Issue 45, 2022

Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer

Abstract

Sulfoximines are synthetically important scaffolds and serve important roles in drug discovery. Currently, there is no solution to decarboxylative sulfoximination of benzoic acids; although thoroughly investigated, limited substrate scope and harsh reaction conditions still hold back traditional thermal aromatic decarboxylative functionalization. Herein, we realize the first decarboxylative sulfoximination of benzoic acids via photo-induced ligand to copper charge transfer (copper-LMCT)-enabled decarboxylative carbometalation. The transformation proceeds under mild reaction conditions, has a broad substrate scope, and can be applied to late-stage functionalization of complex small molecules.

Graphical abstract: Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer

Supplementary files

Article information

Article type
Edge Article
Submitted
29 Sep 2022
Accepted
01 Nov 2022
First published
14 Nov 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 license

Chem. Sci., 2022,13, 13611-13616

Decarboxylative sulfoximination of benzoic acids enabled by photoinduced ligand-to-copper charge transfer

P. Xu, W. Su and T. Ritter, Chem. Sci., 2022, 13, 13611 DOI: 10.1039/D2SC05442F

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.

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