Issue 19, 1971

Conrotatory ring opening of cyanostilbene oxides to carbonyl ylides

Abstract

The structure of the cycloadducts from 2-cyano-trans-stilbene oxide with acetylenic and olefinic dipolarophiles confirm the electrocyclic C–C ring scission of the oxiran while the cycloadditions of 3 cyano-trans- and cis-stilbene oxide to dimethyl fumarate establish the conrotatory course.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1192-1194

Conrotatory ring opening of cyanostilbene oxides to carbonyl ylides

A. Dahmen, H. Hamberger, R. Huisgen and V. Markowski, J. Chem. Soc. D, 1971, 1192 DOI: 10.1039/C29710001192

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