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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...

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Detalles Bibliográficos
Autores principales: Li, Yahui, Bao, Gao, Wu, Xiao-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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