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Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester
A selective copper (Cu)-catalyzed C–S bond direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester was developed. Notably, various biologically active 5-phenyl-3-phenylsulfanylpenta-2,4-dienoic acid ethyl ester derivatives were efficiently synthesized under moderate conditions....
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/PMC9083087/ https://www.ncbi.nlm.nih.gov/pubmed/35541071 http://dx.doi.org/10.1039/c8ra05311a |
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author | Cai, Rongrong Zhou, Zhuoda Chai, Qianqian Zhu, Yueer Xu, Runsheng |
author_facet | Cai, Rongrong Zhou, Zhuoda Chai, Qianqian Zhu, Yueer Xu, Runsheng |
author_sort | Cai, Rongrong |
collection | PubMed |
description | A selective copper (Cu)-catalyzed C–S bond direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester was developed. Notably, various biologically active 5-phenyl-3-phenylsulfanylpenta-2,4-dienoic acid ethyl ester derivatives were efficiently synthesized under moderate conditions. Finally, a plausible Cu(i)/Cu(iii) reaction mechanism was proposed. |
format | Online Article Text |
id | pubmed-9083087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90830872022-05-09 Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester Cai, Rongrong Zhou, Zhuoda Chai, Qianqian Zhu, Yueer Xu, Runsheng RSC Adv Chemistry A selective copper (Cu)-catalyzed C–S bond direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester was developed. Notably, various biologically active 5-phenyl-3-phenylsulfanylpenta-2,4-dienoic acid ethyl ester derivatives were efficiently synthesized under moderate conditions. Finally, a plausible Cu(i)/Cu(iii) reaction mechanism was proposed. The Royal Society of Chemistry 2018-07-27 /pmc/articles/PMC9083087/ /pubmed/35541071 http://dx.doi.org/10.1039/c8ra05311a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Cai, Rongrong Zhou, Zhuoda Chai, Qianqian Zhu, Yueer Xu, Runsheng Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
title | Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
title_full | Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
title_fullStr | Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
title_full_unstemmed | Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
title_short | Copper-catalyzed C–S direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
title_sort | copper-catalyzed c–s direct cross-coupling of thiols with 5-arylpenta-2,4-dienoic acid ethyl ester |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083087/ https://www.ncbi.nlm.nih.gov/pubmed/35541071 http://dx.doi.org/10.1039/c8ra05311a |
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