Chiral Phosphoric Acid‐Catalyzed Atroposelective Synthesis of Axially Chiral Aminophosphines

Comprehensive Summary P,N ‐Atropisomers are valuable structural motifs, widely utilized as chiral ligands and in various catalytic systems. However, the asymmetric synthesis of these compounds from readily available starting materials remains a significant challenge. In this study, we present a chiral phosphoric acid‐catalyzed atroposelective synthesis of axially chiral aminophosphines via dynamic kinetic resolution. This approach effectively addresses the aforementioned challenge through featuring the use of readily available starting materials, mild reaction conditions, high yields, excellent enantioselectivities, and a broad substrate scope, underscoring its practicality and synthetic utility.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-07-25
DOI
https://doi.org/10.1002/cjoc.70197
Citations
1
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.94

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article

Chiral Phosphoric Acid‐Catalyzed Atroposelective Synthesis of Axially Chiral Aminophosphines

Tao‐Yan Lin, X. Liu, Yang Liu, Zihan Wang et al.
1 citations
Chinese Journal of Chemistry
Axial and Atropisomeric Chirality Synthesis
0.94
article

Chiral Phosphoric Acid‐Catalyzed Atroposelective Synthesis of Axially Chiral Aminophosphines

Tao‐Yan Lin, X. Liu, Yang Liu, Zihan Wang, Ruixue Liu, Hui Zhu
article en
1 citations

Abstract

Comprehensive Summary P,N ‐Atropisomers are valuable structural motifs, widely utilized as chiral ligands and in various catalytic systems. However, the asymmetric synthesis of these compounds from readily available starting materials remains a significant challenge. In this study, we present a chiral phosphoric acid‐catalyzed atroposelective synthesis of axially chiral aminophosphines via dynamic kinetic resolution. This approach effectively addresses the aforementioned challenge through featuring the use of readily available starting materials, mild reaction conditions, high yields, excellent enantioselectivities, and a broad substrate scope, underscoring its practicality and synthetic utility.

Chinese Journal of ChemistryVol. 43(22)
Huaibei Normal University (CN), Guizhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 23%
Axial and Atropisomeric Chirality Synthesis
0.94
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Chiral Phosphoric Acid‐Catalyzed Atroposelective Synthesis of Axially Chiral Aminophosphines — Tao‐Yan Lin, X. Liu, et al. · Chinese Journal of Chemistry (2025) | TGRS Research Map | TGRS