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.

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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

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article

Highly Enantioselective Hydrogenation of Imines Catalyzed by Chiral Macrocyclic Boranes

Xiangqing Feng, Haifeng Du, Ru Zhang
Organic Letters
Organoboron and organosilicon chemistry
article

Highly Enantioselective Hydrogenation of Imines Catalyzed by Chiral Macrocyclic Boranes

Xiangqing Feng, Haifeng Du, Ru Zhang
article en

Abstract

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.

Organic LettersVol. 28(16)
Chinese Academy of Sciences (CN), Beijing National Laboratory for Molecular Sciences (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 21%
Organoboron and organosilicon chemistry
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