| Literature DB >> 30650228 |
Gregg M Schwarzwalder1, Carson D Matier1, Gregory C Fu1.
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.Entities:
Keywords: alkylation; asymmetric catalysis; cross-coupling; nickel; silicon
Year: 2019 PMID: 30650228 PMCID: PMC6399024 DOI: 10.1002/anie.201814208
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336