Acceleration of [2]Catenane Formation by One of its Rings

Abstract [2]Catenanes were prepared from a crown ether, a diamine, and a diester in moderate to good yields in mild conditions by single‐step, metal‐free active template synthesis. The macrocycle first catalyzes the linear condensation of the diamine and the diester, then it accelerates the cyclization of the bifunctional thread and is incorporated in the catenane, as reported by Zhong et al. ( https://doi.org/10.1002/anov.70004 ).

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Journal
Angewandte Chemie
Published
2025-10-13
DOI
https://doi.org/10.1002/ange.202520104
Primary Topic
Supramolecular Chemistry and Complexes
Type
article
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article

Acceleration of [2]Catenane Formation by One of its Rings

Jean‐Claude Chambron
Angewandte Chemie
Supramolecular Chemistry and Complexes
article

Acceleration of [2]Catenane Formation by One of its Rings

Jean‐Claude Chambron
article en

Abstract

Abstract [2]Catenanes were prepared from a crown ether, a diamine, and a diester in moderate to good yields in mild conditions by single‐step, metal‐free active template synthesis. The macrocycle first catalyzes the linear condensation of the diamine and the diester, then it accelerates the cyclization of the bifunctional thread and is incorporated in the catenane, as reported by Zhong et al. ( https://doi.org/10.1002/anov.70004 ).

Angewandte ChemieVol. 137(46)
Centre National de la Recherche Scientifique (FR), Institut de Chimie de Strasbourg (FR), Université de Strasbourg (FR)
Openalex Percentile: Top 78%
Supramolecular Chemistry and Complexes
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