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Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions
The diaryl ether moiety is not only prevalent in a significant number of natural products and synthetic pharmaceuticals but also widely found in many pesticides, polymers, and ligands. Ullmann-type cross-coupling reactions between phenols and aryl halides are regarded as one of the most important me...
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/PMC9080655/ https://www.ncbi.nlm.nih.gov/pubmed/35539660 http://dx.doi.org/10.1039/c8ra02818d |
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author | Nejati, Kamellia Ahmadi, Sheida Nikpassand, Mohammad Kheirollahi Nezhad, Parvaneh Delir Vessally, Esmail |
author_facet | Nejati, Kamellia Ahmadi, Sheida Nikpassand, Mohammad Kheirollahi Nezhad, Parvaneh Delir Vessally, Esmail |
author_sort | Nejati, Kamellia |
collection | PubMed |
description | The diaryl ether moiety is not only prevalent in a significant number of natural products and synthetic pharmaceuticals but also widely found in many pesticides, polymers, and ligands. Ullmann-type cross-coupling reactions between phenols and aryl halides are regarded as one of the most important methods for the synthesis of this important and versatile structural motif. In recent years, the use of nano-sized metal catalysts in this coupling reaction has attracted a lot of attention because of these catalysts with their high surface-to-volume ratio, high surface energy, and reactive morphology allows for rapid C–O bond formation under mild and ligand-free conditions. In this review we will highlight the power of these catalysts in Ullmann-type C–O cross-coupling reactions. |
format | Online Article Text |
id | pubmed-9080655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90806552022-05-09 Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions Nejati, Kamellia Ahmadi, Sheida Nikpassand, Mohammad Kheirollahi Nezhad, Parvaneh Delir Vessally, Esmail RSC Adv Chemistry The diaryl ether moiety is not only prevalent in a significant number of natural products and synthetic pharmaceuticals but also widely found in many pesticides, polymers, and ligands. Ullmann-type cross-coupling reactions between phenols and aryl halides are regarded as one of the most important methods for the synthesis of this important and versatile structural motif. In recent years, the use of nano-sized metal catalysts in this coupling reaction has attracted a lot of attention because of these catalysts with their high surface-to-volume ratio, high surface energy, and reactive morphology allows for rapid C–O bond formation under mild and ligand-free conditions. In this review we will highlight the power of these catalysts in Ullmann-type C–O cross-coupling reactions. The Royal Society of Chemistry 2018-05-23 /pmc/articles/PMC9080655/ /pubmed/35539660 http://dx.doi.org/10.1039/c8ra02818d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Nejati, Kamellia Ahmadi, Sheida Nikpassand, Mohammad Kheirollahi Nezhad, Parvaneh Delir Vessally, Esmail Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
title | Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
title_full | Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
title_fullStr | Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
title_full_unstemmed | Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
title_short | Diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
title_sort | diaryl ethers synthesis: nano-catalysts in carbon-oxygen cross-coupling reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080655/ https://www.ncbi.nlm.nih.gov/pubmed/35539660 http://dx.doi.org/10.1039/c8ra02818d |
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