Aza-Michael Reactions in Ionic Liquids. A Facile Synthesis of β-Amino Compounds

2003 ◽  
Vol 32 (11) ◽  
pp. 988-989 ◽  
Author(s):  
J. S. Yadav ◽  
B. V. S. Reddy ◽  
A. K. Basak ◽  
A. V. Narsaiah
Keyword(s):  
Ionic Liquids ◽  
Facile Synthesis ◽  
Michael Reactions ◽  
Amino Compounds

Aza-Michael Reactions in Ionic Liquids. A Facile Synthesis of β-Amino Compounds.

ChemInform ◽  
2004 ◽  
Vol 35 (14) ◽  
Author(s):  
J. S. Yadav ◽  
B. V. S. Reddy ◽  
A. K. Basak ◽  
A. V. Narsaiah
Keyword(s):  
Ionic Liquids ◽  
Facile Synthesis ◽  
Michael Reactions ◽  
Amino Compounds

Facile Synthesis of Novel Ionic Liquids Containing Dithiocarbamate

2005 ◽  
Vol 35 (4) ◽  
pp. 521-526 ◽  
Author(s):  
Dingjun Zhang ◽  
Jianmin Chen ◽  
Yongming Liang ◽  
Huidi Zhou
Keyword(s):  
Ionic Liquids ◽  
Facile Synthesis

First Example of Ionic Liquids Promoted Domino Knoevenagel Hetero-Diels—Alder Reactions: A Facile Synthesis of Pyrano[3,2-c]coumarins.

ChemInform ◽  
2005 ◽  
Vol 36 (1) ◽  
Author(s):  
J. S. Yadav ◽  
B. V. S. Reddy ◽  
V. Naveenkumar ◽  
R. Srinivasa Rao ◽  
K. Nagaiah
Keyword(s):  
Ionic Liquids ◽  
Diels Alder ◽  
Facile Synthesis

Facile Synthesis of Copper Nanoparticles by Ionic Liquids and Its Application to Facilitated Olefin Transport Membranes

2009 ◽  
Vol 48 (15) ◽  
pp. 7437-7441 ◽  
Author(s):  
Jongho Kim ◽  
Sang Wook Kang ◽  
Sung Hyun Mun ◽  
Yong Soo Kang
Keyword(s):  
Ionic Liquids ◽  
Copper Nanoparticles ◽  
Facile Synthesis

scholarly journals Beneficial Contribution of Biosourced Ionic Liquids and Microwaves in the Michael Reaction

Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 814
Author(s):  
Katia Bacha ◽  
Kawther Aguibi ◽  
Jean-Pierre Mbakidi ◽  
Sandrine Bouquillon
Keyword(s):  
Ionic Liquids ◽  
Reaction Time ◽  
Michael Reaction ◽  
Chiral Ionic Liquids ◽  
Michael Reactions ◽  
Basic Catalysts ◽  
The Michael Reaction

We developed a synthesis of chiral ionic liquids from proline and one of its derivatives. Nine chiral ionic liquids were synthesized with yields from 78% to 95%. These synthesized ionic liquids played two roles in Michael reactions, as solvents, and as basic catalysts, where the ionic phase could also be reused at least five times without loss of activity. The yields up to 99% were improved by increasing the amount of dimethylmalonate from 1.2 equivalents to 3 or 4 equivalents. Furthermore, the reaction time could be reduced from 24 h to 45 min through microwaves activation.

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