Selective Synthesis of Isocyanides from Secondary Alcohols by a New Type of Oxidation–Reduction Condensation

Selective synthesis of isocyanides from secondary alcohols via alkyl diphenylphosphinites is established by a new type of oxidation–reduction condensation in controlling the ambident reactivity of cyanide anion. In the presence of ZnO, isocyanides are obtained exclusively in moderate to high yields....

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Veröffentlicht in:Chemistry letters 2005-08, Vol.34 (8), p.1124-1125
Hauptverfasser: Masutani, Kouta, Minowa, Tomofumi, Mukaiyama, Teruaki
Format: Artikel
Sprache:eng
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Zusammenfassung:Selective synthesis of isocyanides from secondary alcohols via alkyl diphenylphosphinites is established by a new type of oxidation–reduction condensation in controlling the ambident reactivity of cyanide anion. In the presence of ZnO, isocyanides are obtained exclusively in moderate to high yields.
ISSN:0366-7022
1348-0715
DOI:10.1246/cl.2005.1124