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Merck
CN

Enantioselective dichlorination of allylic alcohols.

Journal of the American Chemical Society (2011-05-06)
K C Nicolaou, Nicholas L Simmons, Yongcheng Ying, Philipp M Heretsch, Jason S Chen
ABSTRACT

The development of an enantioselective allylic alcohol dichlorination catalyzed by dimeric cinchona alkaloid derivatives and employing aryl iododichlorides as chlorine sources is reported. Reaction optimization, exploration of the substrate scope, and a model for stereoinduction are presented.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Cinnamyl alcohol, 98%
Sigma-Aldrich
Cinnamyl alcohol, ≥98%, FG