Issue 20, 1985

Formation of thiochromans by cycloaddition reactions of the enethione resulting from thermal ring-cleavage fragmentation of 2-azidobenzo[b]thiophene with olefins

Abstract

The enethione arising from thermal ring-cleavage fragmentation of 2-azidobenzo [b]thiophene reacts with open chain and cyclic dienophiles to give thiochromans in fairly good yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1441-1443

Formation of thiochromans by cycloaddition reactions of the enethione resulting from thermal ring-cleavage fragmentation of 2-azidobenzo[b]thiophene with olefins

P. Spagnolo and P. Zanirato, J. Chem. Soc., Chem. Commun., 1985, 1441 DOI: 10.1039/C39850001441

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