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  • Luciferin  (1)
  • Neighboring-group effects  (1)
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  • 1
    Digitale Medien
    Digitale Medien
    Chemiluminescence in Organic CompoundsDedicated to Professor Fritz Micheel on the occasion of his 65th birthday (1965)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 566-573 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Chemiluminescence ; Luminescence ; Phthalylhydrazides ; Luciferin ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: As a result of the development of very sensitive equipment, it is now possible to show that the chemiluminescence of organic compounds in solution is quite a common phenomenon. Notable advances have been made during recent years in the investigation of the chemiluminescence of substituted phthalic acid hydrazides and related compounds. A new and probably generally applicable method of producing chemiluminescence has recently been discovered in the reaction of aromatic free-radical anions with appropriate free-radical cations.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196505661
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Neighboring Group and Substituent Effects in Organosulfur Compounds (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 674-683 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Neighboring-group effects ; Substituent effects ; Organosulfur compounds ; Alkylthio groups ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Thioether groups participate in nucleophilic substitution reactions at adjacent carbon atoms, in the addition of alkane and arenesulfenyl halides onto olefinic double bonds, and in elimination reactions which lead to olefins and which proceed via intermediate episulfonium ions. Studies of alkylthioacrylic acid derivatives, which are readily synthetized because of the neighboring group effect, show that the presence of thioether groups in the α-position of acrylic acid systems leads to particularly high reactivity in “head-to-head” dimerizations.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196306741
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