Issue 19, 1971

Cycloadditions of 1,2,3-triphenylaziridine via the azomethine ylide

Abstract

The pyrrolidine derivatives, which were obtained from 1,2,3-triphenylaziridine (configuration unknown) and dialkyl fumarate, dialkyl maleate, or trans-dibenzolyethylene, possess 2,5-trans-phenyl groups; the trans-substituted azomethine ylide must be the intermediate which undergoes the 1,3-dipolar cycloaddition.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1187-1188

Cycloadditions of 1,2,3-triphenylaziridine via the azomethine ylide

J. H. Hall and R. Huisgen, J. Chem. Soc. D, 1971, 1187 DOI: 10.1039/C29710001187

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