Volume 42, Issue 19 pp. 2323-2328
Concise Report

Photochemical Radical Cascade 6-endo Cyclization of Dienes with α-Carbonyl Bromides for the Synthesis of Six-Membered Benzo-Fused Lactams

Jia-Li Sui

Jia-Li Sui

Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, Hunan, 414006 China

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Yang Guo

Yang Guo

Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, Hunan, 414006 China

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Bi-Quan Xiong

Bi-Quan Xiong

Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, Hunan, 414006 China

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Ke-Wen Tang

Ke-Wen Tang

Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, Hunan, 414006 China

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Peng-Fei Huang

Corresponding Author

Peng-Fei Huang

Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, Hunan, 414006 China

E-mail: [email protected]; [email protected]; [email protected]Search for more papers by this author
Yu Liu

Corresponding Author

Yu Liu

Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, Hunan, 414006 China

E-mail: [email protected]; [email protected]; [email protected]Search for more papers by this author
Jin-Heng Li

Corresponding Author

Jin-Heng Li

State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, 266042 China

E-mail: [email protected]; [email protected]; [email protected]Search for more papers by this author
First published: 22 May 2024
Citations: 3

These authors contributed equally to this work.

Comprehensive Summary

A novel visible-light-induced radical cascade 6-endo cyclization of dienes (N-(2-vinylphenyl)acryl amides) is developed utilizing α-carbonyl bromides as alkyl reagents. This approach affords an efficient way for synthesizing six-membered benzo-fused lactam derivatives with chemo- and regio-selectivity and good functional group tolerance. Primary, secondary, and tertiary bromides are well-compatible with this cascade cyclization reaction.

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