Visible-Light-Driven [3 + 2] Annulation of N-Substituted Aromatic Amines with Nitriles: An Approach to Benzimidazoles

A visible-light-driven [3 + 2] annulation of N-substituted aromatic amines with nitriles has been developed, providing efficient access to benzimidazoles. The reaction proceeds under mild conditions with a broad substrate scope and good functional group tolerance. Mechanistic studies support a photoredox-catalyzed radical pathway.

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Publication Details

Journal
Organic Letters
Published
2026-04-22
DOI
https://doi.org/10.1021/acs.orglett.6c01030
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Visible-Light-Driven [3 + 2] Annulation of N-Substituted Aromatic Amines with Nitriles: An Approach to Benzimidazoles

Min Tang, Dongfang Jiang, Xin Xiong, Hao Dong et al.
Organic Letters
Radical Photochemical Reactions
article

Visible-Light-Driven [3 + 2] Annulation of N-Substituted Aromatic Amines with Nitriles: An Approach to Benzimidazoles

Min Tang, Dongfang Jiang, Xin Xiong, Hao Dong, Zhenjie Qi, Jia Zhou, Yutong Tang, Wei-Min He
article en

Abstract

A visible-light-driven [3 + 2] annulation of N-substituted aromatic amines with nitriles has been developed, providing efficient access to benzimidazoles. The reaction proceeds under mild conditions with a broad substrate scope and good functional group tolerance. Mechanistic studies support a photoredox-catalyzed radical pathway.

Organic LettersVol. 28(17)
Jining University (CN), Hunan University of Technology (CN), University of South China (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Openalex Percentile: Top 20%
Radical Photochemical Reactions
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