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Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives

A simple protocol, involving the green synthesis for the construction of novel bis-pyrimidine derivatives, 3a–i and 4a–e are accomplished by the aqueous diethylamine media promoted tandem Aldol-Michael reaction between two molecules of barbituric acid derivatives 1a,b with various aldehydes. This ef...

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Autores principales: Al-Majid, Abdullah M., Barakat, Assem, AL-Najjar, Hany J., Mabkhot, Yahia N., Ghabbour, Hazem A., Fun, Hoong-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876076/
https://www.ncbi.nlm.nih.gov/pubmed/24317435
http://dx.doi.org/10.3390/ijms141223762
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author Al-Majid, Abdullah M.
Barakat, Assem
AL-Najjar, Hany J.
Mabkhot, Yahia N.
Ghabbour, Hazem A.
Fun, Hoong-Kun
author_facet Al-Majid, Abdullah M.
Barakat, Assem
AL-Najjar, Hany J.
Mabkhot, Yahia N.
Ghabbour, Hazem A.
Fun, Hoong-Kun
author_sort Al-Majid, Abdullah M.
collection PubMed
description A simple protocol, involving the green synthesis for the construction of novel bis-pyrimidine derivatives, 3a–i and 4a–e are accomplished by the aqueous diethylamine media promoted tandem Aldol-Michael reaction between two molecules of barbituric acid derivatives 1a,b with various aldehydes. This efficient synthetic protocol using an economic and environmentally friendly reaction media with versatility and shorter reaction time provides bis-pyrimidine derivatives with high yields (88%–99%).
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spelling pubmed-38760762013-12-31 Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives Al-Majid, Abdullah M. Barakat, Assem AL-Najjar, Hany J. Mabkhot, Yahia N. Ghabbour, Hazem A. Fun, Hoong-Kun Int J Mol Sci Article A simple protocol, involving the green synthesis for the construction of novel bis-pyrimidine derivatives, 3a–i and 4a–e are accomplished by the aqueous diethylamine media promoted tandem Aldol-Michael reaction between two molecules of barbituric acid derivatives 1a,b with various aldehydes. This efficient synthetic protocol using an economic and environmentally friendly reaction media with versatility and shorter reaction time provides bis-pyrimidine derivatives with high yields (88%–99%). Molecular Diversity Preservation International (MDPI) 2013-12-05 /pmc/articles/PMC3876076/ /pubmed/24317435 http://dx.doi.org/10.3390/ijms141223762 Text en © 2013 by the authors; licensee MDPI, 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 Article
Al-Majid, Abdullah M.
Barakat, Assem
AL-Najjar, Hany J.
Mabkhot, Yahia N.
Ghabbour, Hazem A.
Fun, Hoong-Kun
Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives
title Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives
title_full Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives
title_fullStr Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives
title_full_unstemmed Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives
title_short Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives
title_sort tandem aldol-michael reactions in aqueous diethylamine medium: a greener and efficient approach to bis-pyrimidine derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876076/
https://www.ncbi.nlm.nih.gov/pubmed/24317435
http://dx.doi.org/10.3390/ijms141223762
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