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FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction
ABSTRACT: FeNH(4)(SO(4))(2)·12H(2)O (alum) efficiently catalyzes the one-pot three-component reaction of dimedone, aldehydes, and 3-aminocrotonate to afford 1,4-dihydropyridines. The work-up is easy, and the products are obtained in good to excellent yields and high purity. GRAPHICAL ABSTRACT: [Imag...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495042/ https://www.ncbi.nlm.nih.gov/pubmed/26166866 http://dx.doi.org/10.1007/s00706-011-0672-6 |
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author | Mohammadi, Ali A. Hadadzahmatkesh, Armin Asghariganjeh, Mohammad R. |
author_facet | Mohammadi, Ali A. Hadadzahmatkesh, Armin Asghariganjeh, Mohammad R. |
author_sort | Mohammadi, Ali A. |
collection | PubMed |
description | ABSTRACT: FeNH(4)(SO(4))(2)·12H(2)O (alum) efficiently catalyzes the one-pot three-component reaction of dimedone, aldehydes, and 3-aminocrotonate to afford 1,4-dihydropyridines. The work-up is easy, and the products are obtained in good to excellent yields and high purity. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-4495042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-44950422015-07-09 FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction Mohammadi, Ali A. Hadadzahmatkesh, Armin Asghariganjeh, Mohammad R. Monatsh Chem Original Paper ABSTRACT: FeNH(4)(SO(4))(2)·12H(2)O (alum) efficiently catalyzes the one-pot three-component reaction of dimedone, aldehydes, and 3-aminocrotonate to afford 1,4-dihydropyridines. The work-up is easy, and the products are obtained in good to excellent yields and high purity. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2011-11-17 2012 /pmc/articles/PMC4495042/ /pubmed/26166866 http://dx.doi.org/10.1007/s00706-011-0672-6 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Paper Mohammadi, Ali A. Hadadzahmatkesh, Armin Asghariganjeh, Mohammad R. FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction |
title | FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction |
title_full | FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction |
title_fullStr | FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction |
title_full_unstemmed | FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction |
title_short | FeNH(4)(SO(4))(2)·12H(2)O (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the Hantzsch reaction |
title_sort | fenh(4)(so(4))(2)·12h(2)o (alum)-catalyzed preparation of 1,4-dihydropyridines: improved conditions for the hantzsch reaction |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495042/ https://www.ncbi.nlm.nih.gov/pubmed/26166866 http://dx.doi.org/10.1007/s00706-011-0672-6 |
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