Accessing inherently chiral multifunctional structures by desymmetrization of a wide-rim calix[4]arene triamine

Inherently chiral calix[4]arenes, which have triazole and amine-based functional/receptor groups asymmetrically arranged at the wide rim of a cone macrocycle, can be readily prepared through desymmetrization of a calix[4]arene triamine.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-11-24
DOI
https://doi.org/10.1039/d5qo01509j
Citations
1
Primary Topic
Supramolecular Chemistry and Complexes
Type
article
Field-Weighted Citation Impact
0.94
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article

Accessing inherently chiral multifunctional structures by desymmetrization of a wide-rim calix[4]arene triamine

Dmitry Cheshkov, Stanislav I. Bezzubov, Ivan Alekseev, Еlena V. Kudryashova et al.
1 citations
Organic Chemistry Frontiers
Supramolecular Chemistry and Complexes
0.94
article

Accessing inherently chiral multifunctional structures by desymmetrization of a wide-rim calix[4]arene triamine

Dmitry Cheshkov, Stanislav I. Bezzubov, Ivan Alekseev, Еlena V. Kudryashova, Ivan Vatsouro, Alexander Gorbunov, Elena A. Tarasenko, Vladimir A. Kovalev, Ioann Shugaev
article en
1 citations

Abstract

Inherently chiral calix[4]arenes, which have triazole and amine-based functional/receptor groups asymmetrically arranged at the wide rim of a cone macrocycle, can be readily prepared through desymmetrization of a calix[4]arene triamine.

Organic Chemistry FrontiersVol. 13(3)
Lomonosov Moscow State University (RU), State Research Institute for Chemistry and Technology of Organoelement Compounds (RU), NS Kurnakova Institute of General and Inorganic Chemistry (RU)
Openalex Percentile: Top 19%
Supramolecular Chemistry and Complexes
0.94
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Accessing inherently chiral multifunctional structures by desymmetrization of a wide-rim calix[4]arene triamine — Dmitry Cheshkov, Stanislav I. Bezzubov, et al. · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS