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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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Detalles Bibliográficos
Autor principal: Omran, Omran Abdellah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
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
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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.
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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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