Functionalized Periodic Mesoporous Organosilica: A Highly Enantioselective Catalyst for the Michael Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes

2012 ◽  
Vol 18 (48) ◽  
pp. 15546-15553 ◽  
Author(s):  
Ketang Liu ◽  
Ronghua Jin ◽  
Tanyu Cheng ◽  
Xiangming Xu ◽  
Fei Gao ◽  
...  
Keyword(s):  
Michael Addition ◽  
Periodic Mesoporous Organosilica ◽  
Dicarbonyl Compounds ◽  
Mesoporous Organosilica ◽  
Enantioselective Catalyst ◽  
The Michael Addition

Synthesis of C3-nitroalkylated-4-hydroxycoumarin and hydroxyiminodihydrofuroquinolinone derivatives via the Michael addition of cyclic 1,3-dicarbonyl compounds to β-nitrostyrenes

Tetrahedron ◽  
2011 ◽  
Vol 67 (16) ◽  
pp. 2870-2877 ◽  
Author(s):  
Deepak Kumar Barange ◽  
Veerababurao Kavala ◽  
Chun-Wei Kuo ◽  
Po-Min Lei ◽  
Ching-Fa Yao
Keyword(s):  
Michael Addition ◽  
Dicarbonyl Compounds ◽  
The Michael Addition

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

2012 ◽  
Vol 8 ◽  
pp. 534-538 ◽  
Author(s):  
Zong-Bo Xie ◽  
Na Wang ◽  
Ming-Yu Wu ◽  
Ting He ◽  
Zhang-Gao Le ◽  
...  
Keyword(s):  
Michael Addition ◽  
Solvent Free ◽  
Environmentally Benign ◽  
Dicarbonyl Compounds ◽  
Catalyst Free ◽  
Grinding Method ◽  
Solvent Free Conditions ◽  
The Michael Addition

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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