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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...

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Autores principales: Rudolph, Matthias, McCreery, Melissa Q, Frey, Wolfgang, Hashmi, A Stephen K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
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.
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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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