Cross-Electrophile Coupling of Aryl Chlorides with Alkyl Chlorides Using Rotating Magnetic Field and Metal Rods

The pursuit of sustainable and environmentally benign methods and techniques continues to challenge organic chemists. Herein, we report the development of a novel approach in which electromagnetic induction could participate in the coupling of organic chlorides using a rotating magnetic field and metal rods. In particular, we describe the application of this strategy to the nickel-catalyzed cross-electrophile coupling of aryl chlorides with alkyl chlorides. Using these abundant and commercially available organochlorides, such a system allows reactions to proceed with a broader scope than the current protocols under mild conditions.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-04-01
DOI
https://doi.org/10.1021/jacs.5c00381
Citations
12
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
11.23

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article

Cross-Electrophile Coupling of Aryl Chlorides with Alkyl Chlorides Using Rotating Magnetic Field and Metal Rods

Zengdian Zhao, Xiangye Li, Xiaomei Feng, Xinjin Li et al.
12 citations
Journal of the American Chemical Society
Catalytic Cross-Coupling Reactions
11.23
article

Cross-Electrophile Coupling of Aryl Chlorides with Alkyl Chlorides Using Rotating Magnetic Field and Metal Rods

Zengdian Zhao, Xiangye Li, Xiaomei Feng, Xinjin Li, Fenggang Sun, Hui Liu, Ning Zhang, Lizhi Zhang
article en
12 citations

Abstract

The pursuit of sustainable and environmentally benign methods and techniques continues to challenge organic chemists. Herein, we report the development of a novel approach in which electromagnetic induction could participate in the coupling of organic chlorides using a rotating magnetic field and metal rods. In particular, we describe the application of this strategy to the nickel-catalyzed cross-electrophile coupling of aryl chlorides with alkyl chlorides. Using these abundant and commercially available organochlorides, such a system allows reactions to proceed with a broader scope than the current protocols under mild conditions.

Journal of the American Chemical SocietyVol. 147(15)
Shandong University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 1%
Catalytic Cross-Coupling Reactions
11.23
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Cross-Electrophile Coupling of Aryl Chlorides with Alkyl Chlorides Using Rotating Magnetic Field and Metal Rods — Zengdian Zhao, Xiangye Li, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS