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Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives
Application of a dynamic microwave power system in the chemical synthesis of some phenothiazine and quinoline derivatives is described. Heterocyclic ring formation, aromatic nucleophilic substitution and heterocyclic aldehydes/ketones condensation reactions were performed on solid support, or under...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666047/ |
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author | Găină, Luiza Cristea, Castelia Moldovan, Claudia Porumb, Dan Surducan, Emanoil Deleanu, Călin Mahamoud, Abdalah Barbe, Jacques Silberg, Ioan A. |
author_facet | Găină, Luiza Cristea, Castelia Moldovan, Claudia Porumb, Dan Surducan, Emanoil Deleanu, Călin Mahamoud, Abdalah Barbe, Jacques Silberg, Ioan A. |
author_sort | Găină, Luiza |
collection | PubMed |
description | Application of a dynamic microwave power system in the chemical synthesis of some phenothiazine and quinoline derivatives is described. Heterocyclic ring formation, aromatic nucleophilic substitution and heterocyclic aldehydes/ketones condensation reactions were performed on solid support, or under solvent free reaction conditions. The microwave-assisted Duff formylation of phenothiazine was achieved. Comparison of microwave-assisted synthesis with the conventional synthetic methods demonstrates advantages related to shorter reaction times and in some cases better reaction yields. |
format | Online Article Text |
id | pubmed-3666047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-36660472013-05-30 Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives Găină, Luiza Cristea, Castelia Moldovan, Claudia Porumb, Dan Surducan, Emanoil Deleanu, Călin Mahamoud, Abdalah Barbe, Jacques Silberg, Ioan A. Int J Mol Sci Articles Application of a dynamic microwave power system in the chemical synthesis of some phenothiazine and quinoline derivatives is described. Heterocyclic ring formation, aromatic nucleophilic substitution and heterocyclic aldehydes/ketones condensation reactions were performed on solid support, or under solvent free reaction conditions. The microwave-assisted Duff formylation of phenothiazine was achieved. Comparison of microwave-assisted synthesis with the conventional synthetic methods demonstrates advantages related to shorter reaction times and in some cases better reaction yields. Molecular Diversity Preservation International (MDPI) 2007-02-13 /pmc/articles/PMC3666047/ Text en © 2007 by MDPI Reproduction is permitted for noncommercial purposes. |
spellingShingle | Articles Găină, Luiza Cristea, Castelia Moldovan, Claudia Porumb, Dan Surducan, Emanoil Deleanu, Călin Mahamoud, Abdalah Barbe, Jacques Silberg, Ioan A. Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives |
title | Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives |
title_full | Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives |
title_fullStr | Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives |
title_full_unstemmed | Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives |
title_short | Microwave-Assisted Synthesis of Phenothiazine and Quinoline Derivatives |
title_sort | microwave-assisted synthesis of phenothiazine and quinoline derivatives |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666047/ |
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