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Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF

[Image: see text] The nickel-catalyzed amination of aryl O-sulfamates and chlorides using the green solvent 2-methyl-THF is reported. This methodology employs the commercially available and air-stable precatalyst NiCl(2)(DME), is broad in scope, and provides access to aryl amines in synthetically us...

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Autores principales: Fine Nathel, Noah F., Kim, Junyong, Hie, Liana, Jiang, Xingyu, Garg, Neil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165539/
https://www.ncbi.nlm.nih.gov/pubmed/25243095
http://dx.doi.org/10.1021/cs501045v
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author Fine Nathel, Noah F.
Kim, Junyong
Hie, Liana
Jiang, Xingyu
Garg, Neil K.
author_facet Fine Nathel, Noah F.
Kim, Junyong
Hie, Liana
Jiang, Xingyu
Garg, Neil K.
author_sort Fine Nathel, Noah F.
collection PubMed
description [Image: see text] The nickel-catalyzed amination of aryl O-sulfamates and chlorides using the green solvent 2-methyl-THF is reported. This methodology employs the commercially available and air-stable precatalyst NiCl(2)(DME), is broad in scope, and provides access to aryl amines in synthetically useful yields. The utility of this methodology is underscored by examples of gram-scale couplings conducted with catalyst loadings as low as 1 mol % nickel. Moreover, the nickel-catalyzed amination described is tolerant of heterocycles and should prove useful in the synthesis of pharmaceutical candidates and other heteroatom-containing compounds.
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spelling pubmed-41655392015-08-20 Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF Fine Nathel, Noah F. Kim, Junyong Hie, Liana Jiang, Xingyu Garg, Neil K. ACS Catal [Image: see text] The nickel-catalyzed amination of aryl O-sulfamates and chlorides using the green solvent 2-methyl-THF is reported. This methodology employs the commercially available and air-stable precatalyst NiCl(2)(DME), is broad in scope, and provides access to aryl amines in synthetically useful yields. The utility of this methodology is underscored by examples of gram-scale couplings conducted with catalyst loadings as low as 1 mol % nickel. Moreover, the nickel-catalyzed amination described is tolerant of heterocycles and should prove useful in the synthesis of pharmaceutical candidates and other heteroatom-containing compounds. American Chemical Society 2014-08-20 2014-09-05 /pmc/articles/PMC4165539/ /pubmed/25243095 http://dx.doi.org/10.1021/cs501045v Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Fine Nathel, Noah F.
Kim, Junyong
Hie, Liana
Jiang, Xingyu
Garg, Neil K.
Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
title Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
title_full Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
title_fullStr Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
title_full_unstemmed Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
title_short Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF
title_sort nickel-catalyzed amination of aryl chlorides and sulfamates in 2-methyl-thf
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165539/
https://www.ncbi.nlm.nih.gov/pubmed/25243095
http://dx.doi.org/10.1021/cs501045v
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