Issue 0, 1974

Stable free radicals. Part II. Some substituted pyridinyls

Abstract

Cyano and methoxycarbonyl substituents at the 2- and 6-positions, unlike methyl groups, strongly stabilize pyridinyl radicals, particularly if the 4-position is blocked. The structure–stability relationships in this series afford further evidence for the zwitterionic stabilization of radicals.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 1427-1432

Stable free radicals. Part II. Some substituted pyridinyls

A. R. Katritzky and F. Soti, J. Chem. Soc., Perkin Trans. 1, 1974, 1427 DOI: 10.1039/P19740001427

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