Open Access. Powered by Scholars. Published by Universities.®
Physical Sciences and Mathematics Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 4 of 4
Full-Text Articles in Physical Sciences and Mathematics
Synthesis And Antiinflammatory Activity Of Novel 2,5-Disubstituted Thiophene Derivatives, Sahar Badr
Synthesis And Antiinflammatory Activity Of Novel 2,5-Disubstituted Thiophene Derivatives, Sahar Badr
Turkish Journal of Chemistry
New series of 2,5-disubstituted thiophenes were synthesized. Thiosemicarbazones 1a-b were reacted with various reagents, such as diethyl-2-bromomalonate, ethyl-2-chloroacetoacetate, thioglycolic acid, 4-substituted phenacyl bromides, and acetic anhydride, to afford heterocyclic substituted thiophene derivatives 2a-b, 3a-b, 4a-b, 5a-b, 6a-b, and 7a-b, respectively. Moreover, cyclization of the key intermediate 1b with chloroacetic acid yielded thiazolidine 9, which on reaction with appropriate aromatic aldehydes afforded the corresponding arylidene derivatives 10a-f. Finally, reaction of N^\-arylidene cyanoacetohydrazide 11 with sulfur and phenylisothiocyanate yielded thiazoline derivative 12, which on treatment with triethylorthoformate and acetic anhydride afforded thiazolo[4,5-d]pyrimidinone derivative 13. Some of the newly synthesized compounds showed promising …
Synthesis, Crystal Structure, And Antioxidant Properties Of Novel 1,2,4-Triazol-5-Ones Containing 3,4-Dimethoxyphenyl And 3,4-Dihydroxyphenyl Moiety, Yasemi̇n Ünver, Sevgi̇ Meydanal, Kemal Sancak, Di̇lek Ünlüer, Reşat Ustabaş, Esra Düğdü
Synthesis, Crystal Structure, And Antioxidant Properties Of Novel 1,2,4-Triazol-5-Ones Containing 3,4-Dimethoxyphenyl And 3,4-Dihydroxyphenyl Moiety, Yasemi̇n Ünver, Sevgi̇ Meydanal, Kemal Sancak, Di̇lek Ünlüer, Reşat Ustabaş, Esra Düğdü
Turkish Journal of Chemistry
A series of new 4-(3,4-dimethoxyphenethyl)-5-akyl/aryl-2H- 1,2,4-triazol-3(4H)-ones (3a-g) was obtained by the reaction of ethyl 2-(ethoxy)(alkylidene/arylidene)hydrazinecarboxylate (1) and 2-(3,4-dimethoxyphen- yl)ethanamine (2). Compounds 4a-f and 5 were synthesized from the reaction of corresponding compounds 3a-f and 3g with BBr_3, respectively. With elemental analysis, IR, ^1H-NMR, and ^{13C-NMR spectral data, 14 newly synthesized compounds were characterized. The structure of compound 3a was inferred through IR, ^1H- and ^{13}C-NMR, elemental analysis, and X-ray spectral techniques. In addition, the newly synthesized chemicals were screened for their antioxidant properties. Among the chemicals tested, 4a, 4c, 4d, 4f, and 5 exhibited the highest degree of antioxidant activity.
Synthesis And Characterization Of New Symmetrical 3,6-Bis[(25,26,27- Tripropoxy-28-(3-(4-Iodophenyl) Propoxy)-P-Tert-Butyl Calix[4]Arene Ethynyl]-9h- Fluoren-9-One By Sonogashira Coupling As A Novel Precursor For Synthesis Of Quinodimethane (Qdm), Karim Akbari Dilmaghani, Fazel Nasuhi Pur
Synthesis And Characterization Of New Symmetrical 3,6-Bis[(25,26,27- Tripropoxy-28-(3-(4-Iodophenyl) Propoxy)-P-Tert-Butyl Calix[4]Arene Ethynyl]-9h- Fluoren-9-One By Sonogashira Coupling As A Novel Precursor For Synthesis Of Quinodimethane (Qdm), Karim Akbari Dilmaghani, Fazel Nasuhi Pur
Turkish Journal of Chemistry
Novel symmetrical 3,6-bis[(25,26,27-tripropoxy-28-(3-(4-iodophenyl)propoxy)-p-tert-butyl calix[4]arene ethynyl]-9H-fluoren-9-one with a cone conformation was synthesized by palladium-catalyzed coupling of (25,26,27-tripropoxy- 28-(3-(4-iodophenyl)propoxy)-p-tert-butyl calix[4]arene and 3,6-diethynyl-9H-fluoren-9-one. Its structure was confirmed by FT-IR, ^1H-NMR, and ^{13}C-NMR spectroscopy, and elemental analysis and positive ion FAB mass spectrometry.
Chemistry Of Dibenzobarallene, Moustafa A. Gouda, Moged A. Berghot, Khaled M. Elattar, Abd El Galil M. Khalil
Chemistry Of Dibenzobarallene, Moustafa A. Gouda, Moged A. Berghot, Khaled M. Elattar, Abd El Galil M. Khalil
Turkish Journal of Chemistry
This review represents a systematic and comprehensive survey of the methods of syntheses and chemical reactivity of dibenzobarallene. This compound is an important intermediate for the synthesis of useful and novel heterocycle systems.