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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 81 (1969), S. 321-328 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In wasserfreiem Fluorwasserstoff lassen sich an Verbindungen mit CC-Doppelbindungen in einem Schritt Fluor und ein anderer Substituent anlagern. Auf diese Weise sind u. a. α-fluorierte β-Halogen-, β-Alkyl-, β-Nitro- und β-Aminoverbindungen zugänglich, aber auch  -  teilweise durch Sekundärreaktionen  -  fluorierte Äther, Alkohole, Ester und Carbonsäuren. Durch konjugierte „Hypofluorierung“ in Gegenwart von Oxeniumionen können β-Fluoralkohole erhalten werden.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 8 (1969), S. 349-356 
    ISSN: 0570-0833
    Keywords: Hydrogen fluoride ; Solvents ; Fluorination ; Fluorine ; Addition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fluorine and another substituent can be added in a single step to compounds having CC double bonds in anhydrous hydrogen fluoride. It is possible in this way to obtain e.g. α-fluorinated β-halogeno, β-alkyl, β-nitro, and β-amino compounds, and also (in some cases by secondary reactions) fluorinated ethers, alcohols, esters, and carboxylic acids, β-fluoro alcohols can be obtained by conjugated “hypofluorination” in the presence of oxenium ions.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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