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Merck

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
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Cinnamylalkohol, 98%
Sigma-Aldrich
Cinnamylalkohol, ≥98%, FG