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An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature

A highly efficient nickel/silver co-catalyzed C–H amination at the C5 position of 8-aminoquinolines with azodicarboxylates at room temperature is reported. The reaction undergoes a self-redox process without the necessity of external oxidant. It proceeded under simple and mild conditions without any...

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Detalles Bibliográficos
Autores principales: Zhao, Ruinan, Yang, Yaocheng, Wang, Xia, Ren, Peng, Zhang, Qian, Li, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088955/
https://www.ncbi.nlm.nih.gov/pubmed/35557799
http://dx.doi.org/10.1039/c8ra07647b
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author Zhao, Ruinan
Yang, Yaocheng
Wang, Xia
Ren, Peng
Zhang, Qian
Li, Dong
author_facet Zhao, Ruinan
Yang, Yaocheng
Wang, Xia
Ren, Peng
Zhang, Qian
Li, Dong
author_sort Zhao, Ruinan
collection PubMed
description A highly efficient nickel/silver co-catalyzed C–H amination at the C5 position of 8-aminoquinolines with azodicarboxylates at room temperature is reported. The reaction undergoes a self-redox process without the necessity of external oxidant. It proceeded under simple and mild conditions without any additional ligand, base or oxidant and provided the desired products in good to excellent yields. This method also possessed the merits of good functional group compatibility and air and moisture tolerance. It provides an efficient strategy for the synthesis of useful quinoline derivatives.
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spelling pubmed-90889552022-05-11 An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature Zhao, Ruinan Yang, Yaocheng Wang, Xia Ren, Peng Zhang, Qian Li, Dong RSC Adv Chemistry A highly efficient nickel/silver co-catalyzed C–H amination at the C5 position of 8-aminoquinolines with azodicarboxylates at room temperature is reported. The reaction undergoes a self-redox process without the necessity of external oxidant. It proceeded under simple and mild conditions without any additional ligand, base or oxidant and provided the desired products in good to excellent yields. This method also possessed the merits of good functional group compatibility and air and moisture tolerance. It provides an efficient strategy for the synthesis of useful quinoline derivatives. The Royal Society of Chemistry 2018-11-05 /pmc/articles/PMC9088955/ /pubmed/35557799 http://dx.doi.org/10.1039/c8ra07647b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhao, Ruinan
Yang, Yaocheng
Wang, Xia
Ren, Peng
Zhang, Qian
Li, Dong
An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature
title An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature
title_full An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature
title_fullStr An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature
title_full_unstemmed An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature
title_short An efficient nickel/silver co-catalyzed remote C–H amination of 8-aminoquinolines with azodicarboxylates at room temperature
title_sort efficient nickel/silver co-catalyzed remote c–h amination of 8-aminoquinolines with azodicarboxylates at room temperature
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088955/
https://www.ncbi.nlm.nih.gov/pubmed/35557799
http://dx.doi.org/10.1039/c8ra07647b
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