Issue 23, 2024

Ir/XuPhos-catalyzed direct asymmetric reductive amination of ketones with secondary amines

Abstract

A diverse array of bidentate P-containing ligands has been developed for Ir-catalyzed asymmetric hydrogenation, but chiral monodentate phosphine ligands have remained comparatively underexplored. We herein report a novel iridium catalyst with XuPhos as a chiral monodentate phosphine ligand for the direct asymmetric reductive amination of ketones with secondary amines. This catalytic system tolerates a wide range of substrates, providing a series of chiral tertiary amines efficiently with high enantioselectivities. The high catalytic activity is attributed to the presence of the aliphatic cyclohexyl group on the P-atom and the relative configuration of the ligand, which is crucial for XuPhos to act as a monodentate P-ligand for iridium.

Graphical abstract: Ir/XuPhos-catalyzed direct asymmetric reductive amination of ketones with secondary amines

Supplementary files

Article information

Article type
Research Article
Submitted
14 Aug 2024
Accepted
29 Sep 2024
First published
05 Oct 2024

Org. Chem. Front., 2024,11, 6735-6741

Ir/XuPhos-catalyzed direct asymmetric reductive amination of ketones with secondary amines

Z. Luo, T. Fan, J. Luo, Y. Liu and J. Zhang, Org. Chem. Front., 2024, 11, 6735 DOI: 10.1039/D4QO01495B

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