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The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives
New dissymmetric and asymmetric p-tert-butylthiacalix[4]arene derivatives were prepared as a result of the reaction of p-tert-butylthiacalix[4]arene with diethyl bromomalonate in the presence of different alkali metals (Cs, K and Na) in refluxing acetone for 7 days. The structures of the prepared co...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254204/ https://www.ncbi.nlm.nih.gov/pubmed/19471195 http://dx.doi.org/10.3390/molecules14051755 |
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author | Omran, Omran Abdellah |
author_facet | Omran, Omran Abdellah |
author_sort | Omran, Omran Abdellah |
collection | PubMed |
description | New dissymmetric and asymmetric p-tert-butylthiacalix[4]arene derivatives were prepared as a result of the reaction of p-tert-butylthiacalix[4]arene with diethyl bromomalonate in the presence of different alkali metals (Cs, K and Na) in refluxing acetone for 7 days. The structures of the prepared compounds were investigated by IR, (1)H-NMR and MALDI-TOF mass spectroscopy. |
format | Online Article Text |
id | pubmed-6254204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62542042018-11-30 The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives Omran, Omran Abdellah Molecules Article New dissymmetric and asymmetric p-tert-butylthiacalix[4]arene derivatives were prepared as a result of the reaction of p-tert-butylthiacalix[4]arene with diethyl bromomalonate in the presence of different alkali metals (Cs, K and Na) in refluxing acetone for 7 days. The structures of the prepared compounds were investigated by IR, (1)H-NMR and MALDI-TOF mass spectroscopy. Molecular Diversity Preservation International 2009-05-07 /pmc/articles/PMC6254204/ /pubmed/19471195 http://dx.doi.org/10.3390/molecules14051755 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. 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 | Article Omran, Omran Abdellah The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives |
title | The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives |
title_full | The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives |
title_fullStr | The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives |
title_full_unstemmed | The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives |
title_short | The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives |
title_sort | reaction of diethyl bromomalonate with p-tert-butylthia-calix[4]arene: an approach to asymmetrical derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254204/ https://www.ncbi.nlm.nih.gov/pubmed/19471195 http://dx.doi.org/10.3390/molecules14051755 |
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