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  • Articles: DFG German National Licenses  (2)
  • 1960-1964  (2)
  • 1890-1899
  • 1964  (2)
  • Free radicals  (2)
  • 1
    ISSN: 0570-0833
    Keywords: Free radicals ; Radical reactions ; Sulfur ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic free radicals of monovalent sulfur have not been hitherto observed in solution or in melts. Steric hindrance and resonance stabilization, which are responsible for the stability of the triarylmethyl, diphenylnitrogen, and phenoxyl radicals, are apparently insufficient to stabilize the organic free radicals of monovalent sulfur in such concentrations that they can be detected by current physical methods. - It was only in 1963 that aminopolysulfur radicals (R2N—Sn—S·) were detected in solution, and arylsulfur radicals (Ar-S·) and phenylselenium radicals were isolated at ca. -180°C. - Organically bound sulfur can be stabilized in the free-radical state if association of the radicals is prevented by fixing in a crystal lattice (“cystine radical”), by repulsion between radical ions (sulfinium salts), or by freezing-in (arylsulfur radicals).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 525-538 
    ISSN: 0570-0833
    Keywords: Radical reactions ; Free radicals ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the present article an attempt is made to summarize the steric requirements and the influence of neighboring groups which determine the course of intramolecular radical reactions. Steroids are used as substrates for these reactions, since here the spatial arrangement of the ring members and the distances between substituents are largely fixed. Furthermore, intramolecular free-radical reactions are of practical importance in steroid chemistry in connection with substitution at non-activated carbon atoms. Almost all the reactions discussed begin with the formation of an oxygen radical by oxidation of an alcohol with lead tetraacetate or by homolysis of the corresponding hypoiodite.
    Type of Medium: Electronic Resource
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