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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...

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Autores principales: Gietter, Amber A. S., Gildner, Peter G., Cinderella, Andrew P., Watson, Donald A.
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
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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.
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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
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