Issue 18, 1990

Convergent synthesis of methylenomycin B via selenium-assisted intramolecular SN2′ cyclization

Abstract

A highly convergent and efficient synthesis of methylenomycin B has been achieved by the reaction of the lithium enolate of 4-chloro-4,5-dimethyl-5-hexen-3-one with phenylselenenyl bromide followed by selenoxide elimination.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1264-1266

Convergent synthesis of methylenomycin B via selenium-assisted intramolecular SN2′ cyclization

J. Mathew, J. Chem. Soc., Chem. Commun., 1990, 1264 DOI: 10.1039/C39900001264

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