跳轉至內容
Merck

Total synthesis of (S)-equol.

Organic letters (2006-11-17)
Jennifer M Heemstra, Sean A Kerrigan, Daniel R Doerge, William G Helferich, William A Boulanger
摘要

The first enantioselective total synthesis of (S)-equol is reported. The described route relies on an Evans alkylation to form the stereocenter and an intramolecular Buchwald etherification to generate the chroman ring. Key features of this method include its brevity, its scalability, and the low cost of starting materials. [reaction: see text].

材料
產品編號
品牌
產品描述

Sigma-Aldrich
(S)-4-苄基-2-噁唑烷酮, 99%