Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method

An environmentally benign, fast and convenient protocol has been developed for the Michael addition of 1,3-dicarbonyl compounds to β-nitroalkenes in good to excellent yields by a grinding method under catalyst- and solvent-free conditions.

Detalles Bibliográficos
Autores principales: Xie, Zong-Bo, Wang, Na, Wu, Ming-Yu, He, Ting, Le, Zhang-Gao, Yu, Xiao-Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343280/
https://www.ncbi.nlm.nih.gov/pubmed/22563352
http://dx.doi.org/10.3762/bjoc.8.61
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author Xie, Zong-Bo
Wang, Na
Wu, Ming-Yu
He, Ting
Le, Zhang-Gao
Yu, Xiao-Qi
author_facet Xie, Zong-Bo
Wang, Na
Wu, Ming-Yu
He, Ting
Le, Zhang-Gao
Yu, Xiao-Qi
author_sort Xie, Zong-Bo
collection PubMed
description An environmentally benign, fast and convenient protocol has been developed for the Michael addition of 1,3-dicarbonyl compounds to β-nitroalkenes in good to excellent yields by a grinding method under catalyst- and solvent-free conditions.
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spelling pubmed-33432802012-05-04 Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method Xie, Zong-Bo Wang, Na Wu, Ming-Yu He, Ting Le, Zhang-Gao Yu, Xiao-Qi Beilstein J Org Chem Full Research Paper An environmentally benign, fast and convenient protocol has been developed for the Michael addition of 1,3-dicarbonyl compounds to β-nitroalkenes in good to excellent yields by a grinding method under catalyst- and solvent-free conditions. Beilstein-Institut 2012-04-11 /pmc/articles/PMC3343280/ /pubmed/22563352 http://dx.doi.org/10.3762/bjoc.8.61 Text en Copyright © 2012, Xie et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Xie, Zong-Bo
Wang, Na
Wu, Ming-Yu
He, Ting
Le, Zhang-Gao
Yu, Xiao-Qi
Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
title Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
title_full Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
title_fullStr Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
title_full_unstemmed Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
title_short Catalyst-free and solvent-free Michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
title_sort catalyst-free and solvent-free michael addition of 1,3-dicarbonyl compounds to nitroalkenes by a grinding method
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343280/
https://www.ncbi.nlm.nih.gov/pubmed/22563352
http://dx.doi.org/10.3762/bjoc.8.61
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