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Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters
Functional group transfer reactions are an important synthetic tool in modern organic synthesis. Herein, we developed a new palladium-catalyzed intermolecular transthioetherification reaction of aryl halides with thioethers and thioesters. The synthetic utility and practicality of this catalytic pro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150098/ https://www.ncbi.nlm.nih.gov/pubmed/34123310 http://dx.doi.org/10.1039/c9sc05532k |
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author | Li, Yahui Bao, Gao Wu, Xiao-Feng |
author_facet | Li, Yahui Bao, Gao Wu, Xiao-Feng |
author_sort | Li, Yahui |
collection | PubMed |
description | Functional group transfer reactions are an important synthetic tool in modern organic synthesis. Herein, we developed a new palladium-catalyzed intermolecular transthioetherification reaction of aryl halides with thioethers and thioesters. The synthetic utility and practicality of this catalytic protocol are demonstrated in a wide range of successful transformations (>70 examples). This catalytic protocol is applicable in carbonylative coupling processes as well, and the first example of carbonylative methylthioesterification of aryl halides has been achieved. Notably, this work also provides an approach to using natural products, such as methionine and selenomethionine, as the functional group sources. |
format | Online Article Text |
id | pubmed-8150098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81500982021-06-11 Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters Li, Yahui Bao, Gao Wu, Xiao-Feng Chem Sci Chemistry Functional group transfer reactions are an important synthetic tool in modern organic synthesis. Herein, we developed a new palladium-catalyzed intermolecular transthioetherification reaction of aryl halides with thioethers and thioesters. The synthetic utility and practicality of this catalytic protocol are demonstrated in a wide range of successful transformations (>70 examples). This catalytic protocol is applicable in carbonylative coupling processes as well, and the first example of carbonylative methylthioesterification of aryl halides has been achieved. Notably, this work also provides an approach to using natural products, such as methionine and selenomethionine, as the functional group sources. The Royal Society of Chemistry 2020-01-22 /pmc/articles/PMC8150098/ /pubmed/34123310 http://dx.doi.org/10.1039/c9sc05532k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Li, Yahui Bao, Gao Wu, Xiao-Feng Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
title | Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
title_full | Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
title_fullStr | Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
title_full_unstemmed | Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
title_short | Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
title_sort | palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150098/ https://www.ncbi.nlm.nih.gov/pubmed/34123310 http://dx.doi.org/10.1039/c9sc05532k |
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