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.

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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
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article

Access to Axially Chiral Biaryl Aldehydes via Enantioselective Imine Condensation

Kai Kiat Lau, Yu Zhao, Jerena C. K. Ng, Thang Minh Le et al.
Organic Letters
Axial and Atropisomeric Chirality Synthesis
article

Access to Axially Chiral Biaryl Aldehydes via Enantioselective Imine Condensation

Kai Kiat Lau, Yu Zhao, Jerena C. K. Ng, Thang Minh Le, Tu Khanh Hung Pham
article en

Abstract

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.

Organic Letters
National University of Singapore (SG)
Openalex Percentile: Top 25%
Axial and Atropisomeric Chirality Synthesis
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