Nickel-Catalyzed Enantioconvergent Cycloadditions of Aziridines and Imines

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.

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Publication Details

Journal
Synlett
Published
2025-10-31
DOI
https://doi.org/10.1055/a-2716-2853
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Nickel-Catalyzed Enantioconvergent Cycloadditions of Aziridines and Imines

Takuya Kurahashi, Toshifumi Takahashi, Rihoko Tonbe, Daishi Hiramatsu
Synlett
Synthesis and Catalytic Reactions
article

Nickel-Catalyzed Enantioconvergent Cycloadditions of Aziridines and Imines

Takuya Kurahashi, Toshifumi Takahashi, Rihoko Tonbe, Daishi Hiramatsu
article en

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.

SynlettVol. 37(03)
Kwansei Gakuin University (JP)
Openalex Percentile: Top 76%
Synthesis and Catalytic Reactions
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Nickel-Catalyzed Enantioconvergent Cycloadditions of Aziridines and Imines — Takuya Kurahashi, Toshifumi Takahashi, et al. · Synlett (2025) | TGRS Research Map | TGRS