Enantioconvergent Cross-Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes

Angew Chem Int Ed Engl. 2019 Mar 11;58(11):3571-3574. doi: 10.1002/anie.201814208. Epub 2019 Feb 6.

Abstract

Metal-catalyzed enantioconvergent cross-coupling reactions of alkyl electrophiles are emerging as a powerful tool in asymmetric synthesis. To date, high enantioselectivity has been limited to couplings of electrophiles that bear a directing group or a proximal p/π orbital. Herein, we demonstrate for the first time that enantioconvergent cross-couplings can be achieved with electrophiles that lack such features; specifically, we establish that a chiral nickel catalyst can accomplish Negishi reactions of racemic α-halosilanes with alkylzinc reagents with good enantioselectivity under simple and mild conditions, thereby providing access to enantioenriched organosilanes, an important class of target molecules.

Keywords: alkylation; asymmetric catalysis; cross-coupling; nickel; silicon.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkylation
  • Catalysis
  • Coordination Complexes / chemistry*
  • Molecular Structure
  • Nickel / chemistry*
  • Organosilicon Compounds / chemical synthesis*
  • Stereoisomerism
  • Zinc Compounds / chemistry

Substances

  • Coordination Complexes
  • Organosilicon Compounds
  • Zinc Compounds
  • Nickel