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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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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. |
format | Online Article Text |
id | pubmed-4165539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
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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