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volume 16 issue 9 pages 789-794

Sodium acetate catalyzed tandem Knoevenagel–Michael multicomponent reaction of aldehydes, 2-pyrazolin-5-ones, and cyano-functionalized C–H acids: Facile and efficient way to 3-(5-hydroxypyrazol-4-yl)-3-aryl-propionitriles

Publication typeJournal Article
Publication date2013-04-16
scimago Q3
wos Q4
SJR0.209
CiteScore2.3
Impact factor0.6
ISSN16310748, 18781543
General Chemistry
General Chemical Engineering
Abstract
Sodium acetate catalyzed multicomponent reaction of aryl aldehydes, 2-pyrazolin-5-ones, and malononitrile or alkyl cyanoacetates in alcohols results in the formation of substituted 3-(5-hydroxy-3-methylpyrazol-4-yl)-3-arylpropionitriles in 80–99% yields. The developed efficient catalytic approach to the substituted 3-(5-hydroxy-3-methylpyrazol-4-yl)-3-arylpropionitriles – the promising compounds for human cardiovascular diseases therapy and different biomedical applications – is beneficial from the viewpoint of diversity-oriented large-scale processes and represents facile, efficient and environmentally benign synthetic concept for multicomponent reactions strategy.
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Elinson M. N. et al. Sodium acetate catalyzed tandem Knoevenagel–Michael multicomponent reaction of aldehydes, 2-pyrazolin-5-ones, and cyano-functionalized C–H acids: Facile and efficient way to 3-(5-hydroxypyrazol-4-yl)-3-aryl-propionitriles // Comptes Rendus Chimie. 2013. Vol. 16. No. 9. pp. 789-794.
GOST all authors (up to 50) Copy
Elinson M. N., Elinson M. N., Nasybullin R. F., Nikishin G. I. Sodium acetate catalyzed tandem Knoevenagel–Michael multicomponent reaction of aldehydes, 2-pyrazolin-5-ones, and cyano-functionalized C–H acids: Facile and efficient way to 3-(5-hydroxypyrazol-4-yl)-3-aryl-propionitriles // Comptes Rendus Chimie. 2013. Vol. 16. No. 9. pp. 789-794.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1016/j.crci.2013.03.003
UR - https://comptes-rendus.academie-sciences.fr/chimie/articles/10.1016/j.crci.2013.03.003/
TI - Sodium acetate catalyzed tandem Knoevenagel–Michael multicomponent reaction of aldehydes, 2-pyrazolin-5-ones, and cyano-functionalized C–H acids: Facile and efficient way to 3-(5-hydroxypyrazol-4-yl)-3-aryl-propionitriles
T2 - Comptes Rendus Chimie
AU - Elinson, M. N.
AU - Elinson, Michail N
AU - Nasybullin, Ruslan F
AU - Nikishin, Gennady I.
PY - 2013
DA - 2013/04/16
PB - Cellule MathDoc/Centre Mersenne
SP - 789-794
IS - 9
VL - 16
SN - 1631-0748
SN - 1878-1543
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2013_Elinson,
author = {M. N. Elinson and Michail N Elinson and Ruslan F Nasybullin and Gennady I. Nikishin},
title = {Sodium acetate catalyzed tandem Knoevenagel–Michael multicomponent reaction of aldehydes, 2-pyrazolin-5-ones, and cyano-functionalized C–H acids: Facile and efficient way to 3-(5-hydroxypyrazol-4-yl)-3-aryl-propionitriles},
journal = {Comptes Rendus Chimie},
year = {2013},
volume = {16},
publisher = {Cellule MathDoc/Centre Mersenne},
month = {apr},
url = {https://comptes-rendus.academie-sciences.fr/chimie/articles/10.1016/j.crci.2013.03.003/},
number = {9},
pages = {789--794},
doi = {10.1016/j.crci.2013.03.003}
}
MLA
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MLA Copy
Elinson, M. N., et al. “Sodium acetate catalyzed tandem Knoevenagel–Michael multicomponent reaction of aldehydes, 2-pyrazolin-5-ones, and cyano-functionalized C–H acids: Facile and efficient way to 3-(5-hydroxypyrazol-4-yl)-3-aryl-propionitriles.” Comptes Rendus Chimie, vol. 16, no. 9, Apr. 2013, pp. 789-794. https://comptes-rendus.academie-sciences.fr/chimie/articles/10.1016/j.crci.2013.03.003/.