Mono- and Di-2,2,2-Trichloroethyl Acetals as Protecting Groups

Document Type

Article

Publication Date

2-1-1973

Abstract

Mono- and di-2,2,2-trichloroethyl acetals have been selectively prepared in good yields by acid-catalyzed alcohol exchange with 2,2,2-trichloroethanol and dimethyl or diethyl acetals. A nonacidic and aprotic reductive cleavage using activated zinc dust in ethyl acetate or THE regenerates the carbonyl.

DOI

10.1021/jo00943a030

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