Enolization of chiral alpha-silyloxy ketones with dicyclohexylchloroborane. Application to stereoselective aldol reactions

Org Lett. 2000 Aug 24;2(17):2599-602. doi: 10.1021/ol006109t.

Abstract

[reaction: see text]Comprehensive analysis of the enolization of alpha-silyloxyketones by Chx2BCl/R3N has allowed us to design stereoselective Chx2BCl-mediated aldol processes that afford syn or anti aldol products and to disclose a hypothesis that accounts for the subtle effects that determine their enolization.