Electrochemical Nickel-Catalyzed Cross-Electrophile Coupling: A Sustainable Platform for C(sp3)–C(sp3)/C(sp2) Bond Construction

Abstract An electrochemical nickel-catalyzed cross-electrophile coupling reaction of organic halides with cyclosulfonium salts to construct C(sp3)–C(sp3)/C(sp2) bonds is reported. This highly selective synthetic approach demonstrates significant practical utility, as evidenced by its broad substrate scope encompassing C(sp3)–/C(sp2)–iodides, while maintaining excellent functional group tolerance, particularly challenging late-stage functionalization applications. Moreover, density functional theory (DFT) calculations are employed to systematically evaluate the Gibbs free energy profile of key intermediates along the proposed nickel-catalyzed reaction pathway, thereby providing robust theoretical support for the mechanistic feasibility of the transformation.

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Publication Details

Journal
Organic Letters
Published
2026-09-06
DOI
https://doi.org/10.1021/acs.orglett.6c03121
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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Electrochemical Nickel-Catalyzed Cross-Electrophile Coupling: A Sustainable Platform for C(sp3)–C(sp3)/C(sp2) Bond Construction

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Electrochemical Nickel-Catalyzed Cross-Electrophile Coupling: A Sustainable Platform for C(sp3)–C(sp3)/C(sp2) Bond Construction

Qiang Xiao, Mu‐Jia Luo, L.Y. Wang, Jinxia Li, Huang Yong-fei, Chaozhihui Cheng, Miao Yan
article en

Abstract

Abstract An electrochemical nickel-catalyzed cross-electrophile coupling reaction of organic halides with cyclosulfonium salts to construct C(sp3)–C(sp3)/C(sp2) bonds is reported. This highly selective synthetic approach demonstrates significant practical utility, as evidenced by its broad substrate scope encompassing C(sp3)–/C(sp2)–iodides, while maintaining excellent functional group tolerance, particularly challenging late-stage functionalization applications. Moreover, density functional theory (DFT) calculations are employed to systematically evaluate the Gibbs free energy profile of key intermediates along the proposed nickel-catalyzed reaction pathway, thereby providing robust theoretical support for the mechanistic feasibility of the transformation.

Organic Letters
Xinjiang Normal University (CN), Changzhi Medical College (CN), Xinzhou Teachers University (CN), Jiangxi Science and Technology Normal University (CN)
National Natural Science Foundation of China, Jiangxi Science and Technology Normal University
Responsible consumption and production
Openalex Percentile: Top 20%
Catalytic Cross-Coupling Reactions
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