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Full-Text Articles in Chemistry
Synthesis And In Vitro Anti-Helicobacter Pylori Activity Of 2-(Substituted Benzylthio)-5-(5-Nitro-2- Furyl)-1, 3, 4-Thiadiazole Derivatives, Negar Mohammadhosseini, Ali Asadipor, Bahram Letafat, Mohsen Vosooghi, Farideh Siavoshi, Abbas Shafiee, Alireza Foroumadi
Synthesis And In Vitro Anti-Helicobacter Pylori Activity Of 2-(Substituted Benzylthio)-5-(5-Nitro-2- Furyl)-1, 3, 4-Thiadiazole Derivatives, Negar Mohammadhosseini, Ali Asadipor, Bahram Letafat, Mohsen Vosooghi, Farideh Siavoshi, Abbas Shafiee, Alireza Foroumadi
Turkish Journal of Chemistry
Starting from (5-nitrofuran-2-yl)methylene diacetate, a new series of 2-[(substituted benzyl)thio]-5-(5-nitro-2-furyl)-1,3,4-thiadiazoles (6a-n) were synthesized and the structures of the compounds were determined using spectroscopic methods including mass spectrometry, ^1H-nuclear magnetic resonance, infrared spectroscopy, and elemental analysis. The in vitro anti-Helicobacter pylori activity of the synthesized compounds was evaluated by the disk diffusion method against the clinical isolates of Helicobacter pylori. The results indicated that most of the synthesized compounds exhibited significant inhibitory activity against H. pylori with respect to standard drug metronidazole. Compound 6l, containing the 2-chloro-6-fluorobenzylthio moiety, was the most potent compound tested.
Synthesis And In Vitro Anti-Helicobacter Pylori Activity Of 2-(Substituted Benzylthio)-5-(5-Nitro-2- Furyl)-1, 3, 4-Thiadiazole Derivatives, Hossein Nasr Isfahani, Khalil Faghihi, Atena Izadkhah, Meisam Shabanian
Synthesis And In Vitro Anti-Helicobacter Pylori Activity Of 2-(Substituted Benzylthio)-5-(5-Nitro-2- Furyl)-1, 3, 4-Thiadiazole Derivatives, Hossein Nasr Isfahani, Khalil Faghihi, Atena Izadkhah, Meisam Shabanian
Turkish Journal of Chemistry
Starting from (5-nitrofuran-2-yl)methylene diacetate, a new series of 2-[(substituted benzyl)thio]-5-(5-nitro-2-furyl)-1,3,4-thiadiazoles (6a-n) were synthesized and the structures of the compounds were determined using spectroscopic methods including mass spectrometry, ^1H-nuclear magnetic resonance, infrared spectroscopy, and elemental analysis. The in vitro anti-Helicobacter pylori activity of the synthesized compounds was evaluated by the disk diffusion method against the clinical isolates of Helicobacter pylori. The results indicated that most of the synthesized compounds exhibited significant inhibitory activity against H. pylori with respect to standard drug metronidazole. Compound 6l, containing the 2-chloro-6-fluorobenzylthio moiety, was the most potent compound tested.
A Highly Soluble Asymmetric Perylene-Bis (Dicarboximide)-Acceptor System Incorporating A Methylene Bridged Methoxybenzene-Donor: Solvent Dependence Of Charge Transfer Interactions, Rene M. Williams
Turkish Journal of Chemistry
The synthesis and photophysical properties of an asymmetrically substituted perylene-bis(dicarboximide), (PDI), system (1) containing a methylene bridged 4-methoxy-benzene donor and a solubilizing branched C_{13} alkyl chain are described. As compared to most PDIs, the fluorescence of 1 is strongly quenched in polar (but not in non-polar) solvents due to a photo-induced electron transfer process. Transient absorption spectroscopy and time resolved emission in e.g. acetonitrile indicates that upon excitation the radical anion of the PDI is formed with a rate of ca. 3.5 \times 10^9s^{-1}, and the charge transfer state has a lifetime of ca. 3 ns. A Frontier Molecular Orbital …
Synthesis, Characterization, And Optical Properties Of Novel 2,5-Bis[4-(2-(-Arylvinyl)Phenyl]-1,3,4-Oxadiazoles, Dao-Hang He, Yong-Chuang Zhu, Zhuo-Ru Yang, Ai-Xi Hu, Gao Cao
Synthesis, Characterization, And Optical Properties Of Novel 2,5-Bis[4-(2-(-Arylvinyl)Phenyl]-1,3,4-Oxadiazoles, Dao-Hang He, Yong-Chuang Zhu, Zhuo-Ru Yang, Ai-Xi Hu, Gao Cao
Turkish Journal of Chemistry
Six novel 2,5-bis[4-(2-arylvinyl)phenyl]-1,3,4-oxadiazoles were synthesized by introducing 1,3,4-oxadiazole moiety into the stilbene skeleton. The synthesis route included the cyclization of p-toluic acid and hydrazine hydrate catalyzed by polyphosphoric acid (PPA), bromination of 1,3-dibromo-5,5-dimethylhydantoin (DBDMH), esterification, and the Wittig-Horner reaction. All the title compounds were characterized by ^1H-NMR, MS, and elemental analysis. UV-Vis absorption and fluorescence emission spectra in THF solution were investigated; the compounds may have potential for use in organic optical materials.