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Palladium-catalysed synthesis of triaryl(heteroaryl)methanes
Tetraarylmethane derivatives are desirable for a variety of applications, but difficult to access with modern C–C bond-forming reactions. Here we report a straightforward method for palladium-catalysed arylation of aryl(heteroaryl)methanes and diaryl(heteroaryl)methanes with aryl chlorides. This rea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355892/ https://www.ncbi.nlm.nih.gov/pubmed/28290445 http://dx.doi.org/10.1038/ncomms14641 |
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author | Zhang, Shuguang Kim, Byeong-Seon Wu, Chen Mao, Jianyou Walsh, Patrick J. |
author_facet | Zhang, Shuguang Kim, Byeong-Seon Wu, Chen Mao, Jianyou Walsh, Patrick J. |
author_sort | Zhang, Shuguang |
collection | PubMed |
description | Tetraarylmethane derivatives are desirable for a variety of applications, but difficult to access with modern C–C bond-forming reactions. Here we report a straightforward method for palladium-catalysed arylation of aryl(heteroaryl)methanes and diaryl(heteroaryl)methanes with aryl chlorides. This reaction enables introduction of various aryl groups to construct triaryl(heteroaryl)methanes via a C–H functionalization in good to excellent yield, and represents the first step towards a general transition metal catalysed synthesis of tetraarylmethanes. |
format | Online Article Text |
id | pubmed-5355892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53558922017-04-17 Palladium-catalysed synthesis of triaryl(heteroaryl)methanes Zhang, Shuguang Kim, Byeong-Seon Wu, Chen Mao, Jianyou Walsh, Patrick J. Nat Commun Article Tetraarylmethane derivatives are desirable for a variety of applications, but difficult to access with modern C–C bond-forming reactions. Here we report a straightforward method for palladium-catalysed arylation of aryl(heteroaryl)methanes and diaryl(heteroaryl)methanes with aryl chlorides. This reaction enables introduction of various aryl groups to construct triaryl(heteroaryl)methanes via a C–H functionalization in good to excellent yield, and represents the first step towards a general transition metal catalysed synthesis of tetraarylmethanes. Nature Publishing Group 2017-03-14 /pmc/articles/PMC5355892/ /pubmed/28290445 http://dx.doi.org/10.1038/ncomms14641 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhang, Shuguang Kim, Byeong-Seon Wu, Chen Mao, Jianyou Walsh, Patrick J. Palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
title | Palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
title_full | Palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
title_fullStr | Palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
title_full_unstemmed | Palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
title_short | Palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
title_sort | palladium-catalysed synthesis of triaryl(heteroaryl)methanes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355892/ https://www.ncbi.nlm.nih.gov/pubmed/28290445 http://dx.doi.org/10.1038/ncomms14641 |
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