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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
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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%). |
format | Online Article Text |
id | pubmed-3876076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
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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