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Full-Text Articles in Physical Sciences and Mathematics
Synthesis Of Some New Isoxazolidines By 1,3-Dipolar Cycloaddition Reaction Of Nitrones And Olefins, Akbar Mobinikhaledi, Naser Forughifar, Zahra Kalate
Synthesis Of Some New Isoxazolidines By 1,3-Dipolar Cycloaddition Reaction Of Nitrones And Olefins, Akbar Mobinikhaledi, Naser Forughifar, Zahra Kalate
Turkish Journal of Chemistry
A series of new isoxazolidines 5a-j were synthesized by 1,3-dipolar cycloaddition reaction of different nitrones with substituted olefins under reflux condition. The yields of products following recrystallization from absolute ethanol were of the order of 40%-66%. IR, NMR and mass spectroscopies were used for identification of these compounds.
Manganese(Iii) Acetate Mediated Free Radical Cyclization Of 1,3-Dicarbonyl Compounds With Sterically Hindered Olefins, Mehmet Yilmaz, Emre Bi̇çer, A. Tarik Pekel
Manganese(Iii) Acetate Mediated Free Radical Cyclization Of 1,3-Dicarbonyl Compounds With Sterically Hindered Olefins, Mehmet Yilmaz, Emre Bi̇çer, A. Tarik Pekel
Turkish Journal of Chemistry
The manganese(III) acetate mediated radical cyclization of dimedone 1a, 2,4-pentanedione 1b, ethyl acetoacetate 1c, 1,3-cyclohexanedione 1d and 5-phenyl-1,3-cyclohexanedione 1e with 1,1-diphenyl-1-butene 2a afforded 4,5-dihydrofurans (3c, 3e) and tetrahydrobenzofurans (3a, 3g, 3h) in good yields (55% - 77%). Additionally, the reactions of trifluoromethyl-group containing 1,3-dicarbonyls, 4,4,4-trifluoro-1-phenylbutane-1,3-dione 1f and 4,4,4-trifluoro-1-thien-2ylbutane-1,3-dione 1g with 2a 3-trifluoroacetyl-4,5-dihydrofurans gave in 74% and 78% yields, respectively. Treatment of 1a, 1b and 1c with 1,2-diphenyl-1-pentene 2a resulted in the formation of tetrahydrobenzofuran 3b and 4,5-dihydrofurans 3d and 3f in lower yields.
Synthesis And Characterization Of New Triheterocyclic Compounds Consisting Of 1,2,4-Triazol-3-One, 1,3,4-Thiadiazole And 1,3,4-Oxadiazole Rings, Nesli̇han Demi̇rbaş
Synthesis And Characterization Of New Triheterocyclic Compounds Consisting Of 1,2,4-Triazol-3-One, 1,3,4-Thiadiazole And 1,3,4-Oxadiazole Rings, Nesli̇han Demi̇rbaş
Turkish Journal of Chemistry
A series of acetic acid derivatives (2a-c) was synthesized by the condensation of compounds 1a-c with chloroacetic acid. The treatment of carboxylic acid derivatives with thiosemicarbazide in phosphorus oxychloride and subsequent diazotation of the products (3a-c) afforded 5-alkyl-2-[(5-chloro-1,3,4-thiadiazol-2-yl)methyl]- 2,4-dihydro-3H-1,2,4-triazol-3-one derivatives (4a-c). The treatment of compounds 4a-c with thiourea produced 5-alkyl-2-[(5-mercapto-1,3,4- thiadiazol-2-yl)methyl]-2,4-dihydro-3H-1,2,4-triazol-3-one derivatives (5a-c). Subsequently, compounds 5a-c were converted to acid hydrazides by treatment with hydrazine hydrate after esterification (7a-e). Moreover, the reaction of compounds 7a-c with carbon disulfite in the presence of KOH afforded 5-alkyl-2-[(5-\{[(5- mercapto-1,3,4-oxadiazol-2-yl)methyl]thio\}-1,3,4-thiadiazol-2-yl)methyl]- 2,4-dihydro-3H-1,2,4-triazol-3-ones (8a-c).