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An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction
Various novel pyrano [2,3-d]pyrimidines 5 and furopyrano [2,3-d]pyrimidines 7 were synthesized in 80–99% yields via a multicomponent domino Knoevenagel/hetero-Diels-Alder reaction of 1,3-dimethyl barbituric acid with an aromatic aldehyde and ethyl vinyl ether/2,3-dihydrofuran in presence of 1 mol% o...
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1525172/ https://www.ncbi.nlm.nih.gov/pubmed/16768808 http://dx.doi.org/10.1186/1860-5397-2-11 |
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author | Prajapati, Dipak Gohain, Mukut |
author_facet | Prajapati, Dipak Gohain, Mukut |
author_sort | Prajapati, Dipak |
collection | PubMed |
description | Various novel pyrano [2,3-d]pyrimidines 5 and furopyrano [2,3-d]pyrimidines 7 were synthesized in 80–99% yields via a multicomponent domino Knoevenagel/hetero-Diels-Alder reaction of 1,3-dimethyl barbituric acid with an aromatic aldehyde and ethyl vinyl ether/2,3-dihydrofuran in presence of 1 mol% of indium(III) chloride. The reaction also proceeds in aqueous media without using any catalyst, but the yield is comparatively less (65–70%). |
format | Text |
id | pubmed-1525172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-15251722006-08-02 An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction Prajapati, Dipak Gohain, Mukut Beilstein J Org Chem Full Research Paper Various novel pyrano [2,3-d]pyrimidines 5 and furopyrano [2,3-d]pyrimidines 7 were synthesized in 80–99% yields via a multicomponent domino Knoevenagel/hetero-Diels-Alder reaction of 1,3-dimethyl barbituric acid with an aromatic aldehyde and ethyl vinyl ether/2,3-dihydrofuran in presence of 1 mol% of indium(III) chloride. The reaction also proceeds in aqueous media without using any catalyst, but the yield is comparatively less (65–70%). Beilstein-Institut 2006-06-13 /pmc/articles/PMC1525172/ /pubmed/16768808 http://dx.doi.org/10.1186/1860-5397-2-11 Text en Copyright © 2006, Prajapati and Gohain https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Prajapati, Dipak Gohain, Mukut An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
title | An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
title_full | An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
title_fullStr | An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
title_full_unstemmed | An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
title_short | An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
title_sort | efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium-catalyzed multi-component domino reaction |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1525172/ https://www.ncbi.nlm.nih.gov/pubmed/16768808 http://dx.doi.org/10.1186/1860-5397-2-11 |
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