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Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions
We have found that dodecatungstophosphoric acid (H(3)PW(12)O(40)), samarium or ruthenium(ΙΙΙ) chloride act as efficient catalysts for the synthesis of unsaturated 2-phenyl-5(4H)oxazolone derivatives under solvent-free conditions. The key features of the reported protocols are short reaction times, h...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245382/ https://www.ncbi.nlm.nih.gov/pubmed/19104489 http://dx.doi.org/10.3390/molecules13123246 |
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author | Tikdari, Ahmad Momeni Fozooni, Samieh Hamidian, Hooshang |
author_facet | Tikdari, Ahmad Momeni Fozooni, Samieh Hamidian, Hooshang |
author_sort | Tikdari, Ahmad Momeni |
collection | PubMed |
description | We have found that dodecatungstophosphoric acid (H(3)PW(12)O(40)), samarium or ruthenium(ΙΙΙ) chloride act as efficient catalysts for the synthesis of unsaturated 2-phenyl-5(4H)oxazolone derivatives under solvent-free conditions. The key features of the reported protocols are short reaction times, high yields of products under ambient conditions and simple workups. |
format | Online Article Text |
id | pubmed-6245382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62453822018-11-26 Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions Tikdari, Ahmad Momeni Fozooni, Samieh Hamidian, Hooshang Molecules Article We have found that dodecatungstophosphoric acid (H(3)PW(12)O(40)), samarium or ruthenium(ΙΙΙ) chloride act as efficient catalysts for the synthesis of unsaturated 2-phenyl-5(4H)oxazolone derivatives under solvent-free conditions. The key features of the reported protocols are short reaction times, high yields of products under ambient conditions and simple workups. MDPI 2008-12-18 /pmc/articles/PMC6245382/ /pubmed/19104489 http://dx.doi.org/10.3390/molecules13123246 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. 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 Tikdari, Ahmad Momeni Fozooni, Samieh Hamidian, Hooshang Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions |
title | Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions |
title_full | Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions |
title_fullStr | Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions |
title_full_unstemmed | Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions |
title_short | Dodecatungstophosphoric Acid (H(3)PW(12)O(40)), Samarium and Ruthenium (ІІІ) Chloride Catalyzed Synthesis of Unsaturated 2-Phenyl-5(4H)-oxazolone Derivatives under Solvent-free Conditions |
title_sort | dodecatungstophosphoric acid (h(3)pw(12)o(40)), samarium and ruthenium (ііі) chloride catalyzed synthesis of unsaturated 2-phenyl-5(4h)-oxazolone derivatives under solvent-free conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245382/ https://www.ncbi.nlm.nih.gov/pubmed/19104489 http://dx.doi.org/10.3390/molecules13123246 |
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