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Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes

[Image: see text] The selective FeCl(3)-catalyzed oxidative cross-coupling reaction between phenols and primary, secondary, and tertiary 2-aminonaphthalene derivatives was investigated. The generality of this scalable method provides a sustainable alternative for preparing N,O-biaryl compounds that...

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Autores principales: Vershinin, Vlada, Forkosh, Hagit, Ben-Lulu, Mor, Libman, Anna, Pappo, Doron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783733/
https://www.ncbi.nlm.nih.gov/pubmed/33296193
http://dx.doi.org/10.1021/acs.joc.0c00874
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author Vershinin, Vlada
Forkosh, Hagit
Ben-Lulu, Mor
Libman, Anna
Pappo, Doron
author_facet Vershinin, Vlada
Forkosh, Hagit
Ben-Lulu, Mor
Libman, Anna
Pappo, Doron
author_sort Vershinin, Vlada
collection PubMed
description [Image: see text] The selective FeCl(3)-catalyzed oxidative cross-coupling reaction between phenols and primary, secondary, and tertiary 2-aminonaphthalene derivatives was investigated. The generality of this scalable method provides a sustainable alternative for preparing N,O-biaryl compounds that are widely used as ligands and catalysts. Based on a comprehensive kinetic investigation, a catalytic cycle involving a ternary complex that binds to both the coupling partners and the oxidant during the key oxidative coupling step is postulated. Furthermore, the studies showed that the reaction is regulated by off-cycle acid–base and ligand exchange processes.
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spelling pubmed-77837332021-01-06 Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes Vershinin, Vlada Forkosh, Hagit Ben-Lulu, Mor Libman, Anna Pappo, Doron J Org Chem [Image: see text] The selective FeCl(3)-catalyzed oxidative cross-coupling reaction between phenols and primary, secondary, and tertiary 2-aminonaphthalene derivatives was investigated. The generality of this scalable method provides a sustainable alternative for preparing N,O-biaryl compounds that are widely used as ligands and catalysts. Based on a comprehensive kinetic investigation, a catalytic cycle involving a ternary complex that binds to both the coupling partners and the oxidant during the key oxidative coupling step is postulated. Furthermore, the studies showed that the reaction is regulated by off-cycle acid–base and ligand exchange processes. American Chemical Society 2020-12-09 2021-01-01 /pmc/articles/PMC7783733/ /pubmed/33296193 http://dx.doi.org/10.1021/acs.joc.0c00874 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Vershinin, Vlada
Forkosh, Hagit
Ben-Lulu, Mor
Libman, Anna
Pappo, Doron
Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
title Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
title_full Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
title_fullStr Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
title_full_unstemmed Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
title_short Mechanistic Insights into the FeCl(3)-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
title_sort mechanistic insights into the fecl(3)-catalyzed oxidative cross-coupling of phenols with 2-aminonaphthalenes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783733/
https://www.ncbi.nlm.nih.gov/pubmed/33296193
http://dx.doi.org/10.1021/acs.joc.0c00874
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