Recognition of Chiral Carboxylic Anions by Artificial Receptors

Many carboxylic molecules, ranging from drugs to flavors and fragrances, contain chiral centers. As a consequence, research has been carried out in order to design and synthesize artificial receptors for carboxylic anions. Many problems have to be solved for binding anions. The results obtained in t...

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Detalles Bibliográficos
Autores principales: Dieng, Pape Sylla, Sirlin, Claude
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956098/
https://www.ncbi.nlm.nih.gov/pubmed/20957098
http://dx.doi.org/10.3390/ijms11093334
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author Dieng, Pape Sylla
Sirlin, Claude
author_facet Dieng, Pape Sylla
Sirlin, Claude
author_sort Dieng, Pape Sylla
collection PubMed
description Many carboxylic molecules, ranging from drugs to flavors and fragrances, contain chiral centers. As a consequence, research has been carried out in order to design and synthesize artificial receptors for carboxylic anions. Many problems have to be solved for binding anions. The results obtained in the binding of carboxylic anions by guanidine, secondary ammonium and metal-center have been selected. The last part of this review focuses on chiral recognition of carboxylic anions by organic and metal-based chiral receptors.
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spelling pubmed-29560982010-10-18 Recognition of Chiral Carboxylic Anions by Artificial Receptors Dieng, Pape Sylla Sirlin, Claude Int J Mol Sci Review Many carboxylic molecules, ranging from drugs to flavors and fragrances, contain chiral centers. As a consequence, research has been carried out in order to design and synthesize artificial receptors for carboxylic anions. Many problems have to be solved for binding anions. The results obtained in the binding of carboxylic anions by guanidine, secondary ammonium and metal-center have been selected. The last part of this review focuses on chiral recognition of carboxylic anions by organic and metal-based chiral receptors. Molecular Diversity Preservation International (MDPI) 2010-09-15 /pmc/articles/PMC2956098/ /pubmed/20957098 http://dx.doi.org/10.3390/ijms11093334 Text en © 2010 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
Dieng, Pape Sylla
Sirlin, Claude
Recognition of Chiral Carboxylic Anions by Artificial Receptors
title Recognition of Chiral Carboxylic Anions by Artificial Receptors
title_full Recognition of Chiral Carboxylic Anions by Artificial Receptors
title_fullStr Recognition of Chiral Carboxylic Anions by Artificial Receptors
title_full_unstemmed Recognition of Chiral Carboxylic Anions by Artificial Receptors
title_short Recognition of Chiral Carboxylic Anions by Artificial Receptors
title_sort recognition of chiral carboxylic anions by artificial receptors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956098/
https://www.ncbi.nlm.nih.gov/pubmed/20957098
http://dx.doi.org/10.3390/ijms11093334
work_keys_str_mv AT diengpapesylla recognitionofchiralcarboxylicanionsbyartificialreceptors
AT sirlinclaude recognitionofchiralcarboxylicanionsbyartificialreceptors

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