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

[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 International Edition
Published
2025-10-13
DOI
https://doi.org/10.1002/anie.202520104
Primary Topic
Chemical Synthesis and Analysis
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article
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article

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

Jean‐Claude Chambron
Angewandte Chemie International Edition
Chemical Synthesis and Analysis
article

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

Jean‐Claude Chambron
article en

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 Chemie International EditionVol. 64(46)
Centre National de la Recherche Scientifique (FR), Institut de Chimie de Strasbourg (FR), Université de Strasbourg (FR)
Openalex Percentile: Top 74%
Chemical Synthesis and Analysis
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