Recent Advances in Organocatalytic Kinetic Resolution for the Synthesis of Axially Chiral Compounds

Axially chiral compounds, indispensable in asymmetric catalysis, drug discovery, and materials science, have witnessed transformative advancements in synthesis through organocatalytic kinetic resolution (OKR) over the past decade. This review systematically dissects the latest achievements (2010-2025) in OKR, focusing on catalyst design, mechanistic insights, substrate diversification, and synthetic applications across C-C biaryl, C-N heterobiaryl, and olefinic axially chiral frameworks. By harnessing non-covalent interactions, OKR has emerged as a powerful strategy to overcome the challenges of low rotational barriers and limited stereocontrol, offering sustainable and enantioselective access to privileged chiral scaffolds. Furthermore, the current challenges and future prospects in this rapidly evolving field are assessed.

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Publication Details

Journal
Molecules
Published
2026-02-26
DOI
https://doi.org/10.3390/molecules31050786
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Recent Advances in Organocatalytic Kinetic Resolution for the Synthesis of Axially Chiral Compounds

Yin Zheng, Liying Cui
Molecules
Axial and Atropisomeric Chirality Synthesis
article

Recent Advances in Organocatalytic Kinetic Resolution for the Synthesis of Axially Chiral Compounds

Yin Zheng, Liying Cui
article en

Abstract

Axially chiral compounds, indispensable in asymmetric catalysis, drug discovery, and materials science, have witnessed transformative advancements in synthesis through organocatalytic kinetic resolution (OKR) over the past decade. This review systematically dissects the latest achievements (2010-2025) in OKR, focusing on catalyst design, mechanistic insights, substrate diversification, and synthetic applications across C-C biaryl, C-N heterobiaryl, and olefinic axially chiral frameworks. By harnessing non-covalent interactions, OKR has emerged as a powerful strategy to overcome the challenges of low rotational barriers and limited stereocontrol, offering sustainable and enantioselective access to privileged chiral scaffolds. Furthermore, the current challenges and future prospects in this rapidly evolving field are assessed.

MoleculesVol. 31(5)
North University of China (CN), Nanjing Forestry University (CN)
Government of Jiangsu Province, Basic Research Program of Jiangsu Province
Responsible consumption and production
Openalex Percentile: Top 40%
Axial and Atropisomeric Chirality Synthesis
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