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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...

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Autores principales: Găină, Luiza, Cristea, Castelia, Moldovan, Claudia, Porumb, Dan, Surducan, Emanoil, Deleanu, Călin, Mahamoud, Abdalah, Barbe, Jacques, Silberg, Ioan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2007
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.
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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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