Chem. J. Chinese Universities

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Photobiocatalytic Radical Acylation Facilitates the Synthesis of β-Ketonitriles

CHE Fuhua1,2,  BAI Jintong2,  HUANG Chunshuai1,2,3*   

  1. 1. School of Pharmacy, Anhui University of Chinese Medicine, Hefei230012,China; 2. Shandong Laboratory of Yantai Drug Discovery, Bohai Rim Advanced Research Institute for Drug Discovery 3. Shanghai Institute of Materia Medica, Chinese Academy of Sciences
  • Received:2026-01-13 Revised:2026-04-07 Online:2026-04-09 Published:2026-04-09
  • Contact: Chunshuai Huang E-mail:huangchunshuai@simm.ac.cn
  • Supported by:
    Supported by the National Natural Science Foundation of China (No. 22407132)

Abstract: This study reports a novel photobiocatalytic system that integrates thiamine diphosphate (ThDP)-dependent enzymes with photoredox catalysis to achieve radical acylation between aromatic aldehydes and azonitrile reagents under visible light irradiation. This method enables the efficient synthesis of β-ketonitriles via cross-coupling of an enzyme-bound ThDP-derived ketyl radical and a photogenerated cyanoalkyl radical under mild conditions. The reaction exhibits a broad substrate scope and good functional group compatibility. This work represents the first example of synthesizing β-ketonitriles via photobiocatalysis, offering a new strategy for sustainable synthesis and expanding the toolbox for non-natural enzyme catalysis.

Key words: Photobiocatalysis, Radical acylation, ThDP, β-Ketonitriles

CLC Number: 

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