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Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis
Inherently chiral calixarenes, whose chirality is based on the absence of a planar symmetry or an inversion center in the molecules as a whole through the asymmetric array of several achiral groups upon the three-dimensional calix-skeletons, are challenging and attractive chiral molecules, because o...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International (MDPI)
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039962/ https://www.ncbi.nlm.nih.gov/pubmed/21339996 http://dx.doi.org/10.3390/ijms12010429 |
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author | Li, Shao-Yong Xu, Yao-Wei Liu, Jun-Min Su, Cheng-Yong |
author_facet | Li, Shao-Yong Xu, Yao-Wei Liu, Jun-Min Su, Cheng-Yong |
author_sort | Li, Shao-Yong |
collection | PubMed |
description | Inherently chiral calixarenes, whose chirality is based on the absence of a planar symmetry or an inversion center in the molecules as a whole through the asymmetric array of several achiral groups upon the three-dimensional calix-skeletons, are challenging and attractive chiral molecules, because of their potential in supramolecular chemistry. The synthesis and optical resolution of all varieties of inherently chiral calixarenes are systematically discussed and classified, and their applications in chiral recognition and asymmetric catalysis are thoroughly illustrated in this review. |
format | Text |
id | pubmed-3039962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-30399622011-02-18 Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis Li, Shao-Yong Xu, Yao-Wei Liu, Jun-Min Su, Cheng-Yong Int J Mol Sci Review Inherently chiral calixarenes, whose chirality is based on the absence of a planar symmetry or an inversion center in the molecules as a whole through the asymmetric array of several achiral groups upon the three-dimensional calix-skeletons, are challenging and attractive chiral molecules, because of their potential in supramolecular chemistry. The synthesis and optical resolution of all varieties of inherently chiral calixarenes are systematically discussed and classified, and their applications in chiral recognition and asymmetric catalysis are thoroughly illustrated in this review. Molecular Diversity Preservation International (MDPI) 2011-01-17 /pmc/articles/PMC3039962/ /pubmed/21339996 http://dx.doi.org/10.3390/ijms12010429 Text en © 2011 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Li, Shao-Yong Xu, Yao-Wei Liu, Jun-Min Su, Cheng-Yong Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis |
title | Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis |
title_full | Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis |
title_fullStr | Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis |
title_full_unstemmed | Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis |
title_short | Inherently Chiral Calixarenes: Synthesis, Optical Resolution, Chiral Recognition and Asymmetric Catalysis |
title_sort | inherently chiral calixarenes: synthesis, optical resolution, chiral recognition and asymmetric catalysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039962/ https://www.ncbi.nlm.nih.gov/pubmed/21339996 http://dx.doi.org/10.3390/ijms12010429 |
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