Catalytic Enantioselective Construction of Planar Chiral Heterocyclic [2.2]Paracyclophanes Enabled by Copper-Catalyzed Desymmetric Azide-Alkyne Cycloaddition
The construction of planar chiral [2.2]paracyclophanes (PCPs) is of great importance due to their intriguing photophysical and optoelectronic properties. However, catalytic asymmetric approaches to access valuable heterocyclic PCPs directly remain underexplored. Herein, we present the enantioselective synthesis of planar chiral triazole-based PCPs via a desymmetrizing copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction. A diverse range of functionalized optically enriched heterocyclic PCPs is obtained in a highly enantioselective manner under mild conditions. Moreover, this protocol showcases the versatility and efficiency of applying the desymmetric CuAAC reaction in the successful construction of planar chirality. Catalytic asymmetric approaches to access valuable heterocyclic [2.2]paracyclophanes directly remain underexplored. Herein, the authors present the enantioselective synthesis of planar chiral triazole-based [2.2]paracyclophanes via a desymmetrizing copper-catalyzed alkyne-azide cycloaddition reaction.
Authors
- Feng Yuan-mei
- Kefeng Zhang (ORCID: https://orcid.org/0000-0003-4066-6299)
- Zhuang-Zhuang Li
Institutions
- Huaibei Normal University (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-06-25
- DOI
- https://doi.org/10.1038/s41467-026-74663-z
- Primary Topic
- Synthesis and Properties of Aromatic Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Universität Basel
- Université de Genève
- Zaozhuang University
- Anhui Normal University
- Natural Science Foundation of Anhui Province