Access to Axially Chiral Biaryl Aldehydes via Enantioselective Imine Condensation
Abstract We report herein chiral phosphoric-acid-catalyzed preparation of axially chiral biaryl aldehydes via an unprecedented strategy of enantioselective imine condensation, through either desymmetrization of prochiral substrates or kinetic resolution of racemic atropisomers. The resulting products serve as versatile synthetic intermediates and valuable structural motifs with established applications in asymmetric catalysis and functional materials.
Authors
- Kai Kiat Lau
- Yu Zhao (ORCID: https://orcid.org/0000-0002-2944-1315)
- Jerena C. K. Ng (ORCID: https://orcid.org/0009-0001-7894-6475)
- Thang Minh Le
- Tu Khanh Hung Pham
Institutions
- National University of Singapore (SG)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-10-09
- DOI
- https://doi.org/10.1021/acs.orglett.6c03964
- Primary Topic
- Axial and Atropisomeric Chirality Synthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00