The reaction of ketene silyl acetals and silyl enol ethers with CCl₄ without a promoter

Abstract

The reaction of CCl₄ with ketene silyl acetals and silyl enol ethers in the absence of a promoter at ambient temperature or at reflux, or under photo-irradiation, was performed to form products via addition of the trichloromethyl group to those silyl substrates.

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