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Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings
A mild and fully catalytic aryl–aryl cross coupling via gold-catalysed C–H activation has been achieved by merging gold and photoredox catalysis. The procedure is free of stoichiometric oxidants and additives, which were previously required in gold-catalysed C–H activation reactions. Exploiting dual...
Autores principales: | , , |
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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/PMC5427993/ https://www.ncbi.nlm.nih.gov/pubmed/28553527 http://dx.doi.org/10.1039/c6sc05469b |
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author | Gauchot, V. Sutherland, D. R. Lee, A.-L. |
author_facet | Gauchot, V. Sutherland, D. R. Lee, A.-L. |
author_sort | Gauchot, V. |
collection | PubMed |
description | A mild and fully catalytic aryl–aryl cross coupling via gold-catalysed C–H activation has been achieved by merging gold and photoredox catalysis. The procedure is free of stoichiometric oxidants and additives, which were previously required in gold-catalysed C–H activation reactions. Exploiting dual gold and photoredox catalysis confers regioselectivity via the crucial gold-catalysed C–H activation step, which is not present in the unselective photocatalysis-only counterpart. |
format | Online Article Text |
id | pubmed-5427993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-54279932017-05-26 Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings Gauchot, V. Sutherland, D. R. Lee, A.-L. Chem Sci Chemistry A mild and fully catalytic aryl–aryl cross coupling via gold-catalysed C–H activation has been achieved by merging gold and photoredox catalysis. The procedure is free of stoichiometric oxidants and additives, which were previously required in gold-catalysed C–H activation reactions. Exploiting dual gold and photoredox catalysis confers regioselectivity via the crucial gold-catalysed C–H activation step, which is not present in the unselective photocatalysis-only counterpart. Royal Society of Chemistry 2017-04-01 2017-01-27 /pmc/articles/PMC5427993/ /pubmed/28553527 http://dx.doi.org/10.1039/c6sc05469b Text en This journal is © The Royal Society of Chemistry 2017 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 Gauchot, V. Sutherland, D. R. Lee, A.-L. Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings |
title | Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings
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title_full | Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings
|
title_fullStr | Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings
|
title_full_unstemmed | Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings
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title_short | Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings
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title_sort | dual gold and photoredox catalysed c–h activation of arenes for aryl–aryl cross couplings |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427993/ https://www.ncbi.nlm.nih.gov/pubmed/28553527 http://dx.doi.org/10.1039/c6sc05469b |
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