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Original Articles

A Convenient Synthesis of Phenyl 1-Chloro-1 Alkenyl Chalcogenides by One-Pot Wittig Reaction. Synthesis of Selenolesters

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Pages 173-179 | Published online: 04 Oct 2006
 

Abstract

The preparation of 1-chloro-1-chalcogeno(sulfur, selenium) alkenes by a Wittig-type reaction in an one pot procedure is described. Chlorochalcogenyl triphenylphosphoranes are formed in situ by the reaction of dichloromethyl phenylchalcogenide, potassium t-butoxide and triphenylphosphine. They react with aldehydes to give 1-chlorovinyl chalcogenides as a mixture of isomers.

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