Issue 4, 1990

Concurrent configurational modification in conjugated dienes; a new pathway in the isomerization of alkadienes

Abstract

The hexa-2,4-diene derivative (2), obtained from 1,6-di(phenylsulphonyl)hexa-2,4-diyne (1), is shown to undergo simultaneous Isomerization at both double bonds, through an elimination-addition pathway.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 328-330

Concurrent configurational modification in conjugated dienes; a new pathway in the isomerization of alkadienes

B. S. Thyagarajan and R. A. Chandler, J. Chem. Soc., Chem. Commun., 1990, 328 DOI: 10.1039/C39900000328

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