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  • Articles  (80)
  • Articles: DFG German National Licenses  (80)
  • 2010-2014
  • 1980-1984  (9)
  • 1955-1959  (69)
  • 1940-1944  (2)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 12 (1940), S. 120-120 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 71 (1958), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 113 (1982), S. 237-263 
    ISSN: 1434-4475
    Keywords: Polymerization kinetics ; Quasiequilibrium ; RNA-replication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Ein vereinfachter Mechanismus derRNA-Replikation durch eine spezifische Polymerase wird durch direkte numerische Integration und mit Hilfe der Annahme von „Quasigleichgewicht“ analysiert. Die Quasigleichgewichtsannahme wird an Hand von drei Beispielen einfacher Zweistufenreaktionen mathematisch definiert. Die drei Beispiele beschreiben: (1) die Annäherung an den Gleichgewichtszustand, (2) den irreversiblen Abbau und (3) das unbeschränkte Wachstum einer Verbindung.
    Notes: Abstract A simplified mechanism ofRNA-replication by a specific polymerase is analysed by direct numerical integration and by means of the “quasiequilibrium approximation”. The quasiequilibrium approximation is formulated in precise mathematical terms for three simple, two step reactions which describe approach towards equilibrium, irreversible transformation and unlimited growth.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 122 (1941), S. 212-213 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 1506-1519 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Acylation Reactions of Carbonyl Compounds with 1-Acylpyridinium Salts1-Acyl-4-benzylpyridinium tetrafluoroborates 5 have been used to derive generally applicable guidelines for the reaction of aldehydes 6 and ketones 7 with 1-acylpyridinium salts (scheme 2): a) Non-enolizable aldehydes 6 react with 5 to give N-[1-(aryl- or alkylcarbonyloxy)alkyl]pyridinium salts 14. b) Enolizable aldehydes 6 can be transformed by means of 5 into pyridinium salts 14 and enol esters 12, respectively. Using aldehyde 6b as an example, it was possible to show that the reaction course (formation of 12 or 14) can be controlled by simple variation of the reaction conditions. c) In general, ketones will not react with 5. The range of applicability of this guidelines has been defined. - We suggest, that the reaction course is mainly determined by the formation of the carbenium ion 19 and the aldehyde-pyridine derivative addition product 8.
    Notes: Durch die Verwendung von 1-Acyl-4-benzylpyridinium-tetrafluoroboraten 5 werden allgemein-gültige Aussagen über die Reaktionsmöglichkeiten von Aldehyden 6 und Ketonen 7 mit 1-Acylpyridiniumsalzen gewonnen (Schema 2): a) Nicht-enolisierbare Aldehyde 6 reagieren mit 5 zu N-[1-(Aryl- bzw. Alkylcarbonyloxy)alkyl]pyridiniumsalzen 14, b) enolisierbare Aldehyde 6 können mittels 5 sowohl in die Pyridiniumsalze 14 als auch in Enolester 12 übergeführt werden, der Reaktionsverlauf ist - wie vor allem am Beispiel des Aldehyds 6b gezeigt wird - bezüglich der Reaktionsverlauf ist - wie vor allem am Beispiel des Aldehyds 6b gezeigt wird - bezüglich der Natur der Produkte (12 oder 14) durch einfache Variation der Reaktionsbedingungen lenkbar. c) Ketone reagieren i. a. nicht mit 5. Der Gültigkeitsbereich dieser Aussagen wird definiert. - Wir vermuten, daß der Reaktionsverlauf durch die Bildung des Carbenium-Ions 19 sowie eines aus Aldehyd und Pyridin-Derivat entstehenden Addukts 8 bestimmt wird.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 1034-1038 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [1-(Arylcarbonyloxy)alkyl]phosphonium Salts, 31). Reductive C-Acylation of Aromatic AldehydesThe phosphonium salts 5 are synthesized from aldehydes 1, arenecarbonyl chlorides 2 and triphenylphosphane (4), and can then be deprotonated to 7. 7 react as acyl anion equivalents with aromatic aldehydes 9 forming enol esters 10, which are transformed to alkanones 11. The new aldehyde 9 → alkanone 11-transformation is characterised as a reductive C-acylation of aromatic aldehydes.
    Notes: Aus Aldehyden 1, Arencarbonsäurechloriden 2 und Triphenylphosphan 4 entstehen die Phosphoniumsalze 5, die zu 7 deprotoniert werden. 7 reagiert wie Acylanionäquivalente mit aromatischen Aldehyden 9 zunächst zu Enolestern 10, aus denen die Alkanone 11 hergestellt werden. Die neuartige Aldehyd 9 → Keton 11-Umwandlung wird als reduktive C-Acylierung der Aldehyde 9 charakterisiert.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 155 (1957), S. 316-318 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 155 (1957), S. 274-275 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 155 (1957), S. 287-289 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 155 (1957), S. 297-297 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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