ARTICLE

Synthesis of Trifluoromethylated Indole/Benzimidazole-Fused Pyrrolidines or Piperidines via Visible-Light-Driven Radical Trifluoromethylation/Cyclization

  • Pan Xiaona ,
  • Wen Huan ,
  • Wang Ke-Hu ,
  • Wang Junjiao ,
  • Huang Danfeng ,
  • Hu Yulai
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  • College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070

Received date: 2026-04-23

  Revised date: 2026-06-02

  Online published: 2026-08-17

Supported by

National Natural Science Foundation of China (No. 22461038).

Abstract

A visible-light-induced radical trifluoromethylation/cyclization reaction of N-isopentenyl/N-4-methyl-3-penten-1-yl-indoles or N-isopentenyl/ N-4-methyl-3-penten-1-yl-benzimidazoles is reported using with CF₃Br as cost-effective and readily available trifluoromethylating reagent. This method enables the efficient construction of trifluoromethyl-substituted indole/benzimidazole-fused pyrrolidine or piperidine derivatives under mild conditions. The protocol exhibits the advantages of high functional group compatibility, a broad substrate scope, and the use of visible light as a green energy source.

Cite this article

Pan Xiaona , Wen Huan , Wang Ke-Hu , Wang Junjiao , Huang Danfeng , Hu Yulai . Synthesis of Trifluoromethylated Indole/Benzimidazole-Fused Pyrrolidines or Piperidines via Visible-Light-Driven Radical Trifluoromethylation/Cyclization[J]. Chinese Journal of Organic Chemistry, 0 : 202604033 . DOI: 10.6023/cjoc202604033

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(马然松,邓周斌,王克虎,黄丹凤,胡雨来,吕肖波,有机化学,2022,43,353)
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