Enantioselective addition of a chiral thiazolidinethione-derived titanium enolate to acetals

Org Lett. 2001 Feb 22;3(4):615-7. doi: 10.1021/ol0070177.

Abstract

[reaction: see text] High stereoselectivities (up to 98% de) have been achieved for the Lewis acid-mediated cross-coupling reaction of dimethyl acetals to a chiral 1,3-thiazolidine-2-thione-derived titanium enolate. The reaction affords enantiopure anti alpha-methyl-beta-alkoxy carbonyl compounds in a wide range of acetals.