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A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation
The presented study is the first report of the synthesis of terpyridines in the presence of a nanomagnetic catalyst instead of harmful reagents. Herein, Fe(3)O(4)@O(2)PO(2)(CH(2))(2)NH(3)(+)CF(3)CO(2)(−) as a retrievable nanocatalyst with magnetic properties was applied for the multi-component react...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055316/ https://www.ncbi.nlm.nih.gov/pubmed/35518593 http://dx.doi.org/10.1039/d0ra04461j |
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author | Karimi, Fatemeh Yarie, Meysam Zolfigol, Mohammad Ali |
author_facet | Karimi, Fatemeh Yarie, Meysam Zolfigol, Mohammad Ali |
author_sort | Karimi, Fatemeh |
collection | PubMed |
description | The presented study is the first report of the synthesis of terpyridines in the presence of a nanomagnetic catalyst instead of harmful reagents. Herein, Fe(3)O(4)@O(2)PO(2)(CH(2))(2)NH(3)(+)CF(3)CO(2)(−) as a retrievable nanocatalyst with magnetic properties was applied for the multi-component reaction between acetylpyridine derivatives (2 or 3 or 4-isomer), aryl aldehydes and ammonium acetate under conventional heating conditions in the absence of any solvent. The derived terpyridines were obtained with acceptable yields and brief reaction times via a cooperative vinylogous anomeric based oxidation route. Fe(3)O(4)@O(2)PO(2)(CH(2))(2)NH(3)(+)CF(3)CO(2)(−) showed a high capability for recovery and reuse in the mentioned reaction. |
format | Online Article Text |
id | pubmed-9055316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90553162022-05-04 A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation Karimi, Fatemeh Yarie, Meysam Zolfigol, Mohammad Ali RSC Adv Chemistry The presented study is the first report of the synthesis of terpyridines in the presence of a nanomagnetic catalyst instead of harmful reagents. Herein, Fe(3)O(4)@O(2)PO(2)(CH(2))(2)NH(3)(+)CF(3)CO(2)(−) as a retrievable nanocatalyst with magnetic properties was applied for the multi-component reaction between acetylpyridine derivatives (2 or 3 or 4-isomer), aryl aldehydes and ammonium acetate under conventional heating conditions in the absence of any solvent. The derived terpyridines were obtained with acceptable yields and brief reaction times via a cooperative vinylogous anomeric based oxidation route. Fe(3)O(4)@O(2)PO(2)(CH(2))(2)NH(3)(+)CF(3)CO(2)(−) showed a high capability for recovery and reuse in the mentioned reaction. The Royal Society of Chemistry 2020-07-08 /pmc/articles/PMC9055316/ /pubmed/35518593 http://dx.doi.org/10.1039/d0ra04461j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Karimi, Fatemeh Yarie, Meysam Zolfigol, Mohammad Ali A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
title | A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
title_full | A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
title_fullStr | A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
title_full_unstemmed | A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
title_short | A convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
title_sort | convenient method for synthesis of terpyridines via a cooperative vinylogous anomeric based oxidation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055316/ https://www.ncbi.nlm.nih.gov/pubmed/35518593 http://dx.doi.org/10.1039/d0ra04461j |
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