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Articles 1 - 3 of 3
Full-Text Articles in Physical Sciences and Mathematics
Synthesis Of The Novel Benzothiazole Compounds From 7-Benzylidenebicyclo [3.2.0] Hept-2-En-6-Ones And 2-Aminobenzenethiol, Esra Findik
Turkish Journal of Chemistry
Synthesis of the 2-(2-styrylcyclopent-3-enyl)benzo-[d]thiazoles (6a-i) is reported for the first time. Reaction of 7-benzylidenebicyclo [3.2.0] hept-2-en-6-ones (3a-i) and 2-aminobenzenethiol (4) in the presence of p-TsOH as a catalyst, in ethanol under reflux, resulted in the formation of novel 2-(2-styrylcyclopent-3-enyl)benzo[d]thiazoles in high yields.
Synthesis, Characterization, And Antioxidant Activities Of New Trisubstituted Triazoles, Kemal Sancak, Yasemi̇n Ünver, Di̇lek Ünlüer, Esra Düğdü, Gülcan Kör, Fati̇h Çeli̇k, Emrah Bi̇ri̇nci̇
Synthesis, Characterization, And Antioxidant Activities Of New Trisubstituted Triazoles, Kemal Sancak, Yasemi̇n Ünver, Di̇lek Ünlüer, Esra Düğdü, Gülcan Kör, Fati̇h Çeli̇k, Emrah Bi̇ri̇nci̇
Turkish Journal of Chemistry
A series of new 4-(3,4dimethoxyphenethyl)-3,5-akyl/aryl-4H- 1,2,4-triazoles (3a-g) were obtained by reaction of ethyl N'-(alkylidene/arylidene)hydrazonate (1) and 2-(3,4-dimethoxy phenyl)ethanamine (2). Compounds 4d, e, and g were synthesized from the reaction of corresponding compounds 3d, e, and g with BBr_3, respectively. The 10 new compounds synthesized were characterized by elemental analyses, IR, ^1H-NMR, and ^{13}C-NMR spectral data. The structure of compound 3g was inferred through IR, ^1H-, ^{13}C-NMR, elemental analyses, and X-ray spectral techniques. In addition, the newly synthesized chemicals were screened for their antioxidant properties. Among the chemicals tested, 4d, e, and g exhibited the highest degree of antioxidant activity.
Synthesis Of 3-Pyrroline-2-Ones From Amino Acids And An Aryl Amine, Nezi̇re Saygili, Cemi̇l Aydoğan
Synthesis Of 3-Pyrroline-2-Ones From Amino Acids And An Aryl Amine, Nezi̇re Saygili, Cemi̇l Aydoğan
Turkish Journal of Chemistry
The conversion of the amino group of amino dicarboxylicacid esters and an aryl amine into N-substituted pyrrolinone derivatives with dimethoxydihydrofurane is described. The conversion also occurs with serine methylester but it decomposes very quickly.