Enantioselective Synthesis of Axially Chiral Tetraphenylethenes via NHC-Catalyzed Desymmetrization and Following Kinetic Resolution

Abstract Herein, we report an efficient method for the enantioselective construction of axially chiral tetraphenylethylene (TPE) via N-heterocyclic carbene (NHC)-catalyzed desymmetrization of prochiral isophthalaldehyde-derived TPEs. Both aliphatic alcohols and phenols were well-tolerated, affording the atropisomeric TPEs in good yields and enantioselectivities. Mechanistic investigations reveal that desymmetrization is a key contributor to enantioselective control, and the following kinetic resolution further enhances the enantioselectivity. Gram-scale synthesis and late-stage functionalization of pharmaceuticals further validated the practicality and potential of this method.

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Publication Details

Journal
Organic Letters
Published
2026-10-08
DOI
https://doi.org/10.1021/acs.orglett.6c03899
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
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article

Enantioselective Synthesis of Axially Chiral Tetraphenylethenes via NHC-Catalyzed Desymmetrization and Following Kinetic Resolution

Chun-Lin Zhang, Xin-Han Wang, Song Ye
Organic Letters
Axial and Atropisomeric Chirality Synthesis
article

Enantioselective Synthesis of Axially Chiral Tetraphenylethenes via NHC-Catalyzed Desymmetrization and Following Kinetic Resolution

Chun-Lin Zhang, Xin-Han Wang, Song Ye
article en

Abstract

Abstract Herein, we report an efficient method for the enantioselective construction of axially chiral tetraphenylethylene (TPE) via N-heterocyclic carbene (NHC)-catalyzed desymmetrization of prochiral isophthalaldehyde-derived TPEs. Both aliphatic alcohols and phenols were well-tolerated, affording the atropisomeric TPEs in good yields and enantioselectivities. Mechanistic investigations reveal that desymmetrization is a key contributor to enantioselective control, and the following kinetic resolution further enhances the enantioselectivity. Gram-scale synthesis and late-stage functionalization of pharmaceuticals further validated the practicality and potential of this method.

Organic Letters
Chinese Academy of Sciences (CN), Institute of Chemistry (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 25%
Axial and Atropisomeric Chirality Synthesis
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Enantioselective Synthesis of Axially Chiral Tetraphenylethenes via NHC-Catalyzed Desymmetrization and Following Kinetic Resolution — Chun-Lin Zhang, Xin-Han Wang, et al. · Organic Letters (2026) | TGRS Research Map | TGRS