In:  Nederlandse Faunistische Mededelingen (01692453) vol.11 (2000) p.45
    Publication Date: 2007-01-10
    Description: The expansion of the range of the spider Argiope bruennichi in the Netherlands (Araneae: Araneidae) Argiope bruennichi (Scopoli, 1772) is one of the biggest and most colourful spiders in Europe and therefore easy to recognise, even by non-specialists. The species has expanded its range in Germany and Belgium for several decades now and reached the south of The Netherlands in 1980. After the discovery of the first female in the south of the province of Limburg more specimens were found in this region in subsequent years. Later the species was discovered near Herkenbosch, about 30 kilometres to the north. Over the last years the expansion continued rapidly and now almost 300 records are brought together. The species has become widespread in the southern and eastern part of The Netherlands. In 1995 a leap of some 70 kilometres was made, from Limburg to the southern parts of the Veluwe. The years 1998 and 1999 were very good for Argiope, both with over 80 records per year. It is suggested that this expansion is related to the warm and sunny summers in the nineties.
    Keywords: Arthropoda ; Araneae ; Araneidae ; Argiope bruennichi ; Wespenspin ; Wespspin ; Tijgerspin ; Nederland ; Verspreiding ; Biotopen ; Uitbreiding ; Fenologie ; 42.75
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  • 33
    Publication Date: 2007-01-10
    Description: Nests of the carpenter ant Camponotus ligniperda in the northwestern part of its range (Hymenoptera: Formicidae) Camponotus ligniperda (Latreille, 1802) is a rare ant species restricted to the eastern part of the Netherlands. Most records relate to a low number of workers. In this paper the species is reported for the first time from the province of Drenthe. Some ecological features of the groundnest are compared with the only other recent nest in the Netherlands. Both nests are located under a decidious tree which protects them from excessive precipitation. In contrast with reports from Germany and Sweden, nesting sites in buildings and houses are not known. It is suggested that the low chances for settlement in our country are due to the wet atlantic climate as well as competition with larger Formica species.
    Keywords: Insecta ; Hymenoptera ; Formicidae ; Camponotus ligniperda ; Nederland ; Verspreiding ; Biotopen ; 42.75
    Repository Name: National Museum of Natural History, Netherlands
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  • 34
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 67 (1984), S. 47-53 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The He(Iα) photoelectron (PE) spectra of tris(perfluorocyclobuta)benzene 4(F)3,3,4,4,7,7,8,8,11,11,12,12-Dodecafluorotetracyclo[8.2.0.02,5.06,9]dodeca-1,5,9-triene, tris(perfluorocyclopenta)benzene 5(F)1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9-Octadecafluoro-2,3,4,5,6,7,8,9-octahydro-1H-trindene., tetrakis(perfluorocyclobuta)cyclooctatetraene 6(F)3,3,4,4,7,7,8,8,11,1l,l2,l2,l5,15,16,16-Hexadecafluoropentacyclo[12.2.0.02,5.06,9.010,13]hexadeca-1,5,9,13-tetraene., and of tetrakis(perfluorocyclopenta)cyclooctatetraene 7(F)1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12-Tetracosafluoro-1,2,3,4,5,6,7,8,9,10,11,12-dodeca-hydrotetracyclopenta[a,c,e,g]cyclooctene. are reported. A tentative assignment of the PE spectra is derived by empirical correlation with those of relevant reference compounds. The results suggest that 6(F) retains the D4h-conformation in the gas phase, i.e. A conformation with a planar cyclooctatetraene ring, as observed in the crystal. All four compounds exhibit a sharp increase of their first ionization energies, relative to the corresponding parent hydrocarbons, due to the perfluoro effect.
    Additional Material: 1 Ill.
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  • 35
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ligand 2,11-bis(diphenylphosphinomethyl)benzo[c]phenanthrene (1) has been used to prepare complexes of the type [PtL(1)] (L = C2H4, CH2=CH—CO2Me, PhC≡CPh, MeC≡CMe, MeO2CC≡CCO2Me, (i-Pr)O2CC≡CCO2(i-Pr), Ph3P and CO). It is shown that these complexes are less labile than the corresponding species [PtL(Ph3P)2]. The preparation of complexes trans-[PtX(R)(1)] by oxidative addition of RX (RX = PhCH2Br and Mel) to [Pt(C2H4)(1)] is described. The isolation of [PtO2(CH3)2CO(1)] is also reported.
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  • 36
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical anions of the compounds N1N, N3N and N5N, in which two naphthalen π-systems are separated by 1, 3 and 5 spirobonded cyclobutane rings, respectively, and tha tof the reference compound N1, containing one naphthalene π-system and one cyclobutane ring, have been studied by ESR and ENDOR spectroscopy under a variety of experimental conditions. The intramolecular electrons spin transfer between the two π-moieties in N3N.⊖ and N5N.⊖ is slow on the hyperfine time-scale, irrespective of the applied conditions. It is also slow in N1N.⊖, except for media of high solvating power. In such media, with a slight reduction of N1N to its radical anion, a paramagnetic species is observed, the hyperfine data for which are consistent with N1N to its radical anion, a paramagnetic species is observed, the hyperfine data of which are consistent with N1N.⊖, undergoing a fast intramolecular electron spin tansfer. The ESR and ENDOR spectra of this species are superimposed on those characteristic of a slow transfer. It is suggested that the fast and slow transfer involve the syn- and anti-conformations, respectively, since the distance, r, between the two naphthalene π-systems of N1N.⊖ is considerably shorter in the former than in the latter (r = 740 vs. 880 Pm for the distance between the centres of the π-systems). Glassy solutions of exhaustively reduced N1N display signals of the dianion triplet state, whereas no such signals are found for N3N and N5N. The zero-field splitting parameter, D, is 4.7 mT, corresponding to r ≈ 480 pm.
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  • 37
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Loss of CH3., CH4, C2H4, C3H5., C3H6 and C3H7 from the molecular ions of a number of 13C-labeled analogs of 4,4-dimethyl-1-pentene was studied both in normal (source) 70-eV electron impact (EI) spectra dn in metastable spectra. For loss of CH3. in the source, 96% of the methyl comes frm positions of 5, 5′ and 5″, while the remainder comes from position 1. In the metastable spectra, loss of C-1 (16%) and C-3 (9%) is increasing in importance. The loss of ethylene is a particular case: either C-1 or C-3 are lost with any other C-atom from positions 2,5,5′, and 5″ (8 × 10%) in the metastable spectra, the probability for simultaneous loss of C-1 and C-3 being 6%. If C-1 seems to these two positions become completely equivalent in the metastable time range. The T-values (kinetic energy release) for the different positions show small, but statisticaly different values and a small isotope effect. Loss of C3H5 (allylic cleavage) is 100% C-1, C-2 and C-3, i.e., no evidence for skeletal rearrangement is seen. This is also true for loss of C3C6 (McLafferty rearrangement) within the source, but in metastable decay the other positions gain in importance. The neutral fragment C3H7. appears to be the the result of consecutive loss of CH3. and C3H4, rather than a one-step loss of propyl radical or the inverse reactions sequence. No metastable reaction can be seen for this reaction. Decomposition of labeled C6H11+ and C5H10+ secondary ions occurs in an essentially random fashion.
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  • 38
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    Helvetica Chimica Acta 67 (1984), S. 450-454 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Up to now the synthesis of para-substituted phenyl-terpyridine ligands was difficult with respect to the purification of the reaction products. We have found that these compounds can easily be isolated as hydrobromides from acetic acid. Starting from the hydrobromides the purification turned out to be easy. Synthesis of para-substituted Cl-, Br-, H3C-, H2BrC-, HO- 2,6-Bis(2-pyridyl)-4-phenylphyridine is reported.
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  • 39
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    Helvetica Chimica Acta 67 (1984), S. 441-449 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexation of Silver(I) by Cyclic TetraminesThe nature of Ag(I)-complexes with 1,4,8,11-tetraazacyclotetradecane (1), 1,5,9,13-tetraazacyclohexadecane (2) 1,5,10,14-tetraazacyclooctadencane (3) and 1,6,11,16-tetraazacycloeicosane (4) is studied. The effect of ring size on disproportionation of the Ag() cation in the presence of ligand is reported. The stability of Ag(I)-complexes with 3 and 4 in aqueous solution is determined by means of potentiometric titration.
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  • 40
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    Helvetica Chimica Acta 67 (1984), S. 625-627 
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    Keywords: Chemistry ; Organic Chemistry
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  • 41
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    Helvetica Chimica Acta 67 (1984) 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 42
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    Helvetica Chimica Acta 67 (1984), S. 625-639 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical Ions of Bridged [14] Annulenes. Investigations on the Influence of Frontier Orbitals on Reactivity and BondingThe radical anions and the radical cations derived from trans-15, 16-dimethyl-1, 4:8,11-ethandiyliden[14]annulene (6), trans-15-methyl-1,4:8,11-ethandiyliden[14]annulene (7) and cis-15, 16-propano-1,4:8,11-ethandiyliden[14]annulene (8) are described. The hyperfine data of the radical anions 6, 7 and 8 resemble those of the structurally related radical anions of trans-10b, 10c-dimethyldihydropyrene (4) and trans-10b, 10c-dihydropyrene (5). This finding leads to the conclusion, that the change in the relative arragement of the saturated bridge within the fourteen-membered π-perimeter by passing from 4 (5) to 6 (7, 8) does not in fluence the energetic sequence of the lowest unoccupied molecular orbitals. The behavior of 6 and 7 towards oxidation parallels the photochemical reactivity of 4. The hyperfine coupling constants of the radical cations derived from 6 and 7 indicate that the removal of an electron is accompanied by an isomerization of the molecular framework. The investigation of the electron transfer process gby cyclic voltammetry supports these findings. The radical cations prefer the cyclophane-like structures 6a and 7a, in which the central σ-bond (C(15)-C(16) bond) is broken.
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  • 43
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    Helvetica Chimica Acta 67 (1984), S. 664-668 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photochemical behaviour of the title compound 1a is compared to that of the non-fluorinated parent ketone 2-methylcyclohexanone (1b). Substitution of the CH3- group on C(2) by a trifluoromethyl group strongly enhances 2H- and RH- reduction product formation in cyclohexane or 2-propanol and oxetane formation in the presence of 2-methylpropene as olefinic component. Under all these conditions 1b exclusively undergoes a-cleavage, a process observed for 1a only in non-reducing solvents as benzene or tert-butyl alcohol.
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  • 44
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of β-keto-acetals, derived from non-enolisable β-diketones, with sulfonic acids in boiling benzene resuots in a smooth retro-Claisen-type fragmentation. The acetal-C-atom is thereby transformed into a carboxylic ester via a dialkoxycarbenium ion, which is dealkylated by the sulfonate counter-ion. Application of this reaction to the diastereomeric monoacetals 3 and 4, derived from cis-9-methyl-decalin-1,8-dione (1), followed by transesterification with CH3OH, yields optically pure 4-(2′-methyl-3′-oxocyclohexyl)butyrate 9 ((+)-9 from 3, (-)-9 from 4) and the monosulfonate of Meso-2,3-butanediol (-)-13 (Scheme 2). Unexpectedly, this cleavage proceeds as well with monoacetal 26, obtained by acetalization of trans-9-methyl-decalin-1,8-dione (27) with 2,2-dimethyl-1,3-propanediol (Scheme 7). Some attempts, aiming at an isomerization of the cis- and trans-decalin derivatives 3 and 24, or 25 and 26, via the postulated carboxonium intermediate, were not successful.
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  • 45
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    Helvetica Chimica Acta 67 (1984), S. 856-865 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkylation of bicyclo[3.3.0]octane-2,8-dione (1), which is prepared by a modification of the procedure described in the literature, gives the methyl- and propynyl-derivatives 6 and 7 (Scheme 1). In addition to the method described previously (Scheme 2), 9-methyl-cis-decalin-1,8-dione 9 is obtainable stereoselectively either by cyclization of keto-acid 16, or by aldol cyclization of keto-aldehyde 26 and oxydation of the resulting alcohols 24 and 25 (Scheme 4). The β-keto-alcohols 24 and 25 undergo a base-catalyzed isomerization; the trans-decalin isomers 27 and 28 are not detected in this equilibrium mixture (Schemes 4 and 5)l. Monoreduction of cis-dione 9 gives the endo-alcohol 25, while 27 is the favored product of the reductin of trans-dione 10 (Scheme 4). Optically pure (+)-25 can be prepared from (9S,10R)-monoacetal 29 (Scheme 5).
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  • 46
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new tripeptide (dimer), bis[(L-cysteine-S-acetyl)-L-hemicystinyl(S2 → S2)-D-valine] (6) was synthesized by coupling N-(tert-butoxycarbonyl)-S-carboxymethyl-L-cysteine benzyl ester (1) with S-trityl-L-cysteinyl-D-valine benzyl ester and subsequent removal of the protecting groups. After reduction of the disulfide, the free tripeptide Cys (CH2CO-Cys-D-Val) (Ib) was used as a substrate of isopenicillin-N synthetase in a cell-free conversion to 6-[2-((D-2-amino-2-carboxyethyl)thio)acetamido]penicillanic acid (IIa).
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  • 47
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    Helvetica Chimica Acta 67 (1984), S. 902-905 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the title compounds is described.
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  • 48
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    Helvetica Chimica Acta 67 (1984), S. 927-927 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 49
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Resolution of racemic cis-3-(2-aminophenylthio)-2-hydroxy-3-(4-methoxyphenyl) propionic acid (2) via the cinchonidine salt 3, and brucine salt 4, isolation of the calcium salts (+)- and (-)-5, as well as their cyclization to enantiomeric 1,5-benzothiazepines (+)- and (-)-1, are described. X-Ray single-crystal analysis reveals (2S, 3S) absolute configuration of (+)-1 on the basis of tentative comparison of CD data with those for the 1,4-benzodiazepine derivative (+)-8 of known absolute configuration.
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  • 50
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    Helvetica Chimica Acta 67 (1984) 
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  • 51
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    Helvetica Chimica Acta 67 (1984), S. 927-933 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis ad Structure of Zinc Complexes of 2-Amino-1-azetinesThe 2-dimethylamino-3,3-dimethyl-1-azetines 7a and 7b have been synthesized in analogy to the procedure reported by Ghosez et al. [1] (Scheme). The crystal structure of 1-benzhydryl-azetidindimethyliminium chloride 5a, a precursor of azetine 7a, has been established by X-ray diffraction analysis. Treatment of azetines 7a and 7b with ZnBr2 in CH2Cl2/MeCN yielded tetrahedral bis (azetine)dibromozinc complexes 8a and 8b, respectively (Scheme 2). The molecular structure of 8a has been determined by X-ray diffraction analysis too.
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  • 52
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    Helvetica Chimica Acta 67 (1984), S. 947-952 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantioselective synthesis of (+)- and (-)-cis-2-methyl-4-propyl-1,3-oxathine 8 and 9 form (E)-2-hezen-1-ol (1) as common starting material is described. The two enantiomeric forms exhibit different organoleptic properties.
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  • 53
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    Helvetica Chimica Acta 67 (1984), S. 959-963 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyanothyl-subsituted cylohexyl cyclohexanoates, bi(cyclohexanes) and phenyl cyclohexanes were synthisized. Their mesmorphic behaviour is compared to that of the corresponding cyano derivatives. (Cyanoethyl)cyclohexyl cyclohenxanoates show mesmorphic properties in contrast to the corresponding cyano derivative. Separation of the cyano substituent from the rigid core of an anisotropic aliphatic compound by methylene groups enhances the thermodynamic stability of the mesophase. In aromatic compound, the cyanoethyl group leads to lower clearing points. These phenomena are attributed to teh influence of steric effects on the packing density and to the dependence of the clearing point on molecular association.
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  • 54
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    Helvetica Chimica Acta 67 (1984), S. 1000-1002 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nα-L-Iysine with a 2-carboxy-4, 6-dinitrophenyl (Dncp) haptenic group on the ε-amino function is a potent anaphylactogen in the guinea pig. We prepared Nε -Dncp- Nα-benzoly-L-Iysinamide and Nε-Dncp-Nα-benzoyl-L-lysyl-1-aminopropane where the carboxyl group of Iysine is blocked. Both compounds were non-elections of anaphylaxis.
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  • 55
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    Helvetica Chimica Acta 67 (1984), S. 21-28 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: C45- and C50-Carotenoids. Synthesis of Optically Active Acyclic C15-End GroupsThe optically active C15-end groups (S)-12, (S)-13 and (R)-14 were prepared from the C12-synthon (S)-11 in good chemical and optical yield. These C15-end groups are suitable compounds for the synthesis of optically active C45- and C50-carotenoids.
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  • 56
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    Topics: Chemistry and Pharmacology
    Notes: In the crystal structure of the title compound at 98 K the dimethylamino group has pyramidal geometry. The nitrogenlone pair is not directed towards the triple bond; instead, one N—CH3 bond lies almost in the plane of the disubstituted ring, directed away from the triple bond, while the other N—CH3 bond and the lone pair are directed to opposite sides of the plane, nearer to the acetylene. There is a remarkably short intramolecular contact (2.39 Å) between a methyl H- and an acetylenic C-atom. The Taft σI parameter of the arylethynyl substituent appears to be similar to that of a carboxylic ester, judging from the bond-angle deformation at the ipso-C-atom.
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  • 57
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    Topics: Chemistry and Pharmacology
    Notes: The Heart Glycosides of the Arrow Poison of Lophopetalum toxicum LOHERFrom the cytotoxic and positive inotropic acting bark extract of the Philippinan Lophopetalum toxicum eight heart glycosides have been isolated and their structures have been elucidated mainly by field-desorption-MS- and 1- and 13C-NMR spectroscopy. Besides the known k-Strophanthidin (1), Antiarigenin (6) and β-Antiarin (Antiarigenin-3-β-O-α-L-rhamnoside, 10) the following mono- and diglycosides could be identified: strophanthidin-3-β-O-α-6-desoxy-D-allopyranoside (strophalloside, 2), strophanthidin-3-β-O-β-6-desoxy-D-glucopyranoside (= Strophanthidin chinovoside, 3), strophanthidin-3-β-O[-4Oβ-D-allopyranosyl-β-6-desoxy-D-allopyranoside] (4), strophanthidin-3-β-O-[3-O-β-D-glucopyranosyl-β-6-desoxy-D-talopyranoside] (5), antiarigenin-3-β-O-[3-O-β-D-gulopyranosyl-β-6-desoxy-D-talopyranoside] (7), antiarigenin-3-β-O-[4O-β-D-allopyranosyl-β-6-desoxy-D-allopyranoside] (8), and antiarigenin-3-β-O-β-6-desoxy-D-allopyranoside (antiallosid) (9). The structure of strophanthidinchinovoside (3) could be confirmed by synthesis.
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  • 58
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    Topics: Chemistry and Pharmacology
    Notes: A recent controversy on the interpretation of the ESR spectrum of ionized oxirane is clarified on the basis of the electronic absorption spectra of ionized tetramethyloxirane and 9,10-octalineoxide. The results favour a ring-opened structure for oxirane molecular cation, resulting from C—C bond cleavage and being iso-π-electronic to allyl radical.
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  • 59
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    Topics: Chemistry and Pharmacology
    Notes: The Acylation of Acetylenes with β,γ-Unsaturated Acid Chlorides, A New Synthesis of 5-Substituted 2-CyclopentenonesThe acylation of acetylenes with α,α-disubstituted, β,γ-unsaturated acid chlorides under Friedel-Crafts-type conditions leads to 5-substituted 2-cyclopentenones. Phenols are formed with β,γ-unsaturated acid chlorides bearing at least one α-H-atom. These transformations are explained by the intramolecular cyclization of the initially formed vinyl cation, which, in the cases of α,α-disubstituted acid chlorides, is followed by ring contraction. The reaction leading to 2-cyclopentenones is applied to the synthesis of some spiro[4.4]nona- and spiro[4.5]deca-2,6-dienones.
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  • 60
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    Helvetica Chimica Acta 67 (1984), S. 113-119 
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    Keywords: Chemistry ; Organic Chemistry
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    Topics: Chemistry and Pharmacology
    Notes: 1-Arylazonaphthalenes with all the potential cyclopalladation sites (one peri- and three ortho-positions) substituted by methyl or ethyl groups react with stoicheiometric or catalytic amounts of sodium tetrachloropalladate(II) to the corresponding 2-arylbenzo[g]indazoles. Possible mechanisms for the catalytic cyclization reaction are proposed.
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  • 61
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    Topics: Chemistry and Pharmacology
    Notes: 1n, π*-Excitation of the γ,δ-epoxy-enone (E)-3 leads exclusively to the conformers (Z)-3A + B. On 1π, π*-excitation of (E)-3, in addition to (Z)-3A + B, products 6-9 arising from a carbene intermediate e are formed. However, products of an isomerization via C(γ), O-bond cleavage of the oxirane were not formed on either mode of excitation. On thermolysis, at 80° the conformer (Z)-3A is transformed into (Z)-3B, which on photolysis returns to (Z)-3A and (E)-3. At 160°, however, (Z)-3B rearranges to the isomers 6, 10 and 11.
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    Helvetica Chimica Acta 67 (1984), S. 866-869 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Selective oxidation of benzylic methylene groups through UV irradiation in acetone/water/FeCl3 mixtures is reported. This method applied to a series of model compounds, provides an easy access to the corresponding 1-oxo derivative. Thus, tetralin gives a 100% yield of 1-tetralone, indane leads to 60% of 1-indanone, and diphenylmethane is oxidized to benzophenone with 80% yield. However, under the same conditions, alkyl-substituted aromatic hydrocarbons such as toluene, ethyl- and propylbenzene lead to low yields of aldehydes or ketones. Isochromane furnishes a mixture of two substances which can be interconverted, namely the expected l-isochromanone (9%) and the corresponding hydroxy acid (23%). We failed to apply the method to nitrogen heterocycles containing benzylic groups such as 1,2,3,4- and 5,6,7,8-tetrahydroquinoline as they do not react due to the formation of complexes which precipitate from the solutions.
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  • 63
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    Topics: Chemistry and Pharmacology
    Notes: Pure pencillin N α-sulfoxide (1) and penicillin N β-sulfoxide (2) were obtained by HPLC and tested as substrates for deacetoxycephalosporin C synthetase (DXCS). Neither one of the sulfoxides was utilized under conditions of conversion of penicillin N (8) to deacetoxycephalosporin C (9). The cephalosporin C α and β-sulfoxides (3 and 4, resp.) were also prepared. Relative stabilities of the sulfoxides 3 and 4 are discussed by interpretation of the 13C-NMR spectra.
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  • 64
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    Notes: The Business C,D,E,F,G,H,J,K,L und M, Ten New Tetranortriterpenes from Entandrophragma Bussei HarmsTen new tetranortriterpenes, busseins C, D, E, F, G., H, J, K, L and M have been isolated from the petroleum ether extract of the timber of Entandrophragma bussei Harms. utilizing separation by high-pressure liquid chromatography (HPLC). The structural assignments are based mainly on spectral evidence. For the 1H-NMR spectroscopy extensive use of nuclear Overhauser effects (NOE) was made.
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  • 65
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    Helvetica Chimica Acta 67 (1984), S. 928-930 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 66
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    Keywords: Chemistry ; Organic Chemistry
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    Topics: Chemistry and Pharmacology
    Notes: Alcohols and phenols are efficiently nitrated with thionyl chloride nitrate or thionyl nitrate, even in the presence of an aromatic moiety. While thionyl chloride nitrate is suitable for nitration of primary OH-groups in carbohydrates, thionyl nitrate is reactive enough to react with secondary OH-groups as well. These reagents permit the highly selective nitration of the 5′-,2′5′- and 3′, 5′-OH-groups of ribonucleosides to produce either mono-or diprotected nitro derivatives in high yields. Carbon acids and the enol form of some ketones are efficiently nitrated with trifluoromethanesulfonyl nitrate/potassium tert-butoxide. Lutidine N-oxide (2,6-(CH3)2C5H3N O) was found to have a marked effect on nitration reactions. Similarly, thionyl chloride nitrite and thionyl nitrite exhibit an excellent capacity for nitrosation of the aforementioned substrates.
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  • 67
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    Helvetica Chimica Acta 67 (1984), S. 934-938 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical cations and the radical of 1,2-bis(phenalen-1-ylidene)ethane (1), 1,2-bis(phenalen-1-ylidene)ethene (2) and pentaleno[1,2,3-cd: 4,5,6-c′ d′]diphenalene (3) have been characterized by ESR and ENDOR spectroscopy. The ease of formation of these radical ions and their π-spin distributions are interpreted in terms of a simple model correlates the frontier orbitals of 1, 2 and 3 with the nonbonding MO's of two phenalenyl π-systems.
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  • 68
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    Helvetica Chimica Acta 67 (1984), S. 939-946 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of 1-(2-propynyl)pyridinium salts 3 described. Compounds 3 react with a second pyridine molecule, in the presence of the corresponding hydrochloride, to form products of type 4, Certain bases cause the 1-(2-propynyl)pyridinium salts 3 to rearrange into 1-propadienylpyridinium salts. 5. Diethylamine converts compounds 3 into 1-acetonylpyridinium salts 8. Moreover, treatment of 3 or 5 with sodium methoxide gives enol ether sof type 9, which can be hydrolyzed to teh ketones 8. Addition of bromine to some of teh unsaturated compounds is also reported.
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  • 69
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    Helvetica Chimica Acta 67 (1984), S. 953-958 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: IR-spectroscopic investigations of light-induced rearrangement reactions of nitrosooxymethane (CH3ONO3), nitrosooxyethane (CH3CH2ONO) and N,N-dimethylnitrosamine ((CH3)2NNO) in low-temperature rare-gas matrices have established that these molecules are transformed in two photolysis steps to the previously unknown C-nitroso compounds nitrosomethanol (CH2(OH)(NO)), 1-nitrosoethanol (CH3CH(OH)(NO)), and methyl(nitrosomethyl)amine CH2(NO)(NH)(CH3). Evidence for a similar rearrangement reaction has been advanced for N-Nitrosopyrrolidine which is converted to C-nitrosopyrrolidine . The matrix-isolation technique in combination with wavelength-selective irradiation allowed to trap and characterize an intermediate of rearrangement which revealed to be nitroxyl (HNO) complex (CH2…HNO, CH3CHO…HNO, CH3N = CH2…HNO, and ). Since these findings have a close resemblance with rearrangement reactions of more complex nitrosooxy compounds, nitrosamines, or nitrosohydrazines used in organic synthesis, it is suggested that also in these reactions nitroxyl is present as an intermediate species.
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  • 70
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    Helvetica Chimica Acta 67 (1984), S. 964-967 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Epoxycarotenoids: Isolation of 1,2-Epoxy-1,2-dihydrolycopene from TomatoesThe optically active, 1,2-epoxy-1,2-dihydrolycopene was isolated from tomatoes. Its constitution was established by comparison with the racemic synthetic compound.
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  • 71
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Epoxycarotenoids: Synthesis, 1H-NMR and CD Studies of (S)-1,2-Epoxy-1,2-dihydrolycopene and (S)-1′,2′-Epoxy-1′, 2′ -dihydro-γ-caroteneThe synthesis of (S)-1,2-epoxy-1,2-dihydrolycopene ((S)-1) and (S)-1′, 2′ -epoxy- 1′, 2′ -dihydro-γ-carotene ((S)-2) are described. The CD spectra of the (all-E)-isomers and of the isomers (7Z, S)-1 and (7′Z, S)-2 are discussed. The comparison of the CD spectra of the synthetic (S)-1 and the compound isolated from the tomatoes proves the (S)-configuration of the natural product.
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  • 72
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    Helvetica Chimica Acta 67 (1984), S. 1003-1011 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Plectranthons A, B, C, and D. Diterpenoid Phenanthrene-1,4-diones from Leaf-glands a Plectranthus sp. (Labiatae)The following structures of four new 1,4-phenanthraquionones, isolated in minute amounts from the coloured leaf-glands of a Plectranthus sp. obtained from the borders of Lake Kiwu2, Rwanda, are proposed: plectranthon A (1; 3-hydroxy-5, 7,8-trimethyl-2-(2-propenyl)phenanthrene-1, 4-dione), plectranthon B (2; 2-(2ξ-acetoxypropyl)-3-hydroxy-5,7,8-trimethylphenanthrene-1,4-dione), plextranthon C (3; 3-hydroxy- 7,8-diemethyl-2-(2-propenyl)phenanthrene-1,4-dione), and plectranthon D (4; 3-hydroxy-7,8,10-trimethyl-2-(2-propenyl)phenanthrene-1,4-dione). 2-(2ξ-Hydroxypropyl)-3,6-dihydroxy-5,7,8-trimethylphenanthrene-1,4-dione (11), a compound very similar to 1-4, was prepared by a Wagner-Meerwein, rearrangement of coleon E (5). Biogenetically, the plectranthons are derived from abietanoic precursors. The compounds 1, 2 and 4 are the first natural C20-phenanthrenes of diterpenoid origin.
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  • 73
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    Keywords: Chemistry ; Organic Chemistry
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    Topics: Chemistry and Pharmacology
    Notes: Oxidative hydroboration of exo- (1) and end-Fe(CO)3 (2) complexes of 5,6-dimethylidenebicyclo[2.2.2]oct-2-ene are highly stereoselective and give endo -alcohol 3 and exo -alcohol 4 as major products, respectively, Collins oxidations of 3 and 4 furnish the corresponding exo -Fe(CO)3 -complexed 5,6-dimethylidene-2-bicyclo-[2.2.2]octanone 7 and 8. NaBH4 reduction of exo-complexes 7 gives a mixture of 3 and isomeric exo-alcohol 18, whereas reduction of endo-complexes 8 gives the endo-alcohol, endo-complexes 19, as the sole product. The base-catalyzed H/D exchange of 7 and 8 afford the dideuterated exo-complex 35 and the monodeuterated endo-complex 32, respectively. Oxidative hydroborations of the exo-(9) and endo-Fe(CO)3 (10) complexes of 5,6-dimethylidenebicyclo[2.2.1]hept-2-ene give the corresponding exo-alcohols 39 and 40. Oxidation of 39 and 40 gives the exo- and endo-complexes 41 and 42, respectively, of 5,6-dimethylidene-2-bicyclo[2.2.]heptanone. Only Hexo —C(3) can be exchanged in 42, wheres both H-atoms at C(3) in 41 are exchangeable. The endo-Fe(CO)3 group in 8 and 42 blocks the base-catalyzed H/D exchange of Hendo —C(3), thus providing a test for the configuration of Fe(CO)3 group in these systems. These studies have led to a revision of the iron configurations proposed by Hansen et al, [2] for 1, 2, 9 and 10.
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  • 74
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    Helvetica Chimica Acta 67 (1984), S. 361-364 
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    Keywords: Chemistry ; Organic Chemistry
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  • 75
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solvolysis rate constants in MeOH and t-BuOh are compared for β-methyl and β-phenyl derivatives of two cycloakyl systems. It appears that the β-phenyl derivatives solvolyse at te same rate as the β-methyl ones. The lack of deceleration is attributed to phenyl assistance. It is established by configurational analysis of the reaction products, that those products which necessarily originate from a cationic species are the most abundant ones. It is suggested that these reactions could proceed through ion-pair intermediates, which are nucleophilically solvated by phelyl or by the solvent. A parallel between phenyl assistance and ‘SN2 (intermediate)’ mechanism, suggested by Bentely & Schleyer, is drawn.
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  • 76
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    Helvetica Chimica Acta 67 (1984), S. 361-372 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The temperature dependence of the water self-diffusion coefficients (D), as well as those of low- and high-field (stationary and time-dependent) specific conductivities (K), have been determined in the percolation regime of ternary mixtures of water, AOT, and oil. For the first time a pronounced similarity in the behavior of D and κ was detected giving instructive hints about the large variations in the specific conductivities of these systems. Results from kinetic and stationary experiments are consistent with a network-structure model of micro phases in the percolation regime in which the micro phases retain their discrete character.
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  • 77
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    Topics: Chemistry and Pharmacology
    Notes: Facile synthesis of derivatives of 2,4-diphenyl-3-azabicyclo[3.3.1]nonane and 7,9-diphenyl-8-azabicyclo[4.3.1]decaneThe facile synthesis of hydantoins, cyanhydrins and aminonitriles derived from 2,4-diphenyl-3-azabicyclo[3.3.1]nonanone and 7,9-diphenyl-8-azabicyclo[4.3.1]decanone is described. Configurations at C(9) or C(10) of the new compounds wth pharmaceutical and synthetical utility is deduced from their spectral properties.
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  • 78
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    Helvetica Chimica Acta 67 (1984), S. 1328-1347 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the D-arabino- and D-ribo-ortholactones 13a-f and 15b-f and their treatment with Zn leading to the unsaturated esters 14a-d and 16a-d are described. Possible fragmentation mechanisms are discussed. The results were only compatible wit a concerted, nonsynchronous process, where both the axial lone pair of the ring oxygen atom and the lone pair formed during rupture of the C(5), O-bond participate in the elimination of the axial and of the equatorial C(1)-alkoxy groups, respectively.
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  • 79
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    Helvetica Chimica Acta 67 (1984), S. 1368-1373 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This communication reports ESR-spectroscopic investigations of the radical anion of 1,8-dimethyl[14]annulene (1) which possesses a flexible molecular framework allowing configurational and conformational mobility. The ESR and ENDOR spectra indicate that at higher temperatures (T 〉 160 K), \documentclass{article}\pagestyle{empty}\begin{document}$ 1^{- \atop \dot{}} $\end{document} exists as a mixture of several distinct isomers. One of them, the sole product at T 〈 160 K, is found to be energetically preferred. The configuration and the conformation of this species can be determined by interpretation of the hyperfine data in terms of a singly occupied MO of the 14-membered π-perimeter.
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  • 80
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    Helvetica Chimica Acta 67 (1984), S. 1386-1396 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-(tert-Butyl)-3,7-dehydrotropone (7-(tert-butyl)bicyclo[3.2.0]hepta-1(7),2,4-trien-6-one; 1) was found to dimerize reversibly to 2A by [2 + 4]-cycloaddition/cycloreversion reaction. The equilibrium lies on the side of the highly strained dimer 2A in the solid state, and on the side of the monomer 1 in solution. The [2 + 4]-reaction is fully perisite-, regio- and stereoselective. Above room temperature, 1 irreversibly formed a decarbonylated dimer 6, probably via the intermediate 9A or 9B, which resulted either from a dimerisation of 1 by [4 + 6]-cycloaddition or from a sigmatropic rearrangement of the originally formed dimer 2A or 2B. Similary, the 6-bromo derivative 14 afforded the corresponding decarbonylated dimer 15. Should the formation of 6 and 15 be due to a primary cycloaddition then that reaction is fully peri-, site- and regioselective. Mild LiAlH4-reduction of 6 and subsequent acetylation yielded the acetate 11, the structure of which was established by an X-ray analysis. More vigorous LiAlH4-treatment also reduced the terminal fulvenoid double bond of 6 and acetylation of the crude product led to the acetated 12 and 13.
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    Helvetica Chimica Acta 67 (1984), S. 1427-1428 
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    Keywords: Chemistry ; Organic Chemistry
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    Helvetica Chimica Acta 67 (1984), S. 1427-1438 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electromotive Behaviour of Liquid-membrane Electrode Assemblies Based on Enantiomer-selective Chiral IonophoresA comprehensive theoretical treatment is given for the potentiometric behavior of enantiomer-selective membrane electrodes based on chiral ionophores and plasticizers. The membrane model allows for free and complexed enantiomeric or racemic ions (e.g. ephedronium and l-phenylethylammonium ions) as well as for achiral interfering ions. Experiments are derived for the determination of the stoichiometry and the relative stability of enantiomeric ion/enantiomeric ligand complexes, and for the analytical measurement of the enantiomeric excess of ions in solution.
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  • 83
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    Topics: Chemistry and Pharmacology
    Notes: Water exchange of square-planar Pd(H2O)24+ has been studied as a function of temperature (240 to 345 K) and pressure (0.1 to 260 MPa, at 324 K) by measuring the 17/O-FT-NMR line-widths of the resonance from coordinated water at 27.11 and 48.78 MHz. The following exchange parameters were obtained: k298ex = (560 ± 40) s-1, ΔH* = (49.5 ± 1.9) kJ mol-1, ΔS* = - (26 ± 6) J K-1 mol-1 and ΔV* = - (2.2 ± 0.2) cm3 mol-1. The values refere to an aqueous perchlorate medium with an ionic strength between 2.0 and 2.6 m and a perchloric-acid concentration between 0.8 and 1.7 m, and are interpreted in terms of an associative (a) activation for the exchange. The exchange rate for Pd(H2O)24+ is 1.4 × 106 times faster than for Pt(H2O)24+ at 298 K. A comparison with reactions between other nucleophiles and Pd(H2O)24+ is also made.
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  • 84
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    Keywords: Chemistry ; Organic Chemistry
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    Topics: Chemistry and Pharmacology
    Notes: Studies of Organometallic Compounds, XX. Selectivity of 1,4-Addition of Benzyltitanium Compounds with BenzylildenacetoneTetrabenzyltitanium and dialkoxydibenzyltitanium compounds give essentially 1,4- addition with trans-4-phenyl-3-buten-2-one.
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  • 85
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    Topics: Chemistry and Pharmacology
    Notes: Aminative Reductive Coupling of Aromatic Aldehydes to N,N,N′,N′-Tetraalkyl-1,2-diarylethylenediamines, Induced by Tris(dialkylamino)methylvanadium (IV)In a novel type of reaction, certain aromatic aldehydes (benzaldehyde, p-methoxybenzaldehyde, 1-naphthaldehyde, furan-2-carbaldehyde) and secondary amines are coupled to give N,N,N′,N′-tetraalkyl-1,2-diarylethylenediamines 1-6. The reagents are tris(dialkylamino)methylvanadium(IV) compounds (cf. Eqn. 2). These are generated in situ either from isolable chlorotris(dialkylamino) vanadium(IV) (Eqn. 3), or preferably, from an Et2O/pentane solution of VCl4 which is treated sequentially with 3 equiv. of lithium dialkylamide, 1 equiv. of MeLi, and 0.8 equiv. of an aromatic aldehyde, to give the products 1-6 in a one-pot preparation (Scheme 2). The yields range from 14 to 54%. The diastereoisomeric mixtures (meso- and (±)-forms) obtained are separated by chromatography (Al2O3, petroleum ether/Et2O/Et3N), and the pure stereoisomers fully characterized. A mechanism of the reductive coupling induced by CH3V (NR2)3 is proposed (Scheme 1).
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    Helvetica Chimica Acta 67 (1984), S. 1506-1514 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several oxidative, reductive and C,C-cleavage reactions were performed starting from the three bicyclo[4.2.1]nona-3,7-diene-2-one derivatives 1, 5 and 18. The oxidations were selective and led to the diols 2,8 and 9, and the epoxides 6,9, and 20. The reductions were selective only in the case of 20 21; otherwise they led to mixtures of the alcohols 10 and 11, and of the dienes 14 and 15. The periodate ring cleavages afforded the functionalized cycloheptane derivatives 3, 12, 13 and 16. Configurational assignments were made on the basis of detailed 1H-NMR and X-ray analysis of 20.
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    Helvetica Chimica Acta 67 (1984), S. 1531-1534 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Red-Coloured Abietanoids from Leaf-Glands of Plectranthus strigosus BENTH.Chromatographic examination of the red-coloured diterpenoids from the South-African title plant yielded the following compounds: parviflorone A(1), parviflorone B (2), parviflorone C(3), parviflorone E (4) parviflorone D (5), parviflorone F (6), parviflorone G (7), and parviflorone H (8). Compounds 7 and 8 represent new variants of these quinone methides.
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  • 88
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    Notes: Polar Diterpenoids from Leaf-Glands of Plectranthus argentatus S. T. BLAKEFrom the red leaf-glands of the Australian Plectranthus argentatus the following novel diterpenoids were isolated: coleon-U-quinone (1), 8α,9α-epoxycoleon-U-quinone (3), 6β-formyloxy-7α-hydroxyroyleanone (7), and 5,6-dihydrocoleon U (10), besides the already known compounds 6β, 7α-dihydroxyroyleanone (4), 7α-acetoxy-6β-hydroxyroyleanone (5), and 7α-formyloxy-6β-hydroxyroyleanone (6). Epoxydation of 1 by perborate led in 32% yield to the epoxyquinone 3.
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    Helvetica Chimica Acta 67 (1984), S. 1568-1571 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Partially protected 4- or 5-hydroxy-sugar oximes were transformed into 5- or 6-membered 1-C-nitroglycosyl chlorides, respectively, by reaction with NaOCl under phase-transfer conditions. With the exception of the oxidation of the gluco-derivative 1 giving the anomers 6 and 7, the reactions were completely diastereoselective.
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  • 90
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    Helvetica Chimica Acta 67 (1984), S. 1572-1579 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and the liquid-crystal temperatures of sixty 4-cyano-2-fluorophenyl and 4-cyano-3-fluorophylen 4-substituted benzoates are described. The nematic-isotropic liquid transition temperatures of the most of these novel esters are only marginally lower than those of the corresponding esters containing an H-atom in place of the F-substituent. In several instances, the clearing points of the F-substiuted-phenyl esters are higher than those of the non-substituted-phenyl esters. The nematic ranges of several of the new esters are markedly broader than those of the analogous non-F-substituted-phenyl esters.
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  • 91
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    Helvetica Chimica Acta 67 (1984), S. 1588-1592 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H-NMR and vapor-pressure osmometry results are presented, which indicate the occurrence of a rapid equilibrium involving the head-to-head dimerization of β44-helices in chloroform solutions of HCO-L-Ile-(D-AIle-L-Ile)4-OMe. This equilibrium typifies the one that, in Urry's view, would be responsible for the formation and breaking down of the ion-conducting channels formed by gramicidin A in lipid bilayers.
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  • 92
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    Topics: Chemistry and Pharmacology
    Notes: The synthesis and liquid-crystal transition temperatures of forty ester derivatives of 2-fluoro-4-hydroxybenzonitrile and 3-fluoro-4-hydroxybenzonitrile are reported. The esters contain the trans-1,4-disubstituted cyclohexane or the 1,4-disubstituted bicyclo[2.2.2]octane rings (some contain an additional phenyl ring). Many of the novel F-substituted esters exhibit substantially higher nematic-isotropic transition temperatures than the corresponding unsubstituted esters. The order of clearing points of these laterally substiuted esters differing only in the presence of a benzene ring and the above-mentioned rings id established.
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  • 93
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    Helvetica Chimica Acta 67 (1984), S. 1598-1602 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of New Morphine Partial Structure 15,16-SecomorphinanThe synthesis of a new morphine partial structure, 15,16-secomorphinan, is described. One of the series, (±)-15, 16-secocyclorphan (5), has the analgesic potency of morphine and exhibits good binding to the opiate receptor.
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  • 94
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diastereoselective Synthesis of Novel Mannich (Bases1) through Titanium ReagentsTrichlorotitanium dialkylamino-alkoxides (2; titanates of N, O-hemiacetals) are generated either from the corresponding lithium alkoxides and titanium tetrachloride (Scheme 1) or by addition of trichloro-dialkuylamino-titanium to aldehydes. The electrophilic (dialkylamino) alkylating reagents 2 are used to convert lithium enolates to β-dialkylamino-ketones and -esters 5 (Mannich bases), see Scheme 2 and Table. One diastereoisomer of the products 5g-5p thus obtained with cyclohexenolate is formed preferentially (66-84%). The configuration of the products of this first diastereoselective version of the Mannich reaction could not yet be determined. A typical procedure for carrying out the reaction is given.
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  • 95
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 67 (1984), S. 1612-1615 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new, practical method for the optical resolution of bicyclic ketones if illusttrated by the preparation of (+)-(1R,4R)-7-oxabicyclo[2.2.1]bept-5-en-2-one ((+)-1) and (+)-(1R, 2S,4R)-2-cyano-7-oxabicyclo[2.2.1]hept-5-en-2-yul acetate ((+)-4). It involves the diastereoselective formation of a brucine complex with the corresponding cyanhydrine mixture.
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  • 96
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of three-coordinate bis(dialkylphosphinomethyl)benzo[c]phenanthrene Ag(I) complexes, alkyl= t-Bu, (1b), and cyclohexyl, (1c), anion = BF4, CIO4, CIO4, NO3, Cl, Br, I, have been prepared and thier 31P-NMR characteristics recorded. The solid state structures of [Ag(1b)Br], [Ag(1b)Cl] and [Ag(1b)CIO4] have been determined by X-ray diffraction. The Ag atom in these complexes shows distorted trigonal geometry. Selected bond lengths and angles are as follows: Ag-P = 2.463(4) Å and 2.433(5) Å, P-Ag-P=141.6(2)° in the bromo complex, Ag-P = 2.457(2) Å and 2.427(2) Å, P-Ag-P = 142.6(1)° ion the chloro complex, and Ag-P = 2.394(2) and 2.393 (2) Å, P-AG-P = 161.5(1)° in the perchlorato complex.
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  • 97
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 67 (1984), S. 1625-1629 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two new syntheses of verrucarinic acid (2S, 3R-dihydroxy-3-methylpentanoic acid) and its derivatives, suitably protected for the further conversion to macrocyclic trichothecenes, are described. The first one makes use of a diastereoselective alkylation of a (-)-(S)-malic acid ester and the regioselective reductin of one carboxyl function toa methyl group. The second approach involves a stereoselective addition of an allylsilane to a chiral glyoxylate.
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  • 98
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Control of the Catalytic Synthesis of Pyridine from Alkynes and Nitriles by the (η6-Borinato)-Nigands at Cobaltη6-Borinato groups as ligands at cobalt have unique effects on the chemo- and negioselectivity of the catalytic co-cyclization of alkynes and nitriles. The turnover number of the conversion of acrylonitrile and acetylene to give 2-vinylpyridine is considerably enhanced. Cyano compounds wih polar substitutents such as amino or thio groups can also be reacted. The homogeneous reaction of HCN with acetylene giving pyridine has been achieved for the first time.
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  • 99
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The endocyclic double bond C(2), C(3) in 5,6-dimethylidene-7-oxabicyclo[2.2.1]-hept-2-ene (1) can he coordinated selectively on its exo-face before complexation of the exocyclic s-cis-butadiene moiety. Irradiation of Ru3(CO)12 or Os3(CO)12 in the presence of 1 gave tetracarbonyl [(1R,2R, 3S,4S)-2,3-η-(5,6-dimethylidene-7-oxabicyclo[2.2.1]-hept-2-ene)]ruthenium (6) or -osmium (8). Similarly, irradiation of Cr(CO)6 or W(CO)6 in the presence of 1 gave pentacarbonyl[(1R, 2R, 3S,4S)-2,3-η-(5,6-dimethylidene-7-oxabicyclo[2.2.1]hept-2-ene)]chromium (10) or -tungsten (11). Irradiation of complexes 6 and 11 in the presence of 1 led to further CO substitution giving bed-tricarbonyl-ae-bis[(1R,2R,3S,4S)-2,3-η-(5,6-dimethylidene-7-oxabicyclo[2.2.1]hept-2-ene)]ruthenium (7) and trans-tetracarbonyl[(1R,2R,3S,4S)-2,3-η-(5,6-dimethylidene-7-oxabicyclo-[2.2.1]hept-2-ene)]tungsten (12), respectively. The diosmacyclobutane derivative cis-m̈-[(1R,3R,3S,4S)-(5,6-dimethylidene-7-oxabicyclo[2.2.1]hepta-2,3-diyl)]bis(tetracarbonyl-osmium) (Os-Os) (9) wa also obtained. The Diels-Alder reactivity of the exocyclic s-cis-butadiene moiety in complexs 7 and 8 was found to be significantly higher than that of the free triene 1.
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  • 100
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The products generated by heating 5,6-dimethylidene-7-oxabicyclo[2.2.1]hept-2-ene (1) with Fe2(CO)9, Ru3(CO)12, Os3(CO)12, Cr(CO)3(MeCN)3, (or W(CO)5(MeCN) or by treatment with Fe-atoms have been characterized by spectroscopic methods. Apart from the expected η2- and η4-complexes of the triene 1, condensation products are formed which arise from the formal [4 + 2]-cyclodimerization of 1 involving the endocyclic double bond of one molecule and the diene moiety of a second. The [4 + 2]-cyclodimerization is catalyzed by Os3(CO)12 in MeOH and gives 1,4-epoxy-7-methoxy-2,3-dimethylidene-1,2,3,4,4a,9,9a,10-octahydroanthracene (15)). Fe-Atoms induce a stereoselective [2 + 2]-cyclodimerization pf 1 which involves its endocyclic double bond and produces the dimer 8.
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