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Full-Text Articles in Physical Sciences and Mathematics
Oxidative Cyclisation Of 3-Oxopropanenitriles Mediated Manganese(Iii) Acetate With 2-Thienyl Substituted Alkenes, Mehmet Yilmaz, Neşe Uzunali̇oğlu, Mehtap Yakut, A. Tarik Pekel
Oxidative Cyclisation Of 3-Oxopropanenitriles Mediated Manganese(Iii) Acetate With 2-Thienyl Substituted Alkenes, Mehmet Yilmaz, Neşe Uzunali̇oğlu, Mehtap Yakut, A. Tarik Pekel
Turkish Journal of Chemistry
The oxidative cyclisation of 3-oxopropanenitriles 1a-g with alkenes 2a-c containing 2-thienyl group by manganese(III) acetate was studied. Treatment of 3-oxopropanenitriles 1a-d with 2-[(E)-2-phenylvinyl] thiophene 2a gave 4-phenyl-5-(2-thienyl)-4,5-dihydrofuran-3-carbonitriles 3a-d in moderate yields (52%-60%). 5-(2-thienyl) substituted 4,5-dihydrofuran-3-carbonitriles 3e-i were obtained by the oxidative cyclisation of these 3-oxopropanenitriles with 2-[(E)-1-methyl-2- phenylvinyl]thiophene 2b in good yields (54%-68%). In addition, the reactions of 2-(1-phenylvinyl)thiophene 2c with various 3-oxopropanenitriles produced 4,5-dihydrofurans 3j-n containing heterocycle in 77%-91% yields.
Preparation, Characterization, And Potentiometric Titrations Of Some New Di-[3-(3-Alkyl/Aryl-4,5-Dihydro-1h-1,2,4-Triazol-5-One-4-Yl)-Azomethinphenyl] Isophthalate/Terephthalate Derivatives, Haydar Yüksek, Özlem Gürsoy Kol
Preparation, Characterization, And Potentiometric Titrations Of Some New Di-[3-(3-Alkyl/Aryl-4,5-Dihydro-1h-1,2,4-Triazol-5-One-4-Yl)-Azomethinphenyl] Isophthalate/Terephthalate Derivatives, Haydar Yüksek, Özlem Gürsoy Kol
Turkish Journal of Chemistry
3-Alkyl(Aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) reacted with di-(3-formylphenyl) isophthalate (3) and di-(3-formylphenyl) terephthalate (6) to afford the corresponding 6 novel di-[3-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)- azomethinphenyl] isophthalates (4) and 6 novel di-[3-(3-alkyl/aryl-4,5- dihydro-1H-1,2,4-triazol-5-one-4-yl)-azomethinphenyl] terephthalates (7), respectively. The acetylation reactions of compounds 4 and 7 were investigated, and 5 and 8 type compounds were obtained, respectively. The new compounds synthesized were characterized by using IR, ^1H-NMR, ^{13}C-NMR, and UV spectral data together with elemental analysis. In addition, to investigate the effects of solvents and molecular structure upon acidity, compounds 4 and 7 were titrated potentiometrically with tetrabutylammonium hydroxide in 5 non-aqueous solvents (isopropyl alcohol, tert-butyl alcohol, N,N-dimethylformamide, acetone, …