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High chemoselectivity in the phenol synthesis
Efforts to trap early intermediates of the gold-catalyzed phenol synthesis failed. Neither inter- nor intramolecularly offered vinyl groups, ketones or alcohols were able to intercept the gold carbenoid species. This indicates that the competing steps of the gold-catalyzed phenol synthesis are much...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135103/ https://www.ncbi.nlm.nih.gov/pubmed/21804874 http://dx.doi.org/10.3762/bjoc.7.90 |
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author | Rudolph, Matthias McCreery, Melissa Q Frey, Wolfgang Hashmi, A Stephen K |
author_facet | Rudolph, Matthias McCreery, Melissa Q Frey, Wolfgang Hashmi, A Stephen K |
author_sort | Rudolph, Matthias |
collection | PubMed |
description | Efforts to trap early intermediates of the gold-catalyzed phenol synthesis failed. Neither inter- nor intramolecularly offered vinyl groups, ketones or alcohols were able to intercept the gold carbenoid species. This indicates that the competing steps of the gold-catalyzed phenol synthesis are much faster than the steps of the interception reaction. In the latter the barrier of activation is higher. At the same time this explains the high tolerance of this very efficient and general reaction towards functional groups. |
format | Online Article Text |
id | pubmed-3135103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-31351032011-07-29 High chemoselectivity in the phenol synthesis Rudolph, Matthias McCreery, Melissa Q Frey, Wolfgang Hashmi, A Stephen K Beilstein J Org Chem Full Research Paper Efforts to trap early intermediates of the gold-catalyzed phenol synthesis failed. Neither inter- nor intramolecularly offered vinyl groups, ketones or alcohols were able to intercept the gold carbenoid species. This indicates that the competing steps of the gold-catalyzed phenol synthesis are much faster than the steps of the interception reaction. In the latter the barrier of activation is higher. At the same time this explains the high tolerance of this very efficient and general reaction towards functional groups. Beilstein-Institut 2011-06-10 /pmc/articles/PMC3135103/ /pubmed/21804874 http://dx.doi.org/10.3762/bjoc.7.90 Text en Copyright © 2011, Rudolph et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), 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 | Full Research Paper Rudolph, Matthias McCreery, Melissa Q Frey, Wolfgang Hashmi, A Stephen K High chemoselectivity in the phenol synthesis |
title | High chemoselectivity in the phenol synthesis |
title_full | High chemoselectivity in the phenol synthesis |
title_fullStr | High chemoselectivity in the phenol synthesis |
title_full_unstemmed | High chemoselectivity in the phenol synthesis |
title_short | High chemoselectivity in the phenol synthesis |
title_sort | high chemoselectivity in the phenol synthesis |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135103/ https://www.ncbi.nlm.nih.gov/pubmed/21804874 http://dx.doi.org/10.3762/bjoc.7.90 |
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