Chemoselective nickel-catalyzed difluoromethylation of aryl halides with (SIPr)AgCF2H as transmetalation reagent

Abstract

A user-friendly method for the difluoromethylation of aryl iodides under nickel catalysis has been developed, employing readily accessible, light- and temperature-insensitive (SIPr)AgCF2H as CF2H source. A variety of electronically diverse arenes was smoothly transformed and the reaction displayed excellent levels of chemoselectivity, tolerating inter alia synthetically valuable triflates.

Graphical abstract: Chemoselective nickel-catalyzed difluoromethylation of aryl halides with (SIPr)AgCF2H as transmetalation reagent

Supplementary files

Article information

Article type
Communication
Submitted
14 Nov 2025
Accepted
08 Dec 2025
First published
08 Dec 2025
This article is Open Access
Creative Commons BY license

Chem. Commun., 2026, Advance Article

Chemoselective nickel-catalyzed difluoromethylation of aryl halides with (SIPr)AgCF2H as transmetalation reagent

T. Rogge, Chem. Commun., 2026, Advance Article , DOI: 10.1039/D5CC06479A

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