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Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic Acids with Pyrazolones
[Image: see text] A copper-mediated decarboxylative coupling reaction of 3-indoleacetic acids with pyrazolones was described. This protocol realized new functionalization of pyrazolones under simple reaction conditions and exhibited high functional group compatibility and broad substrate scope. Nota...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851627/ https://www.ncbi.nlm.nih.gov/pubmed/35187342 http://dx.doi.org/10.1021/acsomega.1c06443 |
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author | Wen, Kangmei Wu, Yinrong Chen, Jiewen Shi, Jie Zheng, Mulin Yao, Xingang Tang, Xiaodong |
author_facet | Wen, Kangmei Wu, Yinrong Chen, Jiewen Shi, Jie Zheng, Mulin Yao, Xingang Tang, Xiaodong |
author_sort | Wen, Kangmei |
collection | PubMed |
description | [Image: see text] A copper-mediated decarboxylative coupling reaction of 3-indoleacetic acids with pyrazolones was described. This protocol realized new functionalization of pyrazolones under simple reaction conditions and exhibited high functional group compatibility and broad substrate scope. Notably, the products displayed antiproliferative activity against cancer cells. |
format | Online Article Text |
id | pubmed-8851627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88516272022-02-18 Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic Acids with Pyrazolones Wen, Kangmei Wu, Yinrong Chen, Jiewen Shi, Jie Zheng, Mulin Yao, Xingang Tang, Xiaodong ACS Omega [Image: see text] A copper-mediated decarboxylative coupling reaction of 3-indoleacetic acids with pyrazolones was described. This protocol realized new functionalization of pyrazolones under simple reaction conditions and exhibited high functional group compatibility and broad substrate scope. Notably, the products displayed antiproliferative activity against cancer cells. American Chemical Society 2022-02-02 /pmc/articles/PMC8851627/ /pubmed/35187342 http://dx.doi.org/10.1021/acsomega.1c06443 Text en © 2022 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 | Wen, Kangmei Wu, Yinrong Chen, Jiewen Shi, Jie Zheng, Mulin Yao, Xingang Tang, Xiaodong Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic Acids with Pyrazolones |
title | Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic
Acids with Pyrazolones |
title_full | Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic
Acids with Pyrazolones |
title_fullStr | Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic
Acids with Pyrazolones |
title_full_unstemmed | Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic
Acids with Pyrazolones |
title_short | Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic
Acids with Pyrazolones |
title_sort | copper-mediated decarboxylative coupling of 3-indoleacetic
acids with pyrazolones |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851627/ https://www.ncbi.nlm.nih.gov/pubmed/35187342 http://dx.doi.org/10.1021/acsomega.1c06443 |
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