An Approach to Polysubstituted Triazipines, Thiadiazoles and Thiazoles Based on Benzopyran Moiety Through The Utility of Versatile Hydrazonoyl Halides asIn VitroMonoamine Oxidase Inhibitors

2016 ◽  
Vol 54 (2) ◽  
pp. 1215-1227 ◽  
Author(s):  
Mohamed G. Badrey ◽  
Sobhi M. Gomha ◽  
Wael A. A. Arafa ◽  
Mohamed M. Abdulla
Keyword(s):  
2007 ◽  
Vol 182 (10) ◽  
pp. 2409-2418 ◽  
Author(s):  
Abdou O. Abdelhamid ◽  
Zeineb H. Ismail ◽  
Marwa S. El Gendy ◽  
Moustafa M. Ghorab

2008 ◽  
Vol 63 (5) ◽  
pp. 585-590 ◽  
Author(s):  
Hany M. Dalloul ◽  
El-Hossain A. R. Mohamed ◽  
Ali Z. El-Shorafa

A series of new 3,5,6-thiadiaza-4-hexenoates (4a - k) were synthesized from the reaction of the corresponding hydrazonoyl halides 1 with ethyl mercaptoacetate (3). These compounds underwent intramolecular cyclization to 1,3,4-thiadiazin-5-one derivatives (5a - k) in the presence of MeONa or LiH. The structures of the synthesized compounds were confirmed by their elemental analyses and spectral data.


2013 ◽  
Vol 78 (8) ◽  
pp. 1119-1125 ◽  
Author(s):  
Sobhi Gomha ◽  
Hatem Abdel-Aziz

New functionalized 1,2,4-triazolo-[4,3-b]-1,2,4-triazino-[5,6-b]indole derivatives were synthesized via reaction of the hydrazonoyl halides with 5H-2,3-dihydro-1,2,4-triazino[5,6-b]indole-3-thione or its 3-methylthio derivative. The mechanism and the regioselectivity of the studied reactions have been discussed.


Synthesis ◽  
2006 ◽  
Vol 2006 (01) ◽  
pp. 59-62 ◽  
Author(s):  
Saad Makhseed ◽  
Balkis AL-Saleh ◽  
Huwaida M. Hassaneen ◽  
Mohamed Hilmy Elnagdi

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