Issue 14, 2021

Nickel-catalyzed asymmetric reductive arylation of α-chlorosulfones with aryl halides

Abstract

We report an asymmetric Ni-catalyzed reductive cross-coupling of aryl/heteroaryl halides with racemic α-chlorosulfones to afford enantioenriched sulfones. The reaction tolerates a variety of functional groups under mild reaction conditions, which complements the current methods. The utility of this work was demonstrated by facile late-stage functionalization of commercial drugs.

Graphical abstract: Nickel-catalyzed asymmetric reductive arylation of α-chlorosulfones with aryl halides

Supplementary files

Article information

Article type
Edge Article
Submitted
15 Jan 2021
Accepted
18 Feb 2021
First published
19 Feb 2021
This article is Open Access

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

Chem. Sci., 2021,12, 5253-5258

Nickel-catalyzed asymmetric reductive arylation of α-chlorosulfones with aryl halides

D. Sun, G. Ma, X. Zhao, C. Lei and H. Gong, Chem. Sci., 2021, 12, 5253 DOI: 10.1039/D1SC00283J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements