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Full-Text Articles in Physical Sciences and Mathematics
Nucleophilic Substitution Reactions Of Monofunctional Nucleophilic Reagents Withcyclotriphosphazenes Containing 2,2-Dioxybiphenyl Units, Esra Tanriverdi̇ Eçi̇k, Hani̇fe İbi̇şoğlu, Gönül Yeni̇lmez Çi̇ftçi̇, Gi̇zem Demi̇r, Eda Erdemi̇r, Fatma Yüksel
Nucleophilic Substitution Reactions Of Monofunctional Nucleophilic Reagents Withcyclotriphosphazenes Containing 2,2-Dioxybiphenyl Units, Esra Tanriverdi̇ Eçi̇k, Hani̇fe İbi̇şoğlu, Gönül Yeni̇lmez Çi̇ftçi̇, Gi̇zem Demi̇r, Eda Erdemi̇r, Fatma Yüksel
Turkish Journal of Chemistry
The nucleophilic substitution reactions of mono- and bis-spiro-2,2' -dioxybiphenyl cyclotriphosphazenes (3 and 4) with cyclopropanemethylamine (5) and aniline (6) were performed in the presence of trimethylamine in THF. Five novel cyclopropanemethylamino- and anilino-substituted spiro-2,2' -dioxybiphenyl cyclotriphosphazene derivatives (7-11) were obtained from these reactions. The molecular structures of the new cyclotriphosphazene derivatives (7- 11) were characterized by elemental analysis, MALDI-TOF MS, FT-IR, and NMR ( $^{31}$P and $^{1}$H) spectroscopies. The structure of the spiro-(2,2' -dioxybiphenyl)-bis-(anilino)-cyclotriphosphazene (11) was also determined by single-crystal X-ray crystallography.
2-[(3-Aminoalkyl-(Alkaryl-,Aryl-))-1 H-1,2,4-Triazol-5-Yl]Anilines: Synthesis And Anticonvulsant Activity, Yulya Martynenko, Galina Berest, Nina Bukhtiayrova, Igor Belenichev, Oleksiy Voskoboinik, Sergiy Kovalenko
2-[(3-Aminoalkyl-(Alkaryl-,Aryl-))-1 H-1,2,4-Triazol-5-Yl]Anilines: Synthesis And Anticonvulsant Activity, Yulya Martynenko, Galina Berest, Nina Bukhtiayrova, Igor Belenichev, Oleksiy Voskoboinik, Sergiy Kovalenko
Turkish Journal of Chemistry
The presented work is devoted to the development of synthesis methods for novel 2-[(3-aminoalkyl-(alkaryl-, aryl-))-1$H$-1,2,4-triazolo]anilines. Abovementioned compounds were obtained via hydrazinolysis (Ing-Manske procedure) and acid hydrolysis of corresponding $N$-acylated {([1,2,4]triazolo[1,5-$c$]quinazolin-2-yl)alkyl-(alkaryl-, aryl-)} amines. The regioselectivity of hydrazinolysis and hydrolysis were established. The features of spectral characteristics were studied and discussed. Characteristic patterns of protons signals splitting in $^{1}$H NMR of the synthesized compounds were established. The effect of the synthesized compounds on the pentylenetetrazol seizures was studied. It was found that according to some indicators, anticonvulsant activity of 2-[(3-aminoalkyl-(alkaryl-, aryl-))-1$H$-1,2,4-triazolo]anilines superior or comparable with effect of the reference drug "Lamotrigine". It …
Chemical Composition, And Antibacterial And Antioxidant Activities Of Essential Oils From Laggera Tomentosa Sch. Bip. Ex Oliv. Et Hiern (Asteraceae), Tokuma Getahun, Vinit Sharma, Deepak Kumar, Neeraj Gupta
Chemical Composition, And Antibacterial And Antioxidant Activities Of Essential Oils From Laggera Tomentosa Sch. Bip. Ex Oliv. Et Hiern (Asteraceae), Tokuma Getahun, Vinit Sharma, Deepak Kumar, Neeraj Gupta
Turkish Journal of Chemistry
Laggera tomentosa Sch. Bip. ex Oliv. et Hiern (Asteraceae), an endemic Ethiopian medicinal plant, is traditionally used to treat various ailments. Previously, the chemical constituents of the essential oil (EO) of its leaves and inflorescence were documented. However, no data about the chemical compositions of other parts of the EOs of the plant have been reported to date. Moreover, there are no previous biological activity reports on any parts of the EOs of this plant. Thus, in this study, the EOs were isolated from the stem bark and roots of this plant by hydrodistillation and analyzed using gas chromatography-mass spectrometry …