Issue 16, 2023

Enantioselective copper-catalyzed hydrophosphination of alkenyl isoquinolines

Abstract

An enantioselective hydrophosphination of alkenyl isoquinolines is developed by using a copper-chiral diphosphine ligand catalyst. It provides a direct and atom-efficient approach to prepare a variety of chiral phosphines with an isoquinoline unit in good yields and high enantioselectivities. In addition, these chiral phosphine products are useful bidentate P,N-ligands which showed potential application in asymmetric catalysis.

Graphical abstract: Enantioselective copper-catalyzed hydrophosphination of alkenyl isoquinolines

Supplementary files

Article information

Article type
Edge Article
Submitted
19 Dec 2022
Accepted
20 Mar 2023
First published
21 Mar 2023
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., 2023,14, 4413-4417

Enantioselective copper-catalyzed hydrophosphination of alkenyl isoquinolines

Q. Yang, J. Zhou and J. (. Wang, Chem. Sci., 2023, 14, 4413 DOI: 10.1039/D2SC06950D

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