Accéder au contenu
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
RÉSUMÉ

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].

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
(S)-4-Benzyl-2-oxazolidinone, 99%