Remote α- and β-C(sp 3 )–H alkenylation of amines via visible-light supported paired electrolysis

Read full text
Authors: Siddharth K. Dave, Sebastian Stecko
Cited by: 1
References: 109

Abstract

, a XAT reagent capable of activation of aryl halide to provide aryl radical species. Cathodic reduction of a Ni(i) intermediate to the Ni(0) complex allows closing the Ni-catalyzed cycle, enabling the execution of the cross-coupling stage leading to a C-H functionalized amine derivative. The developed conditions enable precise synchronization of anodic and cathodic catalytic cycles occurring in the presented variant of paired electrolysis, which has been a significant challenge until now.

Fields of Study & Subjects

Radical Photochemical Reactions Catalytic C–H Functionalization Methods Sulfur-Based Synthesis Techniques

Publication details

Journal / source
Chemical Science
Publisher
Royal Society of Chemistry (RSC)
Volume
17
Issue
12
Pages
6017–6042
Publication date
1 January 2026
Language
EN