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Biomimetic asymmetric catalysis

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Abstract

Enzymes are the core for biological transformations in nature. Their structures and functions have drawn enormous attention from biologists as well as chemists since last century. The large demand of bioactive molecules and the pursuit of efficiency and greenness of synthesis have spurred the rapid development of biomimetic chemistry in the past several decades. Biomimetic asymmetric catalysis, mimicking the structures and functions of enzymes, has been recognized as one of the most promising synthetic strategies for the synthesis of valuable chiral compounds. This review summarizes the evolution of asymmetric catalysis inspired by aldolases, vitamin B1/B6-dependent enzymes, NAD(P)H, flavin, hydrogenases, heme oxygenases, non-heme oxygenases, and dinuclear/multinuclear metalloenzymes in aspects of biomimetic design, catalyst development and related catalytic transformations. Those well-established synthetic approaches originating from biological reactions have demonstrated the unique prowess of biomimetic asymmetric catalysis in bridging the gap between bio-catalysis and chemical synthesis.

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Acknowledgements

This work was supported by the National Natural Science Foundation of China (22231011, 22221002, 22031006, 21831008, 22271192, 92256301, 92256303, 91956116), the NSFC Distinguished Young Scholars (22225107) and the Major Program of the Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences (ZYFZFX-9).

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Authors and Affiliations

  1. State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, 200032, China

    Xiaoming Wang & Kuiling Ding

  2. The Education Ministry Key Laboratory of Resource Chemistry, Shanghai Key Laboratory of Rare Earth Functional Materials, and Shanghai Frontiers Science Center of Biomimetic Catalysis, Shanghai Normal University, Shanghai, 200234, China

    Xiao Xiao & Baoguo Zhao

  3. Center of Basic Molecular Science, Department of Chemistry, Tsinghua University, Beijing, 100084, China

    Kaini Xu & Sanzhong Luo

  4. Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China

    Zhong-Hua Gao & Song Ye

  5. University of Chinese Academy of Sciences, Beijing, 100049, China

    Zhong-Hua Gao, Changqing Ye, Song Ye, Senmiao Xu, Hongli Bao & Wei Sun

  6. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China

    Zhou-Hao Zhu & Yong-Gui Zhou

  7. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, China

    Senmiao Xu & Wei Sun

  8. State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China

    Shou-Fei Zhu

  9. Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, State Key Laboratory of Structural Chemistry, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350002, China

    Changqing Ye & Hongli Bao

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  4. Zhou-Hao Zhu
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  5. Changqing Ye
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  6. Baoguo Zhao
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  8. Song Ye
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Corresponding authors

Correspondence to Baoguo Zhao, Sanzhong Luo, Song Ye, Yong-Gui Zhou, Senmiao Xu, Shou-Fei Zhu, Hongli Bao, Wei Sun, Xiaoming Wang or Kuiling Ding.

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Conflict of interest The authors declare no conflict of interest.

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Xiao, X., Xu, K., Gao, ZH. et al. Biomimetic asymmetric catalysis. Sci. China Chem. 66, 1553–1633 (2023). https://doi.org/10.1007/s11426-023-1578-y

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  • DOI: https://doi.org/10.1007/s11426-023-1578-y

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