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Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis
Au(iii)-aryl species have been unequivocally identified as reactive intermediates in oxidant-free C–O and C–N cross coupling catalysis. The crystal structures of cyclometalated neutral and cationic Au(iii) species are described and their key role in 2 electron-redox Au(i)/Au(iii) catalysis in C–O an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452266/ https://www.ncbi.nlm.nih.gov/pubmed/28572904 http://dx.doi.org/10.1039/c6sc03699f |
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author | Serra, Jordi Parella, Teodor Ribas, Xavi |
author_facet | Serra, Jordi Parella, Teodor Ribas, Xavi |
author_sort | Serra, Jordi |
collection | PubMed |
description | Au(iii)-aryl species have been unequivocally identified as reactive intermediates in oxidant-free C–O and C–N cross coupling catalysis. The crystal structures of cyclometalated neutral and cationic Au(iii) species are described and their key role in 2 electron-redox Au(i)/Au(iii) catalysis in C–O and C–N cross couplings is shown. Nucleophiles compatible with Au-catalyzed cross couplings include aromatic and aliphatic alcohols and amines, as well as water and amides. |
format | Online Article Text |
id | pubmed-5452266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-54522662017-06-01 Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis Serra, Jordi Parella, Teodor Ribas, Xavi Chem Sci Chemistry Au(iii)-aryl species have been unequivocally identified as reactive intermediates in oxidant-free C–O and C–N cross coupling catalysis. The crystal structures of cyclometalated neutral and cationic Au(iii) species are described and their key role in 2 electron-redox Au(i)/Au(iii) catalysis in C–O and C–N cross couplings is shown. Nucleophiles compatible with Au-catalyzed cross couplings include aromatic and aliphatic alcohols and amines, as well as water and amides. Royal Society of Chemistry 2017-02-01 2016-09-23 /pmc/articles/PMC5452266/ /pubmed/28572904 http://dx.doi.org/10.1039/c6sc03699f Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Serra, Jordi Parella, Teodor Ribas, Xavi Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis |
title | Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis
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title_full | Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis
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title_fullStr | Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis
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title_full_unstemmed | Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis
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title_short | Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis
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title_sort | au(iii)-aryl intermediates in oxidant-free c–n and c–o cross-coupling catalysis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452266/ https://www.ncbi.nlm.nih.gov/pubmed/28572904 http://dx.doi.org/10.1039/c6sc03699f |
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