Issue 5, 2022

Manganese(i)-catalyzed access to 1,2-bisphosphine ligands

Abstract

Chiral bisphosphine ligands are of key importance in transition-metal-catalyzed asymmetric synthesis of optically active products. However, the transition metals typically used are scarce and expensive noble metals, while the synthetic routes to access chiral phosphine ligands are cumbersome and lengthy. To make homogeneous catalysis more sustainable, progress must be made on both fronts. Herein, we present the first catalytic asymmetric hydrophosphination of α,β-unsaturated phosphine oxides in the presence of a chiral complex of earth-abundant manganese(I). This catalytic system offers a short two-step, one-pot synthetic sequence to easily accessible and structurally tunable chiral 1,2-bisphosphines in high yields and enantiomeric excess. The resulting bidentate phosphine ligands were successfully used in asymmetric catalysis as part of earth-abundant metal based organometallic catalysts.

Graphical abstract: Manganese(i)-catalyzed access to 1,2-bisphosphine ligands

Supplementary files

Article information

Article type
Edge Article
Submitted
30 Nov 2021
Accepted
12 Jan 2022
First published
13 Jan 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2022,13, 1307-1312

Manganese(I)-catalyzed access to 1,2-bisphosphine ligands

L. Ge and S. R. Harutyunyan, Chem. Sci., 2022, 13, 1307 DOI: 10.1039/D1SC06694C

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