Photoredox-Catalyzed [2 + 1 + 2] Cyclization of Alkenes, Carbyne Equivalents, and Nitriles

We present an unprecedented light-driven three-component [2 + 1 + 2] cyclization that integrates carbyne equivalents with readily available nitriles and alkenes. Mechanistic validation through the isolation of a key intermediate reveals a cascade sequence: photoinduced diazomethyl radical generation, concerted cyclization, and subsequent acid-promoted aromatization. This catalytic paradigm enables modular synthesis of unprotected tetrasubstituted pyrroles with complete regioselectivity, eliminating traditional multistep manipulations. Furthermore, we developed a skeletal editing strategy that overcomes the challenge of converting pyrrole cores into polysubstituted naphthalenes. Combined with established skeletal diversification protocols (pyrrole-to-benzene/pyridine conversions), these transformations collectively demonstrate the remarkable plasticity of pyrrole cores in the construction of highly functionalized aromatic systems.

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Publication Details

Journal
ACS Catalysis
Published
2025-05-30
DOI
https://doi.org/10.1021/acscatal.5c02051
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Photoredox-Catalyzed [2 + 1 + 2] Cyclization of Alkenes, Carbyne Equivalents, and Nitriles

Zhanyong Tang, Xiaoqiang Ma, Depeng Zhao, Xingda Zhao et al.
1 citations
ACS Catalysis
Radical Photochemical Reactions
0.94
article

Photoredox-Catalyzed [2 + 1 + 2] Cyclization of Alkenes, Carbyne Equivalents, and Nitriles

Zhanyong Tang, Xiaoqiang Ma, Depeng Zhao, Xingda Zhao, Jialin Huang
article en
1 citations

Abstract

We present an unprecedented light-driven three-component [2 + 1 + 2] cyclization that integrates carbyne equivalents with readily available nitriles and alkenes. Mechanistic validation through the isolation of a key intermediate reveals a cascade sequence: photoinduced diazomethyl radical generation, concerted cyclization, and subsequent acid-promoted aromatization. This catalytic paradigm enables modular synthesis of unprotected tetrasubstituted pyrroles with complete regioselectivity, eliminating traditional multistep manipulations. Furthermore, we developed a skeletal editing strategy that overcomes the challenge of converting pyrrole cores into polysubstituted naphthalenes. Combined with established skeletal diversification protocols (pyrrole-to-benzene/pyridine conversions), these transformations collectively demonstrate the remarkable plasticity of pyrrole cores in the construction of highly functionalized aromatic systems.

ACS CatalysisVol. 15(12)
Sun Yat-sen University (CN)
National Natural Science Foundation of China, Sun Yat-sen University, Guangdong Province Introduction of Innovative R&D Team
Openalex Percentile: Top 25%
Radical Photochemical Reactions
0.94
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