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Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis

With the increasing concern for sustainability, the use of environmentally friendly media to perform chemical processes has attracted the attention of many research groups. Among them, the use of water, as the unique solvent for reactions, is currently an active area of research. One process of part...

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Autores principales: Ortiz, Rosa, Herrera, Raquel P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154297/
https://www.ncbi.nlm.nih.gov/pubmed/28368309
http://dx.doi.org/10.3390/molecules22040574
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author Ortiz, Rosa
Herrera, Raquel P.
author_facet Ortiz, Rosa
Herrera, Raquel P.
author_sort Ortiz, Rosa
collection PubMed
description With the increasing concern for sustainability, the use of environmentally friendly media to perform chemical processes has attracted the attention of many research groups. Among them, the use of water, as the unique solvent for reactions, is currently an active area of research. One process of particular interest is the direct nucleophilic substitution of an alcohol avoiding its preliminary transformation into a good leaving group, since one of the by-products in this approach would be water. The direct substitution of allylic, benzylic, and tertiary alcohols has been achieved through S(N)1-type reactions with catalytic amounts of Brønsted or Lewis acids; however, organic solvents are often required. In this review, the pioneering S(N)1 approaches performed in pure water and in the absence of a metal based Lewis acid are compiled and discussed.
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spelling pubmed-61542972018-11-13 Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis Ortiz, Rosa Herrera, Raquel P. Molecules Review With the increasing concern for sustainability, the use of environmentally friendly media to perform chemical processes has attracted the attention of many research groups. Among them, the use of water, as the unique solvent for reactions, is currently an active area of research. One process of particular interest is the direct nucleophilic substitution of an alcohol avoiding its preliminary transformation into a good leaving group, since one of the by-products in this approach would be water. The direct substitution of allylic, benzylic, and tertiary alcohols has been achieved through S(N)1-type reactions with catalytic amounts of Brønsted or Lewis acids; however, organic solvents are often required. In this review, the pioneering S(N)1 approaches performed in pure water and in the absence of a metal based Lewis acid are compiled and discussed. MDPI 2017-04-01 /pmc/articles/PMC6154297/ /pubmed/28368309 http://dx.doi.org/10.3390/molecules22040574 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ortiz, Rosa
Herrera, Raquel P.
Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis
title Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis
title_full Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis
title_fullStr Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis
title_full_unstemmed Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis
title_short Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis
title_sort direct substitution of alcohols in pure water by brønsted acid catalysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154297/
https://www.ncbi.nlm.nih.gov/pubmed/28368309
http://dx.doi.org/10.3390/molecules22040574
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