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.
Authors
- Jun Wang (ORCID: https://orcid.org/0000-0001-9723-4054)
- Li‐Biao Han (ORCID: https://orcid.org/0000-0001-5566-9017)
- Xiaodong Gu (ORCID: https://orcid.org/0009-0006-5088-1127)
- Zhiping Yang (ORCID: https://orcid.org/0000-0003-1396-5218)
Institutions
- Hong Kong Baptist University (HK)
- Minzu University of China (CN)
- Shaoxing University (CN)
- Catalytic Materials (United States) (US)
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
Funders
- Hong Kong Baptist University
- National Natural Science Foundation of China
- Research Grants Council, University Grants Committee
- K. C. Wong Education Foundation