Issue 16, 2025

Photo-induced decarboxylative radical cascade cyclization of unactivated alkenes: access to CF- and CF2-substituted ring-fused imidazoles

Abstract

A mild and effective visible-light-induced decarboxylative radical cascade reaction of olefin-containing imidazoles with α-fluorinated carboxylic acids as building blocks containing CF or ArCF2 moieties, has been developed to afford a series of monofluoromethylated or aryldifluoromethylated polycyclic imidazoles in medium to excellent yields with features of simple operation, available raw materials, and wide substrate scopes. In addition, the mechanistic experiments indicated that the methodology involved a radical pathway.

Graphical abstract: Photo-induced decarboxylative radical cascade cyclization of unactivated alkenes: access to CF- and CF2-substituted ring-fused imidazoles

Supplementary files

Article information

Article type
Paper
Submitted
22 Mar 2025
Accepted
09 Apr 2025
First published
22 Apr 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 12739-12745

Photo-induced decarboxylative radical cascade cyclization of unactivated alkenes: access to CF- and CF2-substituted ring-fused imidazoles

H. Wang, S. Lin, H. Hong, Z. Hu, Y. Huang, X. Zhang, S. Lin and B. Yang, RSC Adv., 2025, 15, 12739 DOI: 10.1039/D5RA02023A

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