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Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups
Synthetic methods for the preparation of thioketals featuring CF(3) groups are rare. Here, we have developed a copper-catalyzed thioketalization of enones bearing CF(3) groups and various mercaptans. 24 thioketal molecules have been obtained with moderate to excellent yield. Meanwhile, a preparative...
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/PMC9033665/ https://www.ncbi.nlm.nih.gov/pubmed/35479255 http://dx.doi.org/10.1039/d1ra03222d |
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author | Zhang, Tongfei Gao, Zhenbo |
author_facet | Zhang, Tongfei Gao, Zhenbo |
author_sort | Zhang, Tongfei |
collection | PubMed |
description | Synthetic methods for the preparation of thioketals featuring CF(3) groups are rare. Here, we have developed a copper-catalyzed thioketalization of enones bearing CF(3) groups and various mercaptans. 24 thioketal molecules have been obtained with moderate to excellent yield. Meanwhile, a preparative scale experiment has been performed giving over 95% yield. This work allows the straightforward formation of thioketals containing CF(3) groups and unsaturated double bonds. |
format | Online Article Text |
id | pubmed-9033665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90336652022-04-26 Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups Zhang, Tongfei Gao, Zhenbo RSC Adv Chemistry Synthetic methods for the preparation of thioketals featuring CF(3) groups are rare. Here, we have developed a copper-catalyzed thioketalization of enones bearing CF(3) groups and various mercaptans. 24 thioketal molecules have been obtained with moderate to excellent yield. Meanwhile, a preparative scale experiment has been performed giving over 95% yield. This work allows the straightforward formation of thioketals containing CF(3) groups and unsaturated double bonds. The Royal Society of Chemistry 2021-06-01 /pmc/articles/PMC9033665/ /pubmed/35479255 http://dx.doi.org/10.1039/d1ra03222d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhang, Tongfei Gao, Zhenbo Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
title | Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
title_full | Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
title_fullStr | Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
title_full_unstemmed | Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
title_short | Copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
title_sort | copper-catalyzed thioketalization of enones featuring trifluoromethyl groups |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033665/ https://www.ncbi.nlm.nih.gov/pubmed/35479255 http://dx.doi.org/10.1039/d1ra03222d |
work_keys_str_mv | AT zhangtongfei coppercatalyzedthioketalizationofenonesfeaturingtrifluoromethylgroups AT gaozhenbo coppercatalyzedthioketalizationofenonesfeaturingtrifluoromethylgroups |