Highly Enantioselective Hydrogenation of Imines Catalyzed by Chiral Macrocyclic Boranes
In this paper, we report a macrocyclic alkene-derived borane catalyst for the asymmetric hydrogenation of imines. A wide range of imines was successfully converted to chiral amines in 80-97% yields and 40-97% ee. The macrocyclic framework is indispensable for excellent catalytic activity and enantioselectivity. A gram-scale reaction with 0.2 mol % catalyst loading achieved a turnover number of 485, the highest reported to date for frustrated Lewis pair-catalyzed asymmetric imine hydrogenation.
Authors
- Xiangqing Feng (ORCID: https://orcid.org/0000-0003-1739-925X)
- Haifeng Du
- Ru Zhang
Institutions
- Chinese Academy of Sciences (CN)
- Beijing National Laboratory for Molecular Sciences (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-04-10
- DOI
- https://doi.org/10.1021/acs.orglett.6c00941
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China