Dual photoredox/copper-catalyzed selective difluoromethylthiolation of remote unactivated C(sp3)–H bonds at room temperature

Abstract

A photocatalysis/copper dual-catalyzed difluoromethylthiolation of remote unactivated C(sp3)–H bonds using N-fluorosulfonamides was reported. The combination of photoredox and copper catalysis led to mild reaction conditions with a broad substrate scope. Luminescence quenching experiments revealed that both N-fluorosulfonamides and the copper catalyst could quench the excited state of the Ru complex. Primary, secondary and tertiary C(sp3)–H bonds could be transformed, offering an efficient way to construct difluoromethylthio-bearing compounds.

Graphical abstract: Dual photoredox/copper-catalyzed selective difluoromethylthiolation of remote unactivated C(sp3)–H bonds at room temperature

Supplementary files

Article information

Article type
Paper
Submitted
13 Feb 2025
Accepted
19 May 2025
First published
20 May 2025

Org. Biomol. Chem., 2025, Advance Article

Dual photoredox/copper-catalyzed selective difluoromethylthiolation of remote unactivated C(sp3)–H bonds at room temperature

S. Li, G. Ji, W. Wang and S. Wang, Org. Biomol. Chem., 2025, Advance Article , DOI: 10.1039/D5OB00257E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements