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Transition-metal-catalyzed synthesis of phenols and aryl thiols
Phenols and aryl thiols are fundamental building blocks in organic synthesis and final products with interesting biological activities. Over the past decades, substantial progress has been made in transition-metal-catalyzed coupling reactions, which resulted in the emergence of new methods for the s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372758/ https://www.ncbi.nlm.nih.gov/pubmed/28405239 http://dx.doi.org/10.3762/bjoc.13.58 |
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author | Liu, Yajun Liu, Shasha Xiao, Yan |
author_facet | Liu, Yajun Liu, Shasha Xiao, Yan |
author_sort | Liu, Yajun |
collection | PubMed |
description | Phenols and aryl thiols are fundamental building blocks in organic synthesis and final products with interesting biological activities. Over the past decades, substantial progress has been made in transition-metal-catalyzed coupling reactions, which resulted in the emergence of new methods for the synthesis of phenols and aryl thiols. Aryl halides have been extensively studied as substrates for the synthesis of phenols and aryl thiols. In very recent years, C–H activation represents a powerful strategy for the construction of functionalized phenols directly from various arenes. However, the synthesis of aryl thiols through C–H activation has not been reported. In this review, a brief overview is given of the recent advances in synthetic strategies for both phenols and aryl thiols. |
format | Online Article Text |
id | pubmed-5372758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-53727582017-04-12 Transition-metal-catalyzed synthesis of phenols and aryl thiols Liu, Yajun Liu, Shasha Xiao, Yan Beilstein J Org Chem Review Phenols and aryl thiols are fundamental building blocks in organic synthesis and final products with interesting biological activities. Over the past decades, substantial progress has been made in transition-metal-catalyzed coupling reactions, which resulted in the emergence of new methods for the synthesis of phenols and aryl thiols. Aryl halides have been extensively studied as substrates for the synthesis of phenols and aryl thiols. In very recent years, C–H activation represents a powerful strategy for the construction of functionalized phenols directly from various arenes. However, the synthesis of aryl thiols through C–H activation has not been reported. In this review, a brief overview is given of the recent advances in synthetic strategies for both phenols and aryl thiols. Beilstein-Institut 2017-03-23 /pmc/articles/PMC5372758/ /pubmed/28405239 http://dx.doi.org/10.3762/bjoc.13.58 Text en Copyright © 2017, Liu et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Liu, Yajun Liu, Shasha Xiao, Yan Transition-metal-catalyzed synthesis of phenols and aryl thiols |
title | Transition-metal-catalyzed synthesis of phenols and aryl thiols |
title_full | Transition-metal-catalyzed synthesis of phenols and aryl thiols |
title_fullStr | Transition-metal-catalyzed synthesis of phenols and aryl thiols |
title_full_unstemmed | Transition-metal-catalyzed synthesis of phenols and aryl thiols |
title_short | Transition-metal-catalyzed synthesis of phenols and aryl thiols |
title_sort | transition-metal-catalyzed synthesis of phenols and aryl thiols |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372758/ https://www.ncbi.nlm.nih.gov/pubmed/28405239 http://dx.doi.org/10.3762/bjoc.13.58 |
work_keys_str_mv | AT liuyajun transitionmetalcatalyzedsynthesisofphenolsandarylthiols AT liushasha transitionmetalcatalyzedsynthesisofphenolsandarylthiols AT xiaoyan transitionmetalcatalyzedsynthesisofphenolsandarylthiols |