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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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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. |
format | Online Article Text |
id | pubmed-6268637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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