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 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.2005.1124 |