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Convergent approach for direct cross-coupling enabled by flash irreversible generation of cationic and anionic species

Author

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  • Hiroki Soutome

    (Hokkaido University
    AGC Inc)

  • Hiroki Yamashita

    (Hokkaido University)

  • Yutaka Shimizu

    (Hokkaido University)

  • Masahiro Takumi

    (Hokkaido University)

  • Yosuke Ashikari

    (Hokkaido University)

  • Aiichiro Nagaki

    (Hokkaido University)

Abstract

In biosynthesis multiple kinds of reactive intermediates are generated, transported, and reacted across different parts of organisms, enabling highly sophisticated synthetic reactions. Herein we report a convergent synthetic approach, which utilizes dual intermediates of cationic and carbanionic species in a single step, hinted at by the ideal reaction conditions. By reactions of unsaturated precursors, such as enamines, with a superacid in a flow microreactor, cationic species, such as iminium ions, are generated rapidly and irreversibly, and before decomposition, they are transported to react with rapidly and independently generated carbanions, enabling direct C-C bond formation. Taking advantage of the reactivity of these double reactive intermediates, the reaction take place within a few seconds, enabling synthetic reactions which are not applicable in conventional reactions.

Suggested Citation

  • Hiroki Soutome & Hiroki Yamashita & Yutaka Shimizu & Masahiro Takumi & Yosuke Ashikari & Aiichiro Nagaki, 2024. "Convergent approach for direct cross-coupling enabled by flash irreversible generation of cationic and anionic species," Nature Communications, Nature, vol. 15(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48723-1
    DOI: 10.1038/s41467-024-48723-1
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