Synthesis
DOI: 10.1055/a-2733-1592
Paper

Electrochemically Catalyzed Decarboxylative Borylation of (Hetero)Aryl Carboxylic Acids

Authors

  • Yan Tian

    1   School of Inspection, Testing, and Certification, Changzhou Vocational Institute of Engineering, Changzhou, China (Ringgold ID: RIN164388)
    2   College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, China (Ringgold ID: RIN12475)
  • Yingchao Li

    1   School of Inspection, Testing, and Certification, Changzhou Vocational Institute of Engineering, Changzhou, China (Ringgold ID: RIN164388)
  • Yucan He

    1   School of Inspection, Testing, and Certification, Changzhou Vocational Institute of Engineering, Changzhou, China (Ringgold ID: RIN164388)
  • Zu Xu

    1   School of Inspection, Testing, and Certification, Changzhou Vocational Institute of Engineering, Changzhou, China (Ringgold ID: RIN164388)
  • Yulu Yuan

    1   School of Inspection, Testing, and Certification, Changzhou Vocational Institute of Engineering, Changzhou, China (Ringgold ID: RIN164388)
  • Bo Xu

    2   College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, China (Ringgold ID: RIN12475)
  • Xianqiang Kong

    3   School of Chemical Engineering and Materials, Changzhou Institute of Technology, Changzhou, China (Ringgold ID: RIN164387)

Supported by: National Natural Science Foundation of China 22202021,22372015
Supported by: Changzhou Vocational Institute of Engineering 11130900122004
Funding Information This work was financially supported by National Natural Science Foundation of China (NSFC22202021 and 22372015), the Young Backbone Teachers Fund of Jiangsu Qinglan Project, and the School research fund of Changzhou Vocational Institute of Engineering (11130900122004).


Graphical Abstract

Abstract

A straightforward and efficient electrochemical method for the decarboxylative borylation of (hetero)aryl carboxylic acids has been outlined. This metal-/base-/oxidant-free strategy enables efficient access to arylboronate esters, demonstrating a broad substrate scope (20 examples) with yields of up to 62% while maintaining exceptional atom- and step-economy.



Publication History

Received: 30 April 2025

Accepted after revision: 27 October 2025

Accepted Manuscript online:
27 October 2025

Article published online:
14 November 2025

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