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An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water
An efficient and green synthesis of 4-ferrocenylquinoline derivatives through a TsOH-catalyzed three-component reaction of aromatic aldehydes, amines and ferrocenylacetylene in water has been successfully developed. This strategy is a powerful method for the construction of diverse ferrocenyl-quinol...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078733/ https://www.ncbi.nlm.nih.gov/pubmed/35541872 http://dx.doi.org/10.1039/c8ra01004h |
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author | Mou, Rui-Qi Zhao, Mei Lv, Xue-Xin Zhang, Sheng-Yan Guo, Dian-Shun |
author_facet | Mou, Rui-Qi Zhao, Mei Lv, Xue-Xin Zhang, Sheng-Yan Guo, Dian-Shun |
author_sort | Mou, Rui-Qi |
collection | PubMed |
description | An efficient and green synthesis of 4-ferrocenylquinoline derivatives through a TsOH-catalyzed three-component reaction of aromatic aldehydes, amines and ferrocenylacetylene in water has been successfully developed. This strategy is a powerful method for the construction of diverse ferrocenyl-quinoline conjugates from simple available starting materials as it minimized the use of metal catalyst and organic solvent in the reaction process. The conjugates feature unique structures and excellent electronic properties. Moreover, a plausible mechanism for this TsOH-catalyzed three-component reaction was proposed and assessed. |
format | Online Article Text |
id | pubmed-9078733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90787332022-05-09 An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water Mou, Rui-Qi Zhao, Mei Lv, Xue-Xin Zhang, Sheng-Yan Guo, Dian-Shun RSC Adv Chemistry An efficient and green synthesis of 4-ferrocenylquinoline derivatives through a TsOH-catalyzed three-component reaction of aromatic aldehydes, amines and ferrocenylacetylene in water has been successfully developed. This strategy is a powerful method for the construction of diverse ferrocenyl-quinoline conjugates from simple available starting materials as it minimized the use of metal catalyst and organic solvent in the reaction process. The conjugates feature unique structures and excellent electronic properties. Moreover, a plausible mechanism for this TsOH-catalyzed three-component reaction was proposed and assessed. The Royal Society of Chemistry 2018-03-06 /pmc/articles/PMC9078733/ /pubmed/35541872 http://dx.doi.org/10.1039/c8ra01004h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Mou, Rui-Qi Zhao, Mei Lv, Xue-Xin Zhang, Sheng-Yan Guo, Dian-Shun An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water |
title | An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water |
title_full | An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water |
title_fullStr | An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water |
title_full_unstemmed | An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water |
title_short | An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water |
title_sort | efficient and green synthesis of ferrocenyl-quinoline conjugates via a tsoh-catalyzed three-component reaction in water |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078733/ https://www.ncbi.nlm.nih.gov/pubmed/35541872 http://dx.doi.org/10.1039/c8ra01004h |
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