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Khalafy, Jabbar,Rimaz, Mehdi,Panahi, Leila,Rabiei, Hossein Korean Chemical Society 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
A series of new 4-aryl-6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones have been synthesized via three component reaction of 1,3-dimethylbarbituric acid with arylglyoxals in the presence of hydrazinium dihydrochloride in ethanol. All of these derivatives may act as potential monoamine oxidase inhibitors.
Khalafy, Jabbar,Rimaz, Mehdi,Ezzati, Mahnaz,Prager, Rolf H. Korean Chemical Society 2012 Bulletin of the Korean Chemical Society Vol.33 No.9
A simple regioselective synthesis of cinnoline derivatives was achieved by a one-pot three component synthetic methodology. New substituted 7,8-dihydrocinnolin-5(6H)-ones are prepared via one-pot three component reaction of arylglyoxals with 1,3-cyclohexanedione and dimedone in the presence of hydrazine hydrate in moderate to good yields.
Jabbar Khalafy,Mehdi Rimaz,Leila Panahi,Hossein Rabiei 대한화학회 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
A series of new 4-aryl-6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones have been synthesized via three component reaction of 1,3-dimethylbarbituric acid with arylglyoxals in the presence of hydrazinium dihydrochloride in ethanol. All of these derivatives may act as potential monoamine oxidase inhibitors.
Jabbar Khalafy,Mehdi Rimaz,Mahnaz Ezzati,Rolf. H. Prager 대한화학회 2012 Bulletin of the Korean Chemical Society Vol.33 No.9
A simple regioselective synthesis of cinnoline derivatives was achieved by a one-pot three component synthetic methodology. New substituted 7,8-dihydrocinnolin-5(6H)-ones are prepared via one-pot three component reaction of arylglyoxals with 1,3-cyclohexanedione and dimedone in the presence of hydrazine hydrate in moderate to good yields.
Synthesis of Some Pyrimido[4,5-b]quinoline Derivatives
Marjani, Ahmad Poursattar,Khalafy, Jabbar,Ebrahimlo, Ali Reza Molla,Prager, Rolf.H. Korean Chemical Society 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
A series of pyrimidoquinoline derivatives was synthesized in good yield and short reaction times by reaction of 3-arylaminoisoxazol-5(2H)-ones with derivatives of 2-chloro-3-formylquinoline in toluene under reflux conditions.
Synthesis of Some Pyrimido[4,5-b]quinoline Derivatives
Ahmad Poursattar Marjani,Ali Reza Molla Ebrahimlo,Rolf. H. Prager,Jabbar Khalafy 대한화학회 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
A series of pyrimidoquinoline derivatives was synthesized in good yield and short reaction times by reaction of 3-arylaminoisoxazol-5(2H)-ones with derivatives of 2-chloro-3-formylquinoline in toluene under reflux conditions.