Abstract

Abstract Reactions of (dimethylamino)phenylsulfoxonium methylide with triphenylvinylphosphonium salts gave the corresponding cyclopropyltriphenylphosphonium salts (E-form) in high yields, when 1,8-diazabicyclo[5.4.0]undec-7-ene was used as a base. Reactions of cyclopropyltriphenylphosphonium salts with sodium hydride in the presence of tris[2-(2-methoxyethoxy)ethyl]amine afforded the corresponding ylides, which further reacted with aldehydes to give alkylidenecyclopropanes in high yields.

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