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.
Authors
- Jingping Qü (ORCID: https://orcid.org/0000-0002-7576-0798)
- Xianqing Wu (ORCID: https://orcid.org/0000-0003-1757-0635)
- Zhiming Yu (ORCID: https://orcid.org/0000-0003-0377-1129)
- Tingting Xia
- Yifeng Chen (ORCID: https://orcid.org/0000-0003-3239-6209)
Institutions
- East China University of Science and Technology (CN)
- Chinese Academy of Sciences (CN)
- Shanghai Institute of Organic Chemistry (CN)
- Henan Normal University (CN)
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