ChemInform Abstract: Highly Efficient Michael Addition Reaction of Amines Catalyzed by Silica-Supported Aluminum Chloride.

ChemInform ◽  
2009 ◽  
Vol 40 (33) ◽  
Author(s):  
Mohammad R. Saidi ◽  
Yaghoub Pourshojaei ◽  
Fezzeh Aryanasab
2008 ◽  
Vol 39 (1) ◽  
pp. 139-157 ◽  
Author(s):  
Abdolkarim Zare ◽  
Alireza Hasaninejad ◽  
Mohammad Hassan Beyzavi ◽  
Ahmad Reza Moosavi Zare ◽  
Ali Khalafi-Nezhad ◽  
...  

2015 ◽  
Vol 13 (7) ◽  
pp. 1992-1995 ◽  
Author(s):  
Jiazhu Li ◽  
Yang Liu ◽  
Xi-Sen Xu ◽  
Yan-Long Li ◽  
Shan-Guo Zhang ◽  
...  

pH-Dependent regioselective condensation of methyl mesopyropheophorbide a with HCHO is studied and stereoselective Michael reaction of the 132-methylene product is also discussed.


2020 ◽  
Vol 49 (35) ◽  
pp. 12365-12371
Author(s):  
Xiu-Fang Mo ◽  
Chang-Feng Xiong ◽  
Ze-Wen Chen ◽  
Chao Liu ◽  
Piao He ◽  
...  

Zinc complexes supported by pyridine-N-oxide ligands show highly efficient catalysis for Michael addition reaction. The NMR and MS experiments analysis displays intermediate [Zn(SR)2(HSR)4] has real catalytic activity for the addition reactions.


2015 ◽  
Vol 2 (8) ◽  
pp. 956-960 ◽  
Author(s):  
Dian-Feng Chen ◽  
Chen-long Zhang ◽  
Yue Hu ◽  
Zhi-Yong Han ◽  
Liu-Zhu Gong

Rh(ii)/chiral phosphine combined catalysis has been developed for a highly efficient sequential C–H functionalization/asymmetric allylation or Michael addition reaction to afford a diverse range of quaternary 3,3′-indolyloxindole derivatives.


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