Electroorganic synthesis. 4. Facile synthesis of aromatic aldehydes by direct anodic oxidation of p-substituted toluenes

1985 ◽  
Vol 50 (4) ◽  
pp. 539-541 ◽  
Author(s):  
Ikuzo Nishiguchi ◽  
Tsuneaki Hirashima
2000 ◽  
Vol 2 (15) ◽  
pp. 2295-2298 ◽  
Author(s):  
Kanak Kanti Majumdar ◽  
Chien-Hong Cheng

2012 ◽  
Vol 8 ◽  
pp. 1839-1843 ◽  
Author(s):  
Jing Sun ◽  
Hong Gao ◽  
Qun Wu ◽  
Chao-Guo Yan

In the presence of p-toluenesulfonic acid as catalyst the domino reaction of arylamines, methyl propiolates and aromatic aldehydes in ethanol proceeded smoothly to give polysubstituted 1,2,3,4-tetrahydroquinolines in moderate yields. The reaction is believed to involve the Povarov reaction of in situ generated β-enamino ester with the in situ formed aromatic imine.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
S. Sudha ◽  
M. A. Pasha

Synthesis of an assembly of structurally importantN-H- andN-substituted acridine-1,8-diones by CAN (ceric ammonium nitrate) catalysed one-pot four-component reaction of electron-deficient and electron-rich aromatic aldehydes and aromatic amines or ammonium acetate and dimedone or cyclohexyl-1,3-diones at 26°C under sonic condition is reported. The method is clean and energy efficient as it uses a greener method and an eco-friendly catalyst.


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