Issue 0, 1968

The action of toluene-p-sulphonyl azide on cyclic azomethines

Abstract

Toluene-p-sulphonyl azide gives cyclic amidines with 2-methyl-1-piperideine and 2,5-dimethyl-1-pyrroline. The products are rationalised on the basis of an imine–enamine equilibrium in the starting azomethines.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 227-228

The action of toluene-p-sulphonyl azide on cyclic azomethines

A. C. Ritchie and M. Rosenberger, J. Chem. Soc. C, 1968, 227 DOI: 10.1039/J39680000227

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