NiH-Catalyzed Asymmetric Hydroarylation of N-Acyl Enamines: Practical Access to Chiral Benzylamines

14 October 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The enantio- and regioselective reductive hydroarylation of N-acyl enamines has been achieved with a NiH catalyst and a chiral bis-imidazoline ligand. A broad range of structurally diverse, enantioenriched benzylamines, a moiety found in many pharmacologically active molecules, have been synthesized efficiently under mild, operationally simple reaction conditions.

Keywords

alkenes
asymmetric ccatalysis
hydroarylation
nickel
regioselectivity

Supplementary materials

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Title
Asymmetric Hydroarylation of N-Acyl Enamine SI
Description
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