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An efficient synthesis of C2-symmetric chiral binaphthyl ketone catalysts
T Furutani1, M Hatsuda, T Shimizu
1Product & Technology Development Laboratory, Tanabe Seiyaku Co. Ltd., Osaka, Japan.
Bioscience, Biotechnology, and Biochemistry
|March 29, 2001
Abstract:
An efficient synthesis of C2-symmetric chiral binaphthyl ketones 1a and b, effective catalysts for asymmetric epoxidation, is reported. The key features of this synthesis are Co(salen)-catalyzed macrolactonization of racemic 1,1'-binaphthyl-2,2'-dicarboxylic acid monoglycidyl esters 3a and b and lipase-catalyzed enantioselective acylation of resulting 11-membered cyclic binaphthyl alcohols 4a and b.