Issue 8, 1970

Mode of action of carcinogenic amines. Part I. Oxidation of N-arylhydroxamic acids

Abstract

Oxidation of N-arylhydroxamic acids in benzene with silver oxide gave the corresponding aryl nitroso-compounds, NO-diacylarylhydroxylamines, aryl nitro-compounds, and amides. The first two types of product are considered to arise by an intermolecular electrophilic acylation reaction and the other two by a homolytic oxygen-transfer process.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1081-1083

Mode of action of carcinogenic amines. Part I. Oxidation of N-arylhydroxamic acids

A. R. Forrester, M. M. Ogilvy and R. H. Thomson, J. Chem. Soc. C, 1970, 1081 DOI: 10.1039/J39700001081

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