Issue 11, 1981

The role of cyclohexadienones in the thermal sigmatropic rearrangements of 2-oxidoanilinium ylides

Abstract

Thermal isomerisation of N-allyl-2-oxidoani-linium ylides under mild conditions yields three products which are each formed by two types of competitive pathways; the minor pathway involves a radical pair intermediate and three modes of coupling, and the major pathway involves a collection of concerted sigmatropic rearrangements.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 573-575

The role of cyclohexadienones in the thermal sigmatropic rearrangements of 2-oxidoanilinium ylides

W. D. Ollis, R. Somanathan and I. O. Sutherland, J. Chem. Soc., Chem. Commun., 1981, 573 DOI: 10.1039/C39810000573

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