Photo/Copper-Catalyzed Sulfinamidation of Arenes and Alkenes

Aryl sulfinamides are valuable intermediates and functional motifs in organic synthesis, with broad utility in pharmaceutical and agrochemical development. However, their broader application has been limited by underdeveloped synthetic methods, often requiring conventionally prefunctionalized aryl/alkenyl halides or organometallic reagents, protected sulfinylamine reagents, and harsh reaction conditions. Herein, we report a photo/copper-catalyzed sulfinamidation of arenes and alkenes, employing aryl and alkenyl sulfonium salts as radical linchpins. This protocol proceeds under mild conditions, exhibits broad functional group tolerance, and enables highly regioselective late-stage functionalization of complex molecules. The method provides streamlined access to diverse aryl S(IV) and S(VI) derivatives, offering a powerful platform for drug discovery and the modular synthesis of bioactive compounds.

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Publication Details

Journal
Organic Letters
Published
2025-08-28
DOI
https://doi.org/10.1021/acs.orglett.5c03252
Citations
6
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
5.62

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article

Photo/Copper-Catalyzed Sulfinamidation of Arenes and Alkenes

Weihua Yang, Yujian Mao, Xiao-Bin Dai, Fei Xue et al.
6 citations
Organic Letters
Sulfur-Based Synthesis Techniques
5.62
article

Photo/Copper-Catalyzed Sulfinamidation of Arenes and Alkenes

Weihua Yang, Yujian Mao, Xiao-Bin Dai, Fei Xue, Jianming Yan, Xiaojin Jiao, Wenwen Li, Jialin Liu, Li‐Han Zhao, Dan Liu, Feihu Liu, Ning Ding, Aishun Ding, Jing Ren, Rongli Qiu, Jingmei Hu
article en
6 citations

Abstract

Aryl sulfinamides are valuable intermediates and functional motifs in organic synthesis, with broad utility in pharmaceutical and agrochemical development. However, their broader application has been limited by underdeveloped synthetic methods, often requiring conventionally prefunctionalized aryl/alkenyl halides or organometallic reagents, protected sulfinylamine reagents, and harsh reaction conditions. Herein, we report a photo/copper-catalyzed sulfinamidation of arenes and alkenes, employing aryl and alkenyl sulfonium salts as radical linchpins. This protocol proceeds under mild conditions, exhibits broad functional group tolerance, and enables highly regioselective late-stage functionalization of complex molecules. The method provides streamlined access to diverse aryl S(IV) and S(VI) derivatives, offering a powerful platform for drug discovery and the modular synthesis of bioactive compounds.

Organic LettersVol. 27(36)
Nanjing University of Chinese Medicine (CN), China Pharmaceutical University (CN), Nanjing Forestry University (CN)
Chongqing Medical University, Natural Science Foundation of Jiangsu Province, Jiangsu Provincial Department of Education, Nanjing University of Chinese Medicine
Openalex Percentile: Top 4%
Sulfur-Based Synthesis Techniques
5.62
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