Cargando…
General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis
[Image: see text] Using a simple copper catalyst, the alkylation of nitroalkanes with α-bromocarbonyls is now possible. This method provides a general, functional group tolerant route to β-nitrocarbonyl compounds, including nitro amides, esters, ketones, and aldehydes. The highly sterically dense, f...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051431/ https://www.ncbi.nlm.nih.gov/pubmed/24870052 http://dx.doi.org/10.1021/ol5014153 |
_version_ | 1782320096284246016 |
---|---|
author | Gietter, Amber A. S. Gildner, Peter G. Cinderella, Andrew P. Watson, Donald A. |
author_facet | Gietter, Amber A. S. Gildner, Peter G. Cinderella, Andrew P. Watson, Donald A. |
author_sort | Gietter, Amber A. S. |
collection | PubMed |
description | [Image: see text] Using a simple copper catalyst, the alkylation of nitroalkanes with α-bromocarbonyls is now possible. This method provides a general, functional group tolerant route to β-nitrocarbonyl compounds, including nitro amides, esters, ketones, and aldehydes. The highly sterically dense, functional group rich products from these reactions can be readily elaborated into a range of complex nitrogen-containing molecules, including highly substituted β-amino acids. |
format | Online Article Text |
id | pubmed-4051431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40514312015-05-28 General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis Gietter, Amber A. S. Gildner, Peter G. Cinderella, Andrew P. Watson, Donald A. Org Lett [Image: see text] Using a simple copper catalyst, the alkylation of nitroalkanes with α-bromocarbonyls is now possible. This method provides a general, functional group tolerant route to β-nitrocarbonyl compounds, including nitro amides, esters, ketones, and aldehydes. The highly sterically dense, functional group rich products from these reactions can be readily elaborated into a range of complex nitrogen-containing molecules, including highly substituted β-amino acids. American Chemical Society 2014-05-28 2014-06-06 /pmc/articles/PMC4051431/ /pubmed/24870052 http://dx.doi.org/10.1021/ol5014153 Text en Copyright © 2014 American Chemical Society |
spellingShingle | Gietter, Amber A. S. Gildner, Peter G. Cinderella, Andrew P. Watson, Donald A. General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis |
title | General Route for Preparing β-Nitrocarbonyl
Compounds Using Copper Thermal Redox Catalysis |
title_full | General Route for Preparing β-Nitrocarbonyl
Compounds Using Copper Thermal Redox Catalysis |
title_fullStr | General Route for Preparing β-Nitrocarbonyl
Compounds Using Copper Thermal Redox Catalysis |
title_full_unstemmed | General Route for Preparing β-Nitrocarbonyl
Compounds Using Copper Thermal Redox Catalysis |
title_short | General Route for Preparing β-Nitrocarbonyl
Compounds Using Copper Thermal Redox Catalysis |
title_sort | general route for preparing β-nitrocarbonyl
compounds using copper thermal redox catalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051431/ https://www.ncbi.nlm.nih.gov/pubmed/24870052 http://dx.doi.org/10.1021/ol5014153 |
work_keys_str_mv | AT gietteramberas generalrouteforpreparingbnitrocarbonylcompoundsusingcopperthermalredoxcatalysis AT gildnerpeterg generalrouteforpreparingbnitrocarbonylcompoundsusingcopperthermalredoxcatalysis AT cinderellaandrewp generalrouteforpreparingbnitrocarbonylcompoundsusingcopperthermalredoxcatalysis AT watsondonalda generalrouteforpreparingbnitrocarbonylcompoundsusingcopperthermalredoxcatalysis |