Issue 10, 2025

Distal C–H functionalization of alkoxyarenes through organic photoredox-catalyzed radical–radical coupling

Abstract

We developed a distal C–H functionalization of electron-rich arenes such as alkoxyarenes using diverse coupling partners through organic photoredox catalysis. Our reaction features radical–radical coupling between a cyclohexadienyl radical and various persistent radicals. A range of functional groups, including sp2 carbon-based groups such as alkoxycarbonyl and pyridyl, as well as heteroatom-containing groups like sulfonyl, and alkyl groups were successfully introduced.

Graphical abstract: Distal C–H functionalization of alkoxyarenes through organic photoredox-catalyzed radical–radical coupling

Supplementary files

Article information

Article type
Edge Article
Submitted
12 Dec 2024
Accepted
28 Jan 2025
First published
29 Jan 2025
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., 2025,16, 4320-4327

Distal C–H functionalization of alkoxyarenes through organic photoredox-catalyzed radical–radical coupling

Y. Goto and H. Ohmiya, Chem. Sci., 2025, 16, 4320 DOI: 10.1039/D4SC08407A

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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