PART I: NOVEL QUINOXALINE DERIVATIVES OF BIOLOGICAL INTEREST

2001 ◽  
Vol 24 (2) ◽  
pp. 135-144
Author(s):  
M. Badran ◽  
S. Botros ◽  
A. El-Gendy ◽  
N. Abdou ◽  
H. El-Assi ◽  
...  
1993 ◽  
Vol 58 (8) ◽  
pp. 1963-1968 ◽  
Author(s):  
Abdel-Alim M. Abdel-Alim ◽  
Abdel-Nasser A. El-Shorbagi ◽  
Mahmoud A. El-Gendy ◽  
Hosny A. H. El-Shareif

2-Methyl-4(3H)-quinazolines carrying alkyl, cycloalkyl, aralkyl or aryl substituents at N-3 of the quinazoline ring exhibit analgetic, antipyretic and antiinflammatory activities comparable to those of aspirin and phenylbutazone. In our previous work, various 4(3H)-quinazoline derivatives were prepared. The present communication is a continuation of our effort in this field.


1982 ◽  
Vol 13 (13) ◽  
Author(s):  
G. BASTIAN ◽  
L. RENE ◽  
J.-P. BUISSON ◽  
R. ROYER ◽  
D. AVERBECK ◽  
...  

2011 ◽  
Vol 76 (9) ◽  
pp. 1191-1198 ◽  
Author(s):  
Bahador Karami ◽  
Saeed Khodabakhshi

Convenient and simple procedures for the synthesis of phenazine and quinoxaline derivatives were developed via a reaction of ophenylenediamines and 1,2-dicarbonyl compounds. In addition, the synthesis of two new derivatives of 1,4-benzo diazine derivatives and the catalytic activity of magnesium sulfate heptahydrate (MgSO4?7H2O) in the room temperature condensation of o-phenylenediamines and 1,2- dicarbonyl compounds in ethanol as solvent are reported. This method has many appealing attributes, such as excellent yields, short reactions times, and simple work-up procedures.


2012 ◽  
Vol 22 (7) ◽  
pp. 3341-3349 ◽  
Author(s):  
Bhimagouda S. Patil ◽  
G. Krishnamurthy ◽  
M. R. Lokesh ◽  
N. D. Shashikumar ◽  
H. S. Bhojya Naik ◽  
...  

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