Nickel/Photoredox-Catalyzed Three-Component Dialkylation of Alkenes for the Synthesis of β-Amino Acid Derivatives

Abstract β-Amino acid-containing structures show important biological activity and are found widely in many pharmacologically active compounds; therefore, the development of efficient methods for the synthesis of β-amino acid derivatives has evoked considerable interest in the past decades. Herein, we report a nickel/photoredox-catalyzed synthesis of β-amino acid derivatives from readily available alkyl redox-active esters, alkenes, and α-silylamines. This reaction is characterized by a broad substrate scope, mild conditions, and excellent selectivity. Mechanistic studies suggest that the reaction proceeds through a radical pathway.

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Publication Details

Journal
Synlett
Published
2025-04-08
DOI
https://doi.org/10.1055/a-2577-4281
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Nickel/Photoredox-Catalyzed Three-Component Dialkylation of Alkenes for the Synthesis of β-Amino Acid Derivatives

Weiming Yuan, Ye Fu, Yiqian Yang, Peiwen Liu et al.
1 citations
Synlett
Radical Photochemical Reactions
0.94
article

Nickel/Photoredox-Catalyzed Three-Component Dialkylation of Alkenes for the Synthesis of β-Amino Acid Derivatives

Weiming Yuan, Ye Fu, Yiqian Yang, Peiwen Liu, Wei Gao
article en
1 citations

Abstract

Abstract β-Amino acid-containing structures show important biological activity and are found widely in many pharmacologically active compounds; therefore, the development of efficient methods for the synthesis of β-amino acid derivatives has evoked considerable interest in the past decades. Herein, we report a nickel/photoredox-catalyzed synthesis of β-amino acid derivatives from readily available alkyl redox-active esters, alkenes, and α-silylamines. This reaction is characterized by a broad substrate scope, mild conditions, and excellent selectivity. Mechanistic studies suggest that the reaction proceeds through a radical pathway.

SynlettVol. 36(13)
Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 27%
Radical Photochemical Reactions
0.94
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