Catalytic Reductive Addition of Imine for Chiral Amine Synthesis: Recent Advances and Future Perspectives

Abstract Optically active amine represents the most important structure motif in natural products and biologically active compounds. Stereoselective reductive addition of imine with the utilization of electrophilic component offers a concise and operationally simple method for the synthesis of chiral amines. This review mainly highlights recent significant synthetic methodology developments in reductive addition of imine for chiral amine synthesis including chiral auxiliary‐mediated diastereoselective transformation, asymmetric transition metal catalysis, organocatalysis, and enzymatic catalysis. In addition, the electrophilic reagents scopes and mechanistic aspects have also been introduced in this review.

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Publication Details

Journal
ChemCatChem
Published
2024-09-17
DOI
https://doi.org/10.1002/cctc.202401407
Citations
13
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
2.06
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article

Catalytic Reductive Addition of Imine for Chiral Amine Synthesis: Recent Advances and Future Perspectives

Jingping Qü, Xianqing Wu, Zhiming Yu, Tingting Xia et al.
13 citations
ChemCatChem
Asymmetric Hydrogenation and Catalysis
2.06
article

Catalytic Reductive Addition of Imine for Chiral Amine Synthesis: Recent Advances and Future Perspectives

Jingping Qü, Xianqing Wu, Zhiming Yu, Tingting Xia, Yifeng Chen
article en
13 citations

Abstract

Abstract Optically active amine represents the most important structure motif in natural products and biologically active compounds. Stereoselective reductive addition of imine with the utilization of electrophilic component offers a concise and operationally simple method for the synthesis of chiral amines. This review mainly highlights recent significant synthetic methodology developments in reductive addition of imine for chiral amine synthesis including chiral auxiliary‐mediated diastereoselective transformation, asymmetric transition metal catalysis, organocatalysis, and enzymatic catalysis. In addition, the electrophilic reagents scopes and mechanistic aspects have also been introduced in this review.

ChemCatChemVol. 17(1)
East China University of Science and Technology (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN), Henan Normal University (CN)
Openalex Percentile: Top 13%
Asymmetric Hydrogenation and Catalysis
2.06
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Catalytic Reductive Addition of Imine for Chiral Amine Synthesis: Recent Advances and Future Perspectives — Jingping Qü, Xianqing Wu, et al. · ChemCatChem (2024) | TGRS Research Map | TGRS