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Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles
A series of 4-trifluoromethyl pyrazoles have been prepared via the copper-catalyzed cycloaddition of 2-bromo-3,3,3-trifluoropropene with a variety of N-arylsydnone derivatives under mild conditions. This new protocol under optimized reaction conditions [Cu(OTf)(2)/phen, DBU, CH(3)CN, 35 °C] afforded...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072218/ https://www.ncbi.nlm.nih.gov/pubmed/35529353 http://dx.doi.org/10.1039/c9ra07694h |
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author | Lu, Jiaqing Man, Yuning Zhang, Yabin Lin, Bo Lin, Qi Weng, Zhiqiang |
author_facet | Lu, Jiaqing Man, Yuning Zhang, Yabin Lin, Bo Lin, Qi Weng, Zhiqiang |
author_sort | Lu, Jiaqing |
collection | PubMed |
description | A series of 4-trifluoromethyl pyrazoles have been prepared via the copper-catalyzed cycloaddition of 2-bromo-3,3,3-trifluoropropene with a variety of N-arylsydnone derivatives under mild conditions. This new protocol under optimized reaction conditions [Cu(OTf)(2)/phen, DBU, CH(3)CN, 35 °C] afforded 4-trifluoromethyl pyrazoles in moderate to excellent yields with excellent regioselectivity. |
format | Online Article Text |
id | pubmed-9072218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90722182022-05-06 Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles Lu, Jiaqing Man, Yuning Zhang, Yabin Lin, Bo Lin, Qi Weng, Zhiqiang RSC Adv Chemistry A series of 4-trifluoromethyl pyrazoles have been prepared via the copper-catalyzed cycloaddition of 2-bromo-3,3,3-trifluoropropene with a variety of N-arylsydnone derivatives under mild conditions. This new protocol under optimized reaction conditions [Cu(OTf)(2)/phen, DBU, CH(3)CN, 35 °C] afforded 4-trifluoromethyl pyrazoles in moderate to excellent yields with excellent regioselectivity. The Royal Society of Chemistry 2019-09-30 /pmc/articles/PMC9072218/ /pubmed/35529353 http://dx.doi.org/10.1039/c9ra07694h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Lu, Jiaqing Man, Yuning Zhang, Yabin Lin, Bo Lin, Qi Weng, Zhiqiang Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
title | Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
title_full | Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
title_fullStr | Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
title_full_unstemmed | Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
title_short | Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
title_sort | copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072218/ https://www.ncbi.nlm.nih.gov/pubmed/35529353 http://dx.doi.org/10.1039/c9ra07694h |
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