ChemInform Abstract: Synthesis of Functionalized 2-Aminohydropyridines and 2-Pyridinones via Domino Reactions of Arylamines, Methyl Propiolate, Aromatic Aldehydes, and Substituted Acetonitriles.

ChemInform ◽  
2011 ◽  
Vol 42 (48) ◽  
pp. no-no
Author(s):  
Jing Sun ◽  
Yan Sun ◽  
Er-Yan Xia ◽  
Chao-Guo Yan
Tetrahedron ◽  
2010 ◽  
Vol 66 (11) ◽  
pp. 1990-1993 ◽  
Author(s):  
Xi Chen ◽  
Wei Chen ◽  
Li Wang ◽  
Xiao-Qi Yu ◽  
De-Shun Huang ◽  
...  

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.


Author(s):  
Veerappan Jeyachandranan

A library of novel benzo[b] thiophenehave been synthesized regioselectively in good yields through the one-pot domino reactions of thiophenone, malononitrile and aromatic aldehydes in the presence of NaOEt. This transformation presumably involves Knoevenagel condensation–Michael addition–intramolecular Thorpe-Ziegler cyclization-Tautomerization-Elimination sequence of reactions.


ChemInform ◽  
2010 ◽  
Vol 41 (27) ◽  
pp. no-no
Author(s):  
Xi Chen ◽  
Wei Chen ◽  
Li Wang ◽  
Xiao-Qi Yu ◽  
De-Shun Huang ◽  
...  

2020 ◽  
Author(s):  
Kirsten Anne Hewitt ◽  
Erika L. Lucas ◽  
Elizabeth R. Jarvo ◽  
Anthony Castro
Keyword(s):  

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