Issue 10, 1986

Cyano-O-silyhydroxylamines as nitrone blocking groups

Abstract

Addition of trimethylsilyl cyanide to N-alkyl-C-phenylnitrones affords cyano-O-silylhydroxylamines; reaction of these species with silver fluoride regenerates the nitrone in quantitative yield thereby providing a useful nitrone blocking group.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 789-790

Cyano-O-silyhydroxylamines as nitrone blocking groups

A. Padwa and K. F. Koehler, J. Chem. Soc., Chem. Commun., 1986, 789 DOI: 10.1039/C39860000789

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