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Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles
We report a method for directed ortho-arylation of N-aryl pyrazoles with arylboronic acids. Reactions proceeded in the presence of a Co(hfacac)(2) catalyst, CeSO(4) oxidant, and HFIP solvent. Functionalities such as nitro, ester, bromo, and ketone groups were compatible with the reaction conditions....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695287/ https://www.ncbi.nlm.nih.gov/pubmed/35423432 http://dx.doi.org/10.1039/d1ra00975c |
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author | Nguyen, Tung T. Le, Lam V. Pham, Hai H. Nguyen, Dung H. Phan, Nam T. S. Le, Ha V. Phan, Anh N. Q. |
author_facet | Nguyen, Tung T. Le, Lam V. Pham, Hai H. Nguyen, Dung H. Phan, Nam T. S. Le, Ha V. Phan, Anh N. Q. |
author_sort | Nguyen, Tung T. |
collection | PubMed |
description | We report a method for directed ortho-arylation of N-aryl pyrazoles with arylboronic acids. Reactions proceeded in the presence of a Co(hfacac)(2) catalyst, CeSO(4) oxidant, and HFIP solvent. Functionalities such as nitro, ester, bromo, and ketone groups were compatible with the reaction conditions. Using heterocycles including thiophene and carbazole was also feasible. |
format | Online Article Text |
id | pubmed-8695287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86952872022-04-13 Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles Nguyen, Tung T. Le, Lam V. Pham, Hai H. Nguyen, Dung H. Phan, Nam T. S. Le, Ha V. Phan, Anh N. Q. RSC Adv Chemistry We report a method for directed ortho-arylation of N-aryl pyrazoles with arylboronic acids. Reactions proceeded in the presence of a Co(hfacac)(2) catalyst, CeSO(4) oxidant, and HFIP solvent. Functionalities such as nitro, ester, bromo, and ketone groups were compatible with the reaction conditions. Using heterocycles including thiophene and carbazole was also feasible. The Royal Society of Chemistry 2021-03-01 /pmc/articles/PMC8695287/ /pubmed/35423432 http://dx.doi.org/10.1039/d1ra00975c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Nguyen, Tung T. Le, Lam V. Pham, Hai H. Nguyen, Dung H. Phan, Nam T. S. Le, Ha V. Phan, Anh N. Q. Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles |
title | Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles |
title_full | Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles |
title_fullStr | Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles |
title_full_unstemmed | Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles |
title_short | Cobalt-catalyzed, directed arylation of C–H bonds in N-aryl pyrazoles |
title_sort | cobalt-catalyzed, directed arylation of c–h bonds in n-aryl pyrazoles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695287/ https://www.ncbi.nlm.nih.gov/pubmed/35423432 http://dx.doi.org/10.1039/d1ra00975c |
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