Issue 3, 1969

Nitroxide radicals. Part IV. The oxidation of cyclic N-hydroxy-imides

Abstract

Oxidation of N-hydroxy-naphthalimide and -phthalimide with lead tetra-acetate gave mainly products formed by coupling of the corresponding imidoxy-radicals with radicals derived from the solvent. Oxidations in methylene chloride yielded unsymmetrical dimeric products.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 512-516

Nitroxide radicals. Part IV. The oxidation of cyclic N-hydroxy-imides

A. Calder, A. R. Forrester and R. H. Thomson, J. Chem. Soc. C, 1969, 512 DOI: 10.1039/J39690000512

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