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Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds

The first heterogeneous catalyzed example for the direct synthesis of aromatic ketones via intermolecular carbopalladation of aliphatic nitriles and organoboron compounds was developed. This mild method proceeds with a supported palladium nanoparticles catalyst that could be reused and recycled five...

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Autores principales: Liu, Xin, Liu, Dan, Muschin, Tegshi, Bao, Agula, Bai, Chaolumen, Bao, Yong-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124771/
https://www.ncbi.nlm.nih.gov/pubmed/35615308
http://dx.doi.org/10.3389/fchem.2022.855850
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author Liu, Xin
Liu, Dan
Muschin, Tegshi
Bao, Agula
Bai, Chaolumen
Bao, Yong-Sheng
author_facet Liu, Xin
Liu, Dan
Muschin, Tegshi
Bao, Agula
Bai, Chaolumen
Bao, Yong-Sheng
author_sort Liu, Xin
collection PubMed
description The first heterogeneous catalyzed example for the direct synthesis of aromatic ketones via intermolecular carbopalladation of aliphatic nitriles and organoboron compounds was developed. This mild method proceeds with a supported palladium nanoparticles catalyst that could be reused and recycled five times. The fresh and used catalysts were characterized by XPS and TEM. The XPS analysis indicated that Pd(0) was the active species for the reaction. This methodology provides a mild and cost-effective strategy for the efficient synthesis of ketones.
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spelling pubmed-91247712022-05-24 Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds Liu, Xin Liu, Dan Muschin, Tegshi Bao, Agula Bai, Chaolumen Bao, Yong-Sheng Front Chem Chemistry The first heterogeneous catalyzed example for the direct synthesis of aromatic ketones via intermolecular carbopalladation of aliphatic nitriles and organoboron compounds was developed. This mild method proceeds with a supported palladium nanoparticles catalyst that could be reused and recycled five times. The fresh and used catalysts were characterized by XPS and TEM. The XPS analysis indicated that Pd(0) was the active species for the reaction. This methodology provides a mild and cost-effective strategy for the efficient synthesis of ketones. Frontiers Media S.A. 2022-05-09 /pmc/articles/PMC9124771/ /pubmed/35615308 http://dx.doi.org/10.3389/fchem.2022.855850 Text en Copyright © 2022 Liu, Liu, Muschin, Bao, Bai and Bao. 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
Liu, Xin
Liu, Dan
Muschin, Tegshi
Bao, Agula
Bai, Chaolumen
Bao, Yong-Sheng
Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds
title Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds
title_full Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds
title_fullStr Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds
title_full_unstemmed Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds
title_short Supported Palladium Nanoparticles Catalyzed Intermolecular Carbopalladation of Nitriles and Organoboron Compounds
title_sort supported palladium nanoparticles catalyzed intermolecular carbopalladation of nitriles and organoboron compounds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124771/
https://www.ncbi.nlm.nih.gov/pubmed/35615308
http://dx.doi.org/10.3389/fchem.2022.855850
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