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An unprecedented palladium-arsenic catalytic cycle for nitriles hydration

An unprecedented palladium/arsenic-based catalytic cycle for the hydration of nitriles to the corresponding amides is here described. It occurs in exceptionally mild conditions such as neutral pH and moderate temperature (60°C). The versatility of this new catalytic cycle was tested on various nitri...

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Autores principales: Cirri, Damiano, Marzo, Tiziano, Pratesi, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440694/
https://www.ncbi.nlm.nih.gov/pubmed/37608865
http://dx.doi.org/10.3389/fchem.2023.1253008
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author Cirri, Damiano
Marzo, Tiziano
Pratesi, Alessandro
author_facet Cirri, Damiano
Marzo, Tiziano
Pratesi, Alessandro
author_sort Cirri, Damiano
collection PubMed
description An unprecedented palladium/arsenic-based catalytic cycle for the hydration of nitriles to the corresponding amides is here described. It occurs in exceptionally mild conditions such as neutral pH and moderate temperature (60°C). The versatility of this new catalytic cycle was tested on various nitriles from aliphatic to aromatic. Also, the effect of ring substitution with electron withdrawing and electron donating groups was investigated in the cases of aromatic nitriles, as well as the effect of potentially interferent functional groups such as hydroxy group or pyridinic nitrogen. Furthermore, a pilot study on the potential suitability of this approach for its scale-up is presented, revealing that the catalytic cycle could be potentially and quickly scaled up.
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spelling pubmed-104406942023-08-22 An unprecedented palladium-arsenic catalytic cycle for nitriles hydration Cirri, Damiano Marzo, Tiziano Pratesi, Alessandro Front Chem Chemistry An unprecedented palladium/arsenic-based catalytic cycle for the hydration of nitriles to the corresponding amides is here described. It occurs in exceptionally mild conditions such as neutral pH and moderate temperature (60°C). The versatility of this new catalytic cycle was tested on various nitriles from aliphatic to aromatic. Also, the effect of ring substitution with electron withdrawing and electron donating groups was investigated in the cases of aromatic nitriles, as well as the effect of potentially interferent functional groups such as hydroxy group or pyridinic nitrogen. Furthermore, a pilot study on the potential suitability of this approach for its scale-up is presented, revealing that the catalytic cycle could be potentially and quickly scaled up. Frontiers Media S.A. 2023-08-07 /pmc/articles/PMC10440694/ /pubmed/37608865 http://dx.doi.org/10.3389/fchem.2023.1253008 Text en Copyright © 2023 Cirri, Marzo and Pratesi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Cirri, Damiano
Marzo, Tiziano
Pratesi, Alessandro
An unprecedented palladium-arsenic catalytic cycle for nitriles hydration
title An unprecedented palladium-arsenic catalytic cycle for nitriles hydration
title_full An unprecedented palladium-arsenic catalytic cycle for nitriles hydration
title_fullStr An unprecedented palladium-arsenic catalytic cycle for nitriles hydration
title_full_unstemmed An unprecedented palladium-arsenic catalytic cycle for nitriles hydration
title_short An unprecedented palladium-arsenic catalytic cycle for nitriles hydration
title_sort unprecedented palladium-arsenic catalytic cycle for nitriles hydration
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440694/
https://www.ncbi.nlm.nih.gov/pubmed/37608865
http://dx.doi.org/10.3389/fchem.2023.1253008
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