Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs

Chirality. 2019 Jan;31(1):79-86. doi: 10.1002/chir.23038. Epub 2018 Dec 6.

Abstract

Enantioselective vinylation of aldehydes via direct catalytic asymmetric Grignard reaction of aldehdyes and the vinyl Grinard reagent is a long-standing challenge. This work demonstrated that the magnesium (S)-3,3'-dimethyl BINOLate enantioselectively catalyze the direct vinylation of aldehydes with the deactivated vinylmagnesium bromide by bis(2-[N,N'-dimethylamino]ethyl) ether (BDMAEE) in the addition of n-butylmagnesium chloride. The highest ee of 63% was achieved up to date.

Keywords: BINOL; Grignard reaction; asymmetric catalysis; deactivation; vinylation.

Publication types

  • Research Support, Non-U.S. Gov't