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Cobalt-catalyzed aminoalkylative carbonylation of alkenes toward direct synthesis of γ-amino acid derivatives and peptides

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  • Le-Cheng Wang

    (Dalian Institute of Chemical Physics, Chinese Academy of Sciences
    Leibniz-Institut für Katalyse e.V.)

  • Yang Yuan

    (Dalian Institute of Chemical Physics, Chinese Academy of Sciences)

  • Youcan Zhang

    (Dalian Institute of Chemical Physics, Chinese Academy of Sciences)

  • Xiao-Feng Wu

    (Dalian Institute of Chemical Physics, Chinese Academy of Sciences
    Leibniz-Institut für Katalyse e.V.
    University of Chinese Academy of Sciences)

Abstract

γ-Amino acids and peptides analogues are common constituents of building blocks for numerous biologically active molecules, pharmaceuticals, and natural products. In particular, γ-amino acids are providing with better metabolic stability than α-amino acids. Herein we report a multicomponent carbonylation technology that combines readily available amides, alkenes, and the feedstock gas carbon monoxide to build architecturally complex and functionally diverse γ-amino acid derivatives in a single step by the implementation of radical relay catalysis. This transformation can also be used as a late-stage functionalization strategy to deliver complex, advanced γ-amino acid products for pharmaceutical and other areas.

Suggested Citation

  • Le-Cheng Wang & Yang Yuan & Youcan Zhang & Xiao-Feng Wu, 2023. "Cobalt-catalyzed aminoalkylative carbonylation of alkenes toward direct synthesis of γ-amino acid derivatives and peptides," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43306-y
    DOI: 10.1038/s41467-023-43306-y
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