Synlett
DOI: 10.1055/a-2716-2853
Letter

Nickel-Catalyzed Enantioconvergent Cycloadditions of Aziridines and Imines

Authors

  • Toshifumi Takahashi

    1   Department of Chemistry, Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Japan (Ringgold ID: RIN12907)
  • Rihoko Tonbe

    1   Department of Chemistry, Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Japan (Ringgold ID: RIN12907)
  • Daishi Hiramatsu

    1   Department of Chemistry, Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Japan (Ringgold ID: RIN12907)
  • Takuya Kurahashi

    1   Department of Chemistry, Graduate School of Science and Technology, Kwansei Gakuin University, Sanda, Japan (Ringgold ID: RIN12907)

Supported by: Masuyakinen Basic Research Foundation
Supported by: Grants-in-Aid for Scientific Research from MEXT (Japan) 20H02737,23K20277
Supported by: Kumagai Science and Technology Foundation
Supported by: Toshiaki Ogasawara Memorial Foundation
Supported by: Murata Science Foundation
Supported by: Iketani Science and Technology Foundation
Funding Information This work was supported by Grants-in-Aid for Scientific Research (Nos. 20H02737, and 23K20277) from MEXT (Japan). We acknowledge the Masuyakinen Basic Research Foundation, Murata Science Foundation, Toshiaki Ogasawara Memorial Foundation, Kumagai Science and Technology Foundation, and Iketani Science and Technology Foundation.


Graphical Abstract

Abstract

We report asymmetric nickel-catalyzed cycloadditions of aziridines and imines enabled by a newly designed tyrosine-derived FOXAP ligand, delivering up to 97% ee and >20:1 dr. The reaction constructs imidazolidines bearing two nonadjacent stereocenters from racemic vinylaziridines and achiral imines in an enantioconvergent manner.



Publication History

Received: 13 September 2025

Accepted after revision: 30 September 2025

Article published online:
31 October 2025

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