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Application of Nanomagnetic Metal–Organic Frameworks in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous Anomeric-Based Oxidation
[Image: see text] In the current study, we synthesized a new nanomagnetic metal–organic framework Fe(3)O(4)@MIL-53(Al)-N(CH(2)PO(3))(2) and characterized it using various techniques. This nanomagnetic metal–organic framework was used for the synthesis of a wide range of nicotinonitrile derivatives a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233831/ https://www.ncbi.nlm.nih.gov/pubmed/37273641 http://dx.doi.org/10.1021/acsomega.2c06651 |
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author | Danishyar, Bashirullah Sepehrmansourie, Hassan Ahmadi, Hossein Zarei, Mahmoud Zolfigol, Mohammad Ali Hosseinifard, Mojtaba |
author_facet | Danishyar, Bashirullah Sepehrmansourie, Hassan Ahmadi, Hossein Zarei, Mahmoud Zolfigol, Mohammad Ali Hosseinifard, Mojtaba |
author_sort | Danishyar, Bashirullah |
collection | PubMed |
description | [Image: see text] In the current study, we synthesized a new nanomagnetic metal–organic framework Fe(3)O(4)@MIL-53(Al)-N(CH(2)PO(3))(2) and characterized it using various techniques. This nanomagnetic metal–organic framework was used for the synthesis of a wide range of nicotinonitrile derivatives as suitable drug candidates by a four-component reaction of 3-oxo-3-phenylpropanenitrile or 3-(4-chlorophenyl)-3-oxopropanenitrile, ammonium acetate (NH(4)OAc), acetophenone derivatives, and various aldehydes including those bearing electron-donating, electron-withdrawing, and halogen groups, which afforded desired products (27 samples) via a cooperative vinylogous anomeric-based oxidation (CVABO) mechanism under solvent-free conditions in excellent yields (68–90%) and short reaction times (40–60 min). Increasing the surface-to-volume ratio, easy separation of the catalyst using an external magnet, and high chemical and temperature stability are the advantages of the described nanomagnetic metal–organic frameworks. |
format | Online Article Text |
id | pubmed-10233831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102338312023-06-02 Application of Nanomagnetic Metal–Organic Frameworks in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous Anomeric-Based Oxidation Danishyar, Bashirullah Sepehrmansourie, Hassan Ahmadi, Hossein Zarei, Mahmoud Zolfigol, Mohammad Ali Hosseinifard, Mojtaba ACS Omega [Image: see text] In the current study, we synthesized a new nanomagnetic metal–organic framework Fe(3)O(4)@MIL-53(Al)-N(CH(2)PO(3))(2) and characterized it using various techniques. This nanomagnetic metal–organic framework was used for the synthesis of a wide range of nicotinonitrile derivatives as suitable drug candidates by a four-component reaction of 3-oxo-3-phenylpropanenitrile or 3-(4-chlorophenyl)-3-oxopropanenitrile, ammonium acetate (NH(4)OAc), acetophenone derivatives, and various aldehydes including those bearing electron-donating, electron-withdrawing, and halogen groups, which afforded desired products (27 samples) via a cooperative vinylogous anomeric-based oxidation (CVABO) mechanism under solvent-free conditions in excellent yields (68–90%) and short reaction times (40–60 min). Increasing the surface-to-volume ratio, easy separation of the catalyst using an external magnet, and high chemical and temperature stability are the advantages of the described nanomagnetic metal–organic frameworks. American Chemical Society 2023-05-17 /pmc/articles/PMC10233831/ /pubmed/37273641 http://dx.doi.org/10.1021/acsomega.2c06651 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Danishyar, Bashirullah Sepehrmansourie, Hassan Ahmadi, Hossein Zarei, Mahmoud Zolfigol, Mohammad Ali Hosseinifard, Mojtaba Application of Nanomagnetic Metal–Organic Frameworks in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous Anomeric-Based Oxidation |
title | Application of
Nanomagnetic Metal–Organic Frameworks
in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous
Anomeric-Based Oxidation |
title_full | Application of
Nanomagnetic Metal–Organic Frameworks
in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous
Anomeric-Based Oxidation |
title_fullStr | Application of
Nanomagnetic Metal–Organic Frameworks
in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous
Anomeric-Based Oxidation |
title_full_unstemmed | Application of
Nanomagnetic Metal–Organic Frameworks
in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous
Anomeric-Based Oxidation |
title_short | Application of
Nanomagnetic Metal–Organic Frameworks
in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous
Anomeric-Based Oxidation |
title_sort | application of
nanomagnetic metal–organic frameworks
in the green synthesis of nicotinonitriles via cooperative vinylogous
anomeric-based oxidation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233831/ https://www.ncbi.nlm.nih.gov/pubmed/37273641 http://dx.doi.org/10.1021/acsomega.2c06651 |
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