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Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones

As part of our project devoted to the synthesis of heterocycles including thiazole rings, some new 5-arylidene-2-thioxo-3-N-arylthiazolidin-4-ones were synthesized by Knoevenagel condensation. An interesting feature of these compounds is that their chirality is induced by that of their 3-N-(2-alkylo...

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Detalles Bibliográficos
Autores principales: Toubal, Khaled, Djafri, Ayada, Chouaih, Abdelkader, Talbi, Abdou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268637/
https://www.ncbi.nlm.nih.gov/pubmed/22430117
http://dx.doi.org/10.3390/molecules17033501
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author Toubal, Khaled
Djafri, Ayada
Chouaih, Abdelkader
Talbi, Abdou
author_facet Toubal, Khaled
Djafri, Ayada
Chouaih, Abdelkader
Talbi, Abdou
author_sort Toubal, Khaled
collection PubMed
description As part of our project devoted to the synthesis of heterocycles including thiazole rings, some new 5-arylidene-2-thioxo-3-N-arylthiazolidin-4-ones were synthesized by Knoevenagel condensation. An interesting feature of these compounds is that their chirality is induced by that of their 3-N-(2-alkyloxyaryl)-2-thioxothiazolidin-4-one precursors, which in turn is due to the presence of a C2 axis of chirality. These new compounds were characterized by spectroscopic methods (IR, (1)H-NMR, (13)C-NMR). The structure of compound (Z)-(2g) was further determined by X-ray diffraction.
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spelling pubmed-62686372018-12-20 Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones Toubal, Khaled Djafri, Ayada Chouaih, Abdelkader Talbi, Abdou Molecules Article As part of our project devoted to the synthesis of heterocycles including thiazole rings, some new 5-arylidene-2-thioxo-3-N-arylthiazolidin-4-ones were synthesized by Knoevenagel condensation. An interesting feature of these compounds is that their chirality is induced by that of their 3-N-(2-alkyloxyaryl)-2-thioxothiazolidin-4-one precursors, which in turn is due to the presence of a C2 axis of chirality. These new compounds were characterized by spectroscopic methods (IR, (1)H-NMR, (13)C-NMR). The structure of compound (Z)-(2g) was further determined by X-ray diffraction. MDPI 2012-03-19 /pmc/articles/PMC6268637/ /pubmed/22430117 http://dx.doi.org/10.3390/molecules17033501 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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
Toubal, Khaled
Djafri, Ayada
Chouaih, Abdelkader
Talbi, Abdou
Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
title Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
title_full Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
title_fullStr Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
title_full_unstemmed Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
title_short Synthesis and Structural Determination of Novel 5-Arylidene-3-N(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
title_sort synthesis and structural determination of novel 5-arylidene-3-n(2-alkyloxyaryl)-2-thioxothiazolidin-4-ones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268637/
https://www.ncbi.nlm.nih.gov/pubmed/22430117
http://dx.doi.org/10.3390/molecules17033501
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