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Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation

Petasites hybridus rhizome water extract was used as green media for the preparation of Ag/Fe(3)O(4)/CdO@multi-walled carbon nanotubes magnetic nanocomposites (Ag/Fe(3)O(4)/CdO@MWCNTs MNCs), and its activity was evaluated by using in the one-pot multicomponent reaction of isatins, acetyl chloride, s...

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Autores principales: Hossaini, Zinatossadat, Mohammadi, Marziyeh, Sheikholeslami-Farahani, Fatemeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559721/
https://www.ncbi.nlm.nih.gov/pubmed/36247666
http://dx.doi.org/10.3389/fchem.2022.949205
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author Hossaini, Zinatossadat
Mohammadi, Marziyeh
Sheikholeslami-Farahani, Fatemeh
author_facet Hossaini, Zinatossadat
Mohammadi, Marziyeh
Sheikholeslami-Farahani, Fatemeh
author_sort Hossaini, Zinatossadat
collection PubMed
description Petasites hybridus rhizome water extract was used as green media for the preparation of Ag/Fe(3)O(4)/CdO@multi-walled carbon nanotubes magnetic nanocomposites (Ag/Fe(3)O(4)/CdO@MWCNTs MNCs), and its activity was evaluated by using in the one-pot multicomponent reaction of isatins, acetyl chloride, secondary amines, vinilidene Meldrum’s acid, primary amines, and malononitrile in an aqueous medium at room temperature for the generation of spiropyridoindolepyrrolidine as new derivatives with tremendous output. In addition, organic pollutant reduction of 4-nitrophenol (4-NP) was carried out by generated Ag/Fe(3)O(4)/CdO@MWCNTs in water at room temperature. The results displayed that Ag/Fe(3)O(4)/CdO@MWCNTs were reduced as pollutants of organic compounds in a short time. The synthesized spiropyridoindolepyrrolidine has an NH(2) functional group that has acidic hydrogen and shows high antioxidant ability. Also, the spiropyridoindolepyrrolidine exhibited antimicrobial ability, and the method that is used for this purpose is the disk diffusion method, and two kinds of bacteria, Gram-positive and Gram-negative, were employed for this analysis. Also, to better understand the reaction mechanism density, functional theory-based quantum chemical methods have been applied. For the generation of spiropyridoindolepyrrolidine, the used process has many properties such as reactions with short time, product with good yields, and simple extraction of catalyst from the mixture of reaction.
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spelling pubmed-95597212022-10-14 Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation Hossaini, Zinatossadat Mohammadi, Marziyeh Sheikholeslami-Farahani, Fatemeh Front Chem Chemistry Petasites hybridus rhizome water extract was used as green media for the preparation of Ag/Fe(3)O(4)/CdO@multi-walled carbon nanotubes magnetic nanocomposites (Ag/Fe(3)O(4)/CdO@MWCNTs MNCs), and its activity was evaluated by using in the one-pot multicomponent reaction of isatins, acetyl chloride, secondary amines, vinilidene Meldrum’s acid, primary amines, and malononitrile in an aqueous medium at room temperature for the generation of spiropyridoindolepyrrolidine as new derivatives with tremendous output. In addition, organic pollutant reduction of 4-nitrophenol (4-NP) was carried out by generated Ag/Fe(3)O(4)/CdO@MWCNTs in water at room temperature. The results displayed that Ag/Fe(3)O(4)/CdO@MWCNTs were reduced as pollutants of organic compounds in a short time. The synthesized spiropyridoindolepyrrolidine has an NH(2) functional group that has acidic hydrogen and shows high antioxidant ability. Also, the spiropyridoindolepyrrolidine exhibited antimicrobial ability, and the method that is used for this purpose is the disk diffusion method, and two kinds of bacteria, Gram-positive and Gram-negative, were employed for this analysis. Also, to better understand the reaction mechanism density, functional theory-based quantum chemical methods have been applied. For the generation of spiropyridoindolepyrrolidine, the used process has many properties such as reactions with short time, product with good yields, and simple extraction of catalyst from the mixture of reaction. Frontiers Media S.A. 2022-09-21 /pmc/articles/PMC9559721/ /pubmed/36247666 http://dx.doi.org/10.3389/fchem.2022.949205 Text en Copyright © 2022 Hossaini, Mohammadi and Sheikholeslami-Farahani. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Hossaini, Zinatossadat
Mohammadi, Marziyeh
Sheikholeslami-Farahani, Fatemeh
Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation
title Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation
title_full Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation
title_fullStr Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation
title_full_unstemmed Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation
title_short Six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: A combined experimental and theoretical investigation
title_sort six-component synthesis and biological activity of novel spiropyridoindolepyrrolidine derivatives: a combined experimental and theoretical investigation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559721/
https://www.ncbi.nlm.nih.gov/pubmed/36247666
http://dx.doi.org/10.3389/fchem.2022.949205
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