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Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst
Synthesis of 3,4-dihydropyrimidin-2(1H)-one and 3,4-dihydropyrimidin-2(1H)-thione derivatives from aldehydes, 1,3-dicarbonyl derivatives and urea or thiourea using granite and quartz as new, natural and reusable catalysts. Some of the 3,4-dihydropyrimidin-2(1H)-thione derivatives were used to prepar...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765801/ https://www.ncbi.nlm.nih.gov/pubmed/24052868 http://dx.doi.org/10.1155/2013/706437 |
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author | Elmaghraby, A. M. Mousa, I. A. Harb, A. A. Mahgoub, M. Y. |
author_facet | Elmaghraby, A. M. Mousa, I. A. Harb, A. A. Mahgoub, M. Y. |
author_sort | Elmaghraby, A. M. |
collection | PubMed |
description | Synthesis of 3,4-dihydropyrimidin-2(1H)-one and 3,4-dihydropyrimidin-2(1H)-thione derivatives from aldehydes, 1,3-dicarbonyl derivatives and urea or thiourea using granite and quartz as new, natural and reusable catalysts. Some of the 3,4-dihydropyrimidin-2(1H)-thione derivatives were used to prepare new heterocyclic compounds. The antimicrobial activity of selected examples of the synthesized compounds was tested and showed moderate activity. |
format | Online Article Text |
id | pubmed-3765801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37658012013-09-19 Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst Elmaghraby, A. M. Mousa, I. A. Harb, A. A. Mahgoub, M. Y. ISRN Org Chem Research Article Synthesis of 3,4-dihydropyrimidin-2(1H)-one and 3,4-dihydropyrimidin-2(1H)-thione derivatives from aldehydes, 1,3-dicarbonyl derivatives and urea or thiourea using granite and quartz as new, natural and reusable catalysts. Some of the 3,4-dihydropyrimidin-2(1H)-thione derivatives were used to prepare new heterocyclic compounds. The antimicrobial activity of selected examples of the synthesized compounds was tested and showed moderate activity. Hindawi Publishing Corporation 2013-08-18 /pmc/articles/PMC3765801/ /pubmed/24052868 http://dx.doi.org/10.1155/2013/706437 Text en Copyright © 2013 A. M. Elmaghraby et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Elmaghraby, A. M. Mousa, I. A. Harb, A. A. Mahgoub, M. Y. Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst |
title | Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst |
title_full | Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst |
title_fullStr | Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst |
title_full_unstemmed | Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst |
title_short | Three Component Reaction: An Efficient Synthesis and Reactions of 3,4-Dihydropyrimidin-2(1H)-Ones and Thiones Using New Natural Catalyst |
title_sort | three component reaction: an efficient synthesis and reactions of 3,4-dihydropyrimidin-2(1h)-ones and thiones using new natural catalyst |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765801/ https://www.ncbi.nlm.nih.gov/pubmed/24052868 http://dx.doi.org/10.1155/2013/706437 |
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