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Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans
Recent research has been focused on the transition metal-catalyzed reactions. Herein we have developed nickel-catalyzed synthesis of 3-aryl benzofurans from ortho-alkenyl phenols via intramolecular dehydrogenative coupling. Notably, simple O(2) gas served as an oxidant, without using any sacrificial...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054549/ https://www.ncbi.nlm.nih.gov/pubmed/35516592 http://dx.doi.org/10.1039/d0ra03071f |
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author | Aggarwal, Sakshi Srinivas, Dasari Sreenivasulu, Chinnabattigalla Satyanarayana, Gedu |
author_facet | Aggarwal, Sakshi Srinivas, Dasari Sreenivasulu, Chinnabattigalla Satyanarayana, Gedu |
author_sort | Aggarwal, Sakshi |
collection | PubMed |
description | Recent research has been focused on the transition metal-catalyzed reactions. Herein we have developed nickel-catalyzed synthesis of 3-aryl benzofurans from ortho-alkenyl phenols via intramolecular dehydrogenative coupling. Notably, simple O(2) gas served as an oxidant, without using any sacrificial hydrogen acceptor. The strategy enabled the synthesis of 3-aryl benzofurans in good to excellent yields. |
format | Online Article Text |
id | pubmed-9054549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90545492022-05-04 Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans Aggarwal, Sakshi Srinivas, Dasari Sreenivasulu, Chinnabattigalla Satyanarayana, Gedu RSC Adv Chemistry Recent research has been focused on the transition metal-catalyzed reactions. Herein we have developed nickel-catalyzed synthesis of 3-aryl benzofurans from ortho-alkenyl phenols via intramolecular dehydrogenative coupling. Notably, simple O(2) gas served as an oxidant, without using any sacrificial hydrogen acceptor. The strategy enabled the synthesis of 3-aryl benzofurans in good to excellent yields. The Royal Society of Chemistry 2020-06-10 /pmc/articles/PMC9054549/ /pubmed/35516592 http://dx.doi.org/10.1039/d0ra03071f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Aggarwal, Sakshi Srinivas, Dasari Sreenivasulu, Chinnabattigalla Satyanarayana, Gedu Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
title | Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
title_full | Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
title_fullStr | Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
title_full_unstemmed | Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
title_short | Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
title_sort | nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054549/ https://www.ncbi.nlm.nih.gov/pubmed/35516592 http://dx.doi.org/10.1039/d0ra03071f |
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