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Articles 1 - 7 of 7
Full-Text Articles in Physical Sciences and Mathematics
One Step Synthesis Of Some 2,5,6-Trisubstituted-1,3-Dioxin-4-Ones, Ahmet Şener, İshak Bi̇ldi̇ri̇ci̇, Hasan Genç, Nuretti̇n Mengeş, Siddik Eski̇noba
One Step Synthesis Of Some 2,5,6-Trisubstituted-1,3-Dioxin-4-Ones, Ahmet Şener, İshak Bi̇ldi̇ri̇ci̇, Hasan Genç, Nuretti̇n Mengeş, Siddik Eski̇noba
Turkish Journal of Chemistry
A number of novel 2,5,6-trisubstituted-1,3-dioxin-4-one derivatives were synthesized via one step reactions between dibenzoylmethane or benzoylacetone and oxalyl chloride in refluxing solvents containing various aldehydes.
Synthesis And Characterization Of Novel Azole Heterocycles Based On 2,5-Disubstituted Thiadiazole, Nadia A. Salih
Synthesis And Characterization Of Novel Azole Heterocycles Based On 2,5-Disubstituted Thiadiazole, Nadia A. Salih
Turkish Journal of Chemistry
Starting from 2-amino-5-mercapto-1,3,4-thiadiazole (1), a variety of new 1,2,4-triazino[5,4-b][1,3,4] thiadiazole (3), pyrazole (4), [1,2,4]triazolo[3,4-b] [1,3,4]thiadiazole (5), phthalazine-3,6-dione (6), azo derivatives (9), pyrimidine -2,4,6-trione (11), Schiff base (12) and pyrrolidine (13) derivatives have been synthesized. All proposed structures were supported by FT-IR, ^1H-NMR, ^{13}C-NMR elemental analysis, and MS spectroscopic data.
Synthesis And Characterizations Of Some New 4h-1,2,4-Triazole Derivatives, Nesli̇han Demi̇rbaş, Ahmet Demi̇rbaş, Şule Ceylan, Deni̇z Şahi̇n
Synthesis And Characterizations Of Some New 4h-1,2,4-Triazole Derivatives, Nesli̇han Demi̇rbaş, Ahmet Demi̇rbaş, Şule Ceylan, Deni̇z Şahi̇n
Turkish Journal of Chemistry
3-[(5-Amino-1,3,4-thiadiazol-2-yl)methyl]-4-ethoxycarbonylamino-5-alkyl-4H-1,2,4-triazoles (2a,b) were obtained from the reaction of 3-cyanomethyl-5-alkyl-4-ethoxycarbonylamino-4H-1,2,4-triazoles (1a,b) with thiosemicarbazide in the presence of trifluoroacetic acid. The treatment of the obtained compounds (2a,b) with acetic anhydride for 1 h afforded 3-[(5-acetylamino-1,3,4-thiadiazol-2-yl)methyl]-4-ethoxycarbonylamino-5-alkyl-4H-1,2,4-triazoles (3a,b). The synthesis of 4-ethoxycarbonylamino-3-[(2,3-dihydro-1,3-benzoxazol-2-yl)methyl]-5-(4-methylbenzyl)-4H-1,2,4-triazole (4) was performed by the treatment of 3-[(5-acetylamino-1,3,4-thiadiazol-2-yl)methyl]-4-ethoxycarbonylamino-5-(4-methylbenzyl)-4H-1,2,4-triazole (3a) with o-aminophenol under nitrogen atmosphere for 50 h. The reaction of compounds 1a,b with salicylaldehyde in the presence of sodium ethoxide yielded 2-{4-[(ethoxycarbonyl)amino]-5-alkyl-4H-1,2,4-triazol-3-yl}-3-(2-hydroxyphenyl)-acrylonitriles (5a,b). The acetylations of compounds 5a,b with acetic anhydride for 5 h resulted in the formation of 2-{4-[acetyl(ethoxycarbonyl)amino]-5-alkyl-4H-1,2,4-triazol-3-yl}-3-[2-(acetyloxy)phenyl]-acrylic acids (6a,b). On the other hand, the treatment of compounds 5a,b with …
Preparation Of 1,5-Diketones By Addition Of Cyclohexanone To Chalcones Under Solvent-Free Phase Transfer Catalyst Condition, Mustafa Ceylan, Hayretti̇n Gezegen
Preparation Of 1,5-Diketones By Addition Of Cyclohexanone To Chalcones Under Solvent-Free Phase Transfer Catalyst Condition, Mustafa Ceylan, Hayretti̇n Gezegen
Turkish Journal of Chemistry
Eight different chalcone-1,5-diketone derivatives (5a-h) were prepared by the reaction of chalcone derivatives (3a-h) with cyclohexanone under the solvent-free phase transfer catalyst condition with modarate to high yields. The mechanistic pathway of the reaction can be explained by the Michael-type addition of cyclohexanone to chalcone derivatives (3a-h).
The Synthesis And Anticonvulsant Activity Of 1-Substituted-7-Methoxy-1,2,4-Triazolo [4,~3-A]Quinoline, Li-Ping Guan, Xian-Yu Sun, Guan-Rong Tian, Kyu-Yun Chai, Zhe-Shan Quan
The Synthesis And Anticonvulsant Activity Of 1-Substituted-7-Methoxy-1,2,4-Triazolo [4,~3-A]Quinoline, Li-Ping Guan, Xian-Yu Sun, Guan-Rong Tian, Kyu-Yun Chai, Zhe-Shan Quan
Turkish Journal of Chemistry
A new series of 1-substituted-7-methoxy-5-phenyl-1,2,4-triazolo [4,3-a]quinolines were synthesized using ethyl-3-oxo-3-phenylpropanoate and 4-methoxybenzenamine as the starting material. Their anticonvulsant activity was evaluated by the maximal electroshock (MES) test and 7-methoxy-5-phenyl-1,2,4-triazolo[4,3-a]quinoline (4a) was identified as the most potent compound, with an ED_{50} value of 9.2 mg kg^{-1}, which is comparable to the reference drug phenytoin (ED_{50} = 9.9 mg kg^{-1}). To explore the possible mechanism of its anticonvulsant activity, compound 4a was tested with the rotarod neurotoxicity test, pentylenetetrazole (sc-PTZ) test, and isoniazid test. Compound 4a had a higher protective index (PI = TD_{50}/ED_{50}) value (16.6) than phenytoin (PI = 7.0), and …
Synthesis And Characterization Of New Tridentate Iminooxime Ligands And Their Co(Iii) Complexes, Hasene Mutlu, Gazi̇ İrez
Synthesis And Characterization Of New Tridentate Iminooxime Ligands And Their Co(Iii) Complexes, Hasene Mutlu, Gazi̇ İrez
Turkish Journal of Chemistry
In this study, (hydroxyimino)(2-phenyl(1,2,3,4-tetrahydroquinazolin- 2-yl))methane (H_2L^1) and (hydroxyimino)(2-(2-thienyl)(1,2,3,4- tetrahydroquinazolin-2-yl))methane (H_2L^2) were synthesized by the condensation of 2-(hydroxyimino)-1-phenylethan-1-one (INAP) and 2-(hydroxyimino)-1-(2-thienyl)ethan-1-one (INAT) with 2-aminobenzylamine (2-ABA). Complexes of these ligands with Co^{3+} were prepared with a metal:ligand ratio of 1:2. The ligands and their complexes were elucidated on the basis of elemental analyses, AAS, FT-IR, ^1H- and ^{13}C-NMR spectra, mass spectra, magnetic susceptibility measurements, and molar conductivity.
Microwave-Assisted Synthesis Of 1,4´-Diazaflavone And N-Alkyl Derivative Pigments With Anti-Microbial Activity, Nuran Yayli, Osman Üçüncü, Nuretti̇n Yayli, Emi̇ne Demi̇r, Zi̇hni̇ Demi̇rbağ
Microwave-Assisted Synthesis Of 1,4´-Diazaflavone And N-Alkyl Derivative Pigments With Anti-Microbial Activity, Nuran Yayli, Osman Üçüncü, Nuretti̇n Yayli, Emi̇ne Demi̇r, Zi̇hni̇ Demi̇rbağ
Turkish Journal of Chemistry
1,4'-Diazaflavone pigment (2) was synthesized by a simple environmentally friendly microwave-assisted one-pot method for the cyclization of 2'-amino (E)-4''-aza-chalcone (1) under solventless conditions using K-10 clay. In addition, 10 new N-alkyl (C_{5-12, 14-15}) substituted 1,4' -diazaflavonium bromide pigments (3-12) were prepared from compound 2 or directly from compound 1, with corresponding alkyl halides in acetonitrile under reflux. The anti-microbial activity of compounds 1-12 was tested. The N-alkyl substituted 1,4' -diazaflavonium bromides (3-12) showed good antimicrobial activity against the gram-positive bacteria tested with minimal bactericidal concentration (MBC) values for the reference antibiotic kanamycin. The optimum length of the alkyl chain for …