Issue 18, 1972

On the stereoselectivity of the electrocyclic process, benzocyclobutene to o-quinone dimethide

Abstract

Benzocyclobutene derivatives bearing an oxygen substituent at position 1 undergo conrotatory thermal ring opening to yield reactive diene species in which the oxygen substituent preferentially adopts the (E)-configuration.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1034-1035

On the stereoselectivity of the electrocyclic process, benzocyclobutene to o-quinone dimethide

B. J. Arnold and P. G. Sammes, J. Chem. Soc., Chem. Commun., 1972, 1034 DOI: 10.1039/C39720001034

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