Enantioselective Hydroalkylation of α,β-Unsaturated Amides through Reversed syn-Hydrometallation of NiH

02 February 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Enantioselective synthesis of a wide range of structurally diverse β-chiral amides has been achieved through nickel-catalyzed regio-reversed hydroalkylation of α,β-unsaturated amides with alkyl iodides in the presence of a hydrosilane. Different from the classical homolysis/enantioconvergent recombination process of Ni(III) intermediates as the enantio-determining step, chiral induction in this reductive hydroalkylation was achieved through an enantiodifferentiating regio-reversed syn-hydrometallation process of α,β-unsaturated amides.

Keywords

Asymmetric catalysis
nickel
nickel hydride
hydroalkylation
regioselectivity
alkenes

Supplementary materials

Title
Description
Actions
Title
Zhou Reverse Hydroalkylation SI
Description
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