Dual Catalytic Enantioconvergent Carbamoylation of Aziridines

Herein, we disclose an enantioconvergent carbamoylation of racemic aziridines enabled by a dual catalytic strategy. The method offers a new entry point to highly enantioenriched β-amino amides from simple precursors and is characterized by its broad applicability, even with challenging combinations. Preliminary studies with well-defined nickel complexes support a scenario via carbamoyl organometallic intermediates.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-11-20
DOI
https://doi.org/10.1021/jacs.5c15873
Citations
1
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Dual Catalytic Enantioconvergent Carbamoylation of Aziridines

Rubén Martı́n, Tomás G. Santiago, Liangliang Zhang, Huilin Liu
1 citations
Journal of the American Chemical Society
Synthesis and Catalytic Reactions
0.94
article

Dual Catalytic Enantioconvergent Carbamoylation of Aziridines

Rubén Martı́n, Tomás G. Santiago, Liangliang Zhang, Huilin Liu
article en
1 citations

Abstract

Herein, we disclose an enantioconvergent carbamoylation of racemic aziridines enabled by a dual catalytic strategy. The method offers a new entry point to highly enantioenriched β-amino amides from simple precursors and is characterized by its broad applicability, even with challenging combinations. Preliminary studies with well-defined nickel complexes support a scenario via carbamoyl organometallic intermediates.

Journal of the American Chemical SocietyVol. 147(48)
Institució Catalana de Recerca i Estudis Avançats (ES), Institut Català d'Investigació Química (ES), Universitat Rovira i Virgili (ES)
Openalex Percentile: Top 20%
Synthesis and Catalytic Reactions
0.94
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