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Synthesis
DOI: 10.1055/a-2649-4768
DOI: 10.1055/a-2649-4768
Paper
Nickel-Catalyzed Reductive Cross-Coupling of Imines with α-Imino Esters for the Construction of α,β-Diamino Acid Derivatives
Supported by: National Natural Science Foundation of China 22471067
Supported by: Fundamental Research Funds for the Central Universities
This research was funded by the National Natural Science Foundation of China (22471067), the Natural Science Foundation of Hunan Province (2022JJ20006), and the Fundamental Research Funds for the Central Universities.

Abstract
A nickel-catalyzed reductive cross-coupling reaction of different imines has been developed. This method enables the first reductive cross-coupling between aryl/alkyl imines and α-imino esters, affording α,β-diamino acid derivatives bearing quaternary carbon centers in a single-step process. This imine umpolung strategy exhibits several advantages, such as mild conditions and broad functional group compatibility.
Keywords
Nickel catalysis - Imines - α-Imino esters - Reductive cross-coupling - α,β-Diamino acid derivativesPublication History
Received: 29 May 2025
Accepted after revision: 04 July 2025
Article published online:
08 August 2025
© 2025. Thieme. All rights reserved.
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