Modular Assembly of Axially Chiral QUINAP Derivatives via Nickel-Catalyzed Enantioselective C–P Cross-Coupling

QUINAPs represent a powerful class of ligands with broad applications in a diverse array of synthetically important asymmetric transformations. However, their broader utilization is often constrained by a limited substrate scope and high cost associated with their multistep synthesis. Consequently, a highly efficient dynamic kinetic asymmetric transformation of N-heterobiaryl derivatives has been developed through Ni-catalyzed asymmetric C–P cross-coupling. This method provides versatile access to a wide range of substituted QUINAP derivatives with good yields and high enantioselectivities, which are successfully applied in both transition-metal catalysis and organocatalysis.

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Publication Details

Journal
ACS Catalysis
Published
2025-05-02
DOI
https://doi.org/10.1021/acscatal.5c01663
Citations
10
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
9.36

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article

Modular Assembly of Axially Chiral QUINAP Derivatives via Nickel-Catalyzed Enantioselective C–P Cross-Coupling

Jun Wang, Li‐Biao Han, Xiaodong Gu, Zhiping Yang
10 citations
ACS Catalysis
Axial and Atropisomeric Chirality Synthesis
9.36
article

Modular Assembly of Axially Chiral QUINAP Derivatives via Nickel-Catalyzed Enantioselective C–P Cross-Coupling

Jun Wang, Li‐Biao Han, Xiaodong Gu, Zhiping Yang
article en
10 citations

Abstract

QUINAPs represent a powerful class of ligands with broad applications in a diverse array of synthetically important asymmetric transformations. However, their broader utilization is often constrained by a limited substrate scope and high cost associated with their multistep synthesis. Consequently, a highly efficient dynamic kinetic asymmetric transformation of N-heterobiaryl derivatives has been developed through Ni-catalyzed asymmetric C–P cross-coupling. This method provides versatile access to a wide range of substituted QUINAP derivatives with good yields and high enantioselectivities, which are successfully applied in both transition-metal catalysis and organocatalysis.

ACS CatalysisVol. 15(10)
Hong Kong Baptist University (HK), Minzu University of China (CN), Shaoxing University (CN), Catalytic Materials (United States) (US)
Hong Kong Baptist University, National Natural Science Foundation of China, Research Grants Council, University Grants Committee, K. C. Wong Education Foundation
Openalex Percentile: Top 2%
Axial and Atropisomeric Chirality Synthesis
9.36
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