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Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions

Phenols are extremely valuable building blocks in the areas of pharmaceuticals, natural products, materials and catalysts. In order to carry out modifications on phenols, the phenolic oxygen is routinely protected to prevent unwanted side reactions. Presently many of the protecting groups available...

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Detalles Bibliográficos
Autores principales: Brittain, William D. G., Cobb, Steven L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390695/
https://www.ncbi.nlm.nih.gov/pubmed/30623945
http://dx.doi.org/10.1039/c8ob02899k
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author Brittain, William D. G.
Cobb, Steven L.
author_facet Brittain, William D. G.
Cobb, Steven L.
author_sort Brittain, William D. G.
collection PubMed
description Phenols are extremely valuable building blocks in the areas of pharmaceuticals, natural products, materials and catalysts. In order to carry out modifications on phenols, the phenolic oxygen is routinely protected to prevent unwanted side reactions. Presently many of the protecting groups available can require harsh conditions, specialist equipment, expensive or air/moisture-sensitive reagents to install and remove. Here we introduce the use of the tetrafluoropyridyl (TFP) group as a general protecting group for phenols. TFP can be installed in one step with no sensitivity to water or air, and it is stable under a range of commonly employed reaction conditions including acid and base. The TFP protecting group is readily cleaved under mild conditions with quantitative conversion to the parent phenol, observed in many cases in less than 1 hour.
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spelling pubmed-63906952019-03-15 Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions Brittain, William D. G. Cobb, Steven L. Org Biomol Chem Chemistry Phenols are extremely valuable building blocks in the areas of pharmaceuticals, natural products, materials and catalysts. In order to carry out modifications on phenols, the phenolic oxygen is routinely protected to prevent unwanted side reactions. Presently many of the protecting groups available can require harsh conditions, specialist equipment, expensive or air/moisture-sensitive reagents to install and remove. Here we introduce the use of the tetrafluoropyridyl (TFP) group as a general protecting group for phenols. TFP can be installed in one step with no sensitivity to water or air, and it is stable under a range of commonly employed reaction conditions including acid and base. The TFP protecting group is readily cleaved under mild conditions with quantitative conversion to the parent phenol, observed in many cases in less than 1 hour. Royal Society of Chemistry 2019-02-28 2019-01-09 /pmc/articles/PMC6390695/ /pubmed/30623945 http://dx.doi.org/10.1039/c8ob02899k Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Brittain, William D. G.
Cobb, Steven L.
Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions
title Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions
title_full Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions
title_fullStr Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions
title_full_unstemmed Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions
title_short Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions
title_sort tetrafluoropyridyl (tfp): a general phenol protecting group readily cleaved under mild conditions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390695/
https://www.ncbi.nlm.nih.gov/pubmed/30623945
http://dx.doi.org/10.1039/c8ob02899k
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