Enantioselective reductive cross-couplings to forge C(sp2)–C(sp3) bonds by merging electrochemistry with nickel catalysis
Yun-Zhao Wang,
Bing Sun,
Jian-Feng Guo,
Xiao-Yu Zhu,
Yu-Cheng Gu,
Ya-Ping Han,
Cong Ma and
Tian-Sheng Mei ()
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Yun-Zhao Wang: Chinese Academy of Sciences
Bing Sun: Chinese Academy of Sciences
Jian-Feng Guo: Chinese Academy of Sciences
Xiao-Yu Zhu: Chinese Academy of Sciences
Yu-Cheng Gu: Jealott’s Hill International Research Centre
Ya-Ping Han: Hebei University of Technology
Cong Ma: Chinese Academy of Sciences
Tian-Sheng Mei: Chinese Academy of Sciences
Nature Communications, 2025, vol. 16, issue 1, 1-8
Abstract:
Abstract Motivated by the inherent benefits of synergistically combining electrochemical methodologies with nickel catalysis, we present here a Ni-catalyzed enantioselective electroreductive cross-coupling of benzyl chlorides with aryl halides, yielding chiral 1,1-diaryl compounds with good to excellent enantioselectivity. This catalytic reaction can not only be applied to aryl chlorides/bromides, which are challenging to access by other means, but also to benzyl chlorides containing silicon groups. Additionally, the absence of a sacrificial anode lays a foundation for scalability. The combination of cyclic voltammetry analysis with electrode potential studies suggests that NiI species activate aryl halides via oxidative addition and alkyl chlorides via single electron transfer.
Date: 2025
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DOI: 10.1038/s41467-025-56377-w
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