An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8

A mild and efficient method for the ipso-hydroxylation of arylboronic acids to the corresponding phenols was developed using (NH4)2S2O8 as an oxidizing agent. The reactions were performed under metal-, ligand-, and base-free conditions.

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Main Authors: Claudia A. Contreras-Celedón, Luis Chacón-García, Nancy Judith Lira-Corral
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2014/569572
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author Claudia A. Contreras-Celedón
Luis Chacón-García
Nancy Judith Lira-Corral
author_facet Claudia A. Contreras-Celedón
Luis Chacón-García
Nancy Judith Lira-Corral
author_sort Claudia A. Contreras-Celedón
collection DOAJ
description A mild and efficient method for the ipso-hydroxylation of arylboronic acids to the corresponding phenols was developed using (NH4)2S2O8 as an oxidizing agent. The reactions were performed under metal-, ligand-, and base-free conditions.
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institution Kabale University
issn 2090-9063
2090-9071
language English
publishDate 2014-01-01
publisher Wiley
record_format Article
series Journal of Chemistry
spelling doaj-art-0ccc9b741b7348619c99cf60bc6a5cce2025-08-20T03:54:15ZengWileyJournal of Chemistry2090-90632090-90712014-01-01201410.1155/2014/569572569572An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8Claudia A. Contreras-Celedón0Luis Chacón-García1Nancy Judith Lira-Corral2Laboratorio de Diseño Molecular, Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Edificio B-1, Ciudad Universitaria, 58030 Morelia, MICH, MexicoLaboratorio de Diseño Molecular, Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Edificio B-1, Ciudad Universitaria, 58030 Morelia, MICH, MexicoLaboratorio de Diseño Molecular, Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Edificio B-1, Ciudad Universitaria, 58030 Morelia, MICH, MexicoA mild and efficient method for the ipso-hydroxylation of arylboronic acids to the corresponding phenols was developed using (NH4)2S2O8 as an oxidizing agent. The reactions were performed under metal-, ligand-, and base-free conditions.http://dx.doi.org/10.1155/2014/569572
spellingShingle Claudia A. Contreras-Celedón
Luis Chacón-García
Nancy Judith Lira-Corral
An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8
Journal of Chemistry
title An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8
title_full An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8
title_fullStr An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8
title_full_unstemmed An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8
title_short An Efficient Synthesis of Phenols via Oxidative Hydroxylation of Arylboronic Acids Using (NH4)2S2O8
title_sort efficient synthesis of phenols via oxidative hydroxylation of arylboronic acids using nh4 2s2o8
url http://dx.doi.org/10.1155/2014/569572
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