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Ionically Tagged Magnetic Nanoparticles with Urea Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic Acids via an Anomeric-Based Oxidation Mechanism
[Image: see text] In this exploration, we reported the design and synthesis of a novel ionically tagged magnetic nanoparticles bearing urea linkers, namely, Fe(3)O(4)@SiO(2)@(CH(2))(3)–urea–thiazole sulfonic acid chloride. The structure of the mentioned compound was fully characterized by using seve...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045317/ https://www.ncbi.nlm.nih.gov/pubmed/32118136 http://dx.doi.org/10.1021/acsomega.9b03277 |
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author | Ghasemi, Parvin Yarie, Meysam Zolfigol, Mohammad Ali Taherpour, Avat Arman Torabi, Morteza |
author_facet | Ghasemi, Parvin Yarie, Meysam Zolfigol, Mohammad Ali Taherpour, Avat Arman Torabi, Morteza |
author_sort | Ghasemi, Parvin |
collection | PubMed |
description | [Image: see text] In this exploration, we reported the design and synthesis of a novel ionically tagged magnetic nanoparticles bearing urea linkers, namely, Fe(3)O(4)@SiO(2)@(CH(2))(3)–urea–thiazole sulfonic acid chloride. The structure of the mentioned compound was fully characterized by using several techniques including Fourier transform infrared spectroscopy, energy-dispersive X-ray analysis, elemental mapping analysis, thermogravimetric analysis/differential thermal analysis, scanning electron microscopy, transmission electron microscopy, and vibrating sample magnetometer. In the presence of the novel reusable catalyst, applied starting materials including aryl aldehydes, pyruvic acid, and 1-naphthylamine condensed to afford the desired 2-aryl-quinoline-4-carboxylic acid derivatives via an anomeric-based oxidation pathway under solvent-free conditions. |
format | Online Article Text |
id | pubmed-7045317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70453172020-02-28 Ionically Tagged Magnetic Nanoparticles with Urea Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic Acids via an Anomeric-Based Oxidation Mechanism Ghasemi, Parvin Yarie, Meysam Zolfigol, Mohammad Ali Taherpour, Avat Arman Torabi, Morteza ACS Omega [Image: see text] In this exploration, we reported the design and synthesis of a novel ionically tagged magnetic nanoparticles bearing urea linkers, namely, Fe(3)O(4)@SiO(2)@(CH(2))(3)–urea–thiazole sulfonic acid chloride. The structure of the mentioned compound was fully characterized by using several techniques including Fourier transform infrared spectroscopy, energy-dispersive X-ray analysis, elemental mapping analysis, thermogravimetric analysis/differential thermal analysis, scanning electron microscopy, transmission electron microscopy, and vibrating sample magnetometer. In the presence of the novel reusable catalyst, applied starting materials including aryl aldehydes, pyruvic acid, and 1-naphthylamine condensed to afford the desired 2-aryl-quinoline-4-carboxylic acid derivatives via an anomeric-based oxidation pathway under solvent-free conditions. American Chemical Society 2020-02-11 /pmc/articles/PMC7045317/ /pubmed/32118136 http://dx.doi.org/10.1021/acsomega.9b03277 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Ghasemi, Parvin Yarie, Meysam Zolfigol, Mohammad Ali Taherpour, Avat Arman Torabi, Morteza Ionically Tagged Magnetic Nanoparticles with Urea Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic Acids via an Anomeric-Based Oxidation Mechanism |
title | Ionically Tagged Magnetic Nanoparticles with Urea
Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic
Acids via an Anomeric-Based Oxidation Mechanism |
title_full | Ionically Tagged Magnetic Nanoparticles with Urea
Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic
Acids via an Anomeric-Based Oxidation Mechanism |
title_fullStr | Ionically Tagged Magnetic Nanoparticles with Urea
Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic
Acids via an Anomeric-Based Oxidation Mechanism |
title_full_unstemmed | Ionically Tagged Magnetic Nanoparticles with Urea
Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic
Acids via an Anomeric-Based Oxidation Mechanism |
title_short | Ionically Tagged Magnetic Nanoparticles with Urea
Linkers: Application for Preparation of 2-Aryl-quinoline-4-carboxylic
Acids via an Anomeric-Based Oxidation Mechanism |
title_sort | ionically tagged magnetic nanoparticles with urea
linkers: application for preparation of 2-aryl-quinoline-4-carboxylic
acids via an anomeric-based oxidation mechanism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045317/ https://www.ncbi.nlm.nih.gov/pubmed/32118136 http://dx.doi.org/10.1021/acsomega.9b03277 |
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