Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant

The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mi...

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Autores principales: Sdahl, Mark, Conrad, Jürgen, Braunberger, Christina, Beifuss, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065379/
https://www.ncbi.nlm.nih.gov/pubmed/35519358
http://dx.doi.org/10.1039/c9ra02541c
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author Sdahl, Mark
Conrad, Jürgen
Braunberger, Christina
Beifuss, Uwe
author_facet Sdahl, Mark
Conrad, Jürgen
Braunberger, Christina
Beifuss, Uwe
author_sort Sdahl, Mark
collection PubMed
description The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions.
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spelling pubmed-90653792022-05-04 Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant Sdahl, Mark Conrad, Jürgen Braunberger, Christina Beifuss, Uwe RSC Adv Chemistry The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions. The Royal Society of Chemistry 2019-06-21 /pmc/articles/PMC9065379/ /pubmed/35519358 http://dx.doi.org/10.1039/c9ra02541c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Sdahl, Mark
Conrad, Jürgen
Braunberger, Christina
Beifuss, Uwe
Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant
title Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant
title_full Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant
title_fullStr Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant
title_full_unstemmed Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant
title_short Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O(2) as oxidant
title_sort efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using ki as iodine source and aerial o(2) as oxidant
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065379/
https://www.ncbi.nlm.nih.gov/pubmed/35519358
http://dx.doi.org/10.1039/c9ra02541c
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AT braunbergerchristina efficientandsustainablelaccasecatalyzediodinationofpsubstitutedphenolsusingkiasiodinesourceandaerialo2asoxidant
AT beifussuwe efficientandsustainablelaccasecatalyzediodinationofpsubstitutedphenolsusingkiasiodinesourceandaerialo2asoxidant

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