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Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst

In this project, Sn(II)/nano silica has been prepared using a simple deposition of SnCl(2).2.H(2)O on nano-silica. The prepared catalyst has been used as a green and reusable catalyst for synthesis of 14H-dibenzoxanthenes through a one-pot condensation reaction of β-naphthol with various aliphatic a...

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Detalles Bibliográficos
Autores principales: Tavakol, Hossein, Firouzi, Mahdieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666768/
https://www.ncbi.nlm.nih.gov/pubmed/36405309
http://dx.doi.org/10.3389/fchem.2022.1015830
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author Tavakol, Hossein
Firouzi, Mahdieh
author_facet Tavakol, Hossein
Firouzi, Mahdieh
author_sort Tavakol, Hossein
collection PubMed
description In this project, Sn(II)/nano silica has been prepared using a simple deposition of SnCl(2).2.H(2)O on nano-silica. The prepared catalyst has been used as a green and reusable catalyst for synthesis of 14H-dibenzoxanthenes through a one-pot condensation reaction of β-naphthol with various aliphatic and aromatic aldehydes. Several xanthene derivatives have been synthesized using ethanol as the solvent, 10 mol percent of the catalyst, at reflux condition, in 3 h, and by 48%–94% yield. The structures of the synthesized derivatives are confirmed by melting point, FT-IR, (13)C-NMR, and (1)H-NMR analyses. Additionally, the nanocatalyst composition was confirmed by SEM, EDX, FT-IR, and XRD.
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spelling pubmed-96667682022-11-17 Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst Tavakol, Hossein Firouzi, Mahdieh Front Chem Chemistry In this project, Sn(II)/nano silica has been prepared using a simple deposition of SnCl(2).2.H(2)O on nano-silica. The prepared catalyst has been used as a green and reusable catalyst for synthesis of 14H-dibenzoxanthenes through a one-pot condensation reaction of β-naphthol with various aliphatic and aromatic aldehydes. Several xanthene derivatives have been synthesized using ethanol as the solvent, 10 mol percent of the catalyst, at reflux condition, in 3 h, and by 48%–94% yield. The structures of the synthesized derivatives are confirmed by melting point, FT-IR, (13)C-NMR, and (1)H-NMR analyses. Additionally, the nanocatalyst composition was confirmed by SEM, EDX, FT-IR, and XRD. Frontiers Media S.A. 2022-11-02 /pmc/articles/PMC9666768/ /pubmed/36405309 http://dx.doi.org/10.3389/fchem.2022.1015830 Text en Copyright © 2022 Tavakol and Firouzi. 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
Tavakol, Hossein
Firouzi, Mahdieh
Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst
title Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst
title_full Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst
title_fullStr Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst
title_full_unstemmed Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst
title_short Synthesis of 14H-dibenzoxanthenes in green media using Sn(II)/nano silica as an efficient catalyst
title_sort synthesis of 14h-dibenzoxanthenes in green media using sn(ii)/nano silica as an efficient catalyst
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666768/
https://www.ncbi.nlm.nih.gov/pubmed/36405309
http://dx.doi.org/10.3389/fchem.2022.1015830
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