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Articles 1 - 7 of 7
Full-Text Articles in Physical Sciences and Mathematics
A New And Convenient Method Of Generating Alkyl Isocyanates From Alcohols, Thiols, And Trimethylsilyl Ethers Using A 2,4,6-Trichloro[1,3,5] Triazine/N-Bu_4nocn, Batool Akhlaghinia, Sima Samiei
A New And Convenient Method Of Generating Alkyl Isocyanates From Alcohols, Thiols, And Trimethylsilyl Ethers Using A 2,4,6-Trichloro[1,3,5] Triazine/N-Bu_4nocn, Batool Akhlaghinia, Sima Samiei
Turkish Journal of Chemistry
Alkyl isocyanates are prepared in good to excellent yields by treatment of alcohols, thiols, and trimethylsilyl ethers with 2,4,6-trichloro[1,3,5] triazine/n-Bu_4NOCN in acetonitrile. This method is highly selective for conversion of 1° alcohols to alkyl isocyanates in the presence of 2° and 3° alcohols, thiols, and trimethylsilyl ethers.
Efficient Method For Tetrahydropyranylation Of Phenols And Alcohols Using 2,4,6-Trichloro[1,3,5]Triazine, Batool Akhlaghinia, Elham Roohi
Efficient Method For Tetrahydropyranylation Of Phenols And Alcohols Using 2,4,6-Trichloro[1,3,5]Triazine, Batool Akhlaghinia, Elham Roohi
Turkish Journal of Chemistry
Alcohols and phenols were tetrahydropyranylated in the presence of 2,4,6-trichloro[1,3,5]triazine in good to excellent yields in acetonitrile.
Synthesis Of Nitrogen-Containing Heterocycles From The Reaction Of Amidrazones With \Alpha-Haloesters, Hany M. Dalloul, Peter H. Boyle
Synthesis Of Nitrogen-Containing Heterocycles From The Reaction Of Amidrazones With \Alpha-Haloesters, Hany M. Dalloul, Peter H. Boyle
Turkish Journal of Chemistry
The reaction of amidrazones 1 with \alpha-haloesters 2 formed 1,3,5-substituted 4,5-dihydro-1,2,4-triazin-6-ones (4a-z) rather than 1,2,4-triazin-5-one derivatives (5a-z). The microanalysis and spectral data of the synthesized compounds are in full agreement with their molecular structure.
Synthesis And Physico-Chemical And Spectroscopic Investigations Of Sodium Dihydrobis(1,2,3-Benzotriazolyl)Borate Ligand And Its Transition Metal Complexes, . Lutfullah, Ahmad Umar, Mohammed Muzibur Rahman, Mohammad Mansoob Khan, Yoon Bong Hahn
Synthesis And Physico-Chemical And Spectroscopic Investigations Of Sodium Dihydrobis(1,2,3-Benzotriazolyl)Borate Ligand And Its Transition Metal Complexes, . Lutfullah, Ahmad Umar, Mohammed Muzibur Rahman, Mohammad Mansoob Khan, Yoon Bong Hahn
Turkish Journal of Chemistry
The title ligand, sodium dihydrobis(1,2,3-benzotriazolyl)borate, Na[H_2B(BTz)_2], was synthesized by refluxing 1 mole of sodium borohydride with 2 moles of 1,2,3- benzotriazole in toluene. The ligand shows ample reactivity towards Cr(III), Mn(II), Fe(III), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II) metal ions and forms stable complexes. The ligand and its metal complexes were characterized by physico-chemical and spectroscopic techniques. All the complexes of divalent metal ions are tetrahedral except for Cu(II), which has been proposed to have a square-planar geometry. The complexes of Cr(III) and Fe(III) appear to have an octahedral geometry. The magnitude of molar conductance of 10^{-3} M …
Synthesis Of Some New 1-Acylthiosemicarbazides And 1,2,4-Triazol-5-Thiones, And Their Analgesic And Anti-Inflammatory Activities, Yasemi̇n Dündar, Bi̇lge Çakir, Esra Küpeli̇, M. Fethi̇ Şahi̇n, Ni̇ngur Noyanalpan
Synthesis Of Some New 1-Acylthiosemicarbazides And 1,2,4-Triazol-5-Thiones, And Their Analgesic And Anti-Inflammatory Activities, Yasemi̇n Dündar, Bi̇lge Çakir, Esra Küpeli̇, M. Fethi̇ Şahi̇n, Ni̇ngur Noyanalpan
Turkish Journal of Chemistry
We synthesized new 1-[3-(2-oxobenzothiazolin-3-yl)propanoyl]-4- substituted-thiosemicarbazides and their corresponding cyclized 3-[2-(2-oxobenzothiazoline-3-yl)ethyl]-4-substituted-1,2,4-triazol-5-thione ana-logs in which position 4 of the triazole ring was substituted by cyclohexyl, methyl, allyl, phenyl, p-methylphenyl, p-methoxyphenyl, p-chlorophenyl, p-nitrophenyl, benzyl, and phenylethyl to screen their analgesic and anti-inflammatory activities as well as gastric ulceration potential in test animals. None of the compounds, except 5a, 5e, and 5h, caused gastric lesions or bleeding. Compound 5g was found to have higher analgesic and anti-inflammatory activity among the synthesized compounds.
Synthesis Of Some Novel 3,5-Diaryl-1,2,4-Triazole Derivatives And Investigation Of Their Antimicrobial Activities, Mevlut Serdar, Nurhan Gümrükçüoğlu, Şengül Alpay Karaoğlu, Nesli̇han Demi̇rbaş
Synthesis Of Some Novel 3,5-Diaryl-1,2,4-Triazole Derivatives And Investigation Of Their Antimicrobial Activities, Mevlut Serdar, Nurhan Gümrükçüoğlu, Şengül Alpay Karaoğlu, Nesli̇han Demi̇rbaş
Turkish Journal of Chemistry
A series of acylhydrazones (2a-d) was synthesized from the reactions of iminoester hydrochlorides (1a-e) with acyl hydrazines. 2,5-Dialkyl 1,3,4-oxadiazoles (3a-d) were obtained in the same reaction media. The treatment of acylhydrazones with hydrazine hydrate afforded 4-amino-3,5-dialkyl-1,2,4-triazoles (4a-c). The acetylation of 4-amino-3-(4-hydroxyphenyl)-5-phenyl-4H-1,2,4-triazole (4a) produced 4-amino-5-(4-acetoxyphenyl)-3-phenyl-4H-1,2,4-triazole (9), while the acetylation of 4-amino-3-(4-tolyl)-5-phenyl-4H-1,2,4-triazole (4b) gave 4-acetylamino-3-phenyl-5-(4-tolyl)-4H-1,2,4-triazole (10). The treatment of compound 4b with various aromatic aldehydes or acetophenone and 4-nitroacetophenone resulted in the formation of 4-arylidenamino-3,5-dialkyl-4H-1,2,4-triazoles (5a-e and 7a,b). Sodium borohydride reduction of 4-arylidenamino derivatives of 1,2,4-triazoles afforded 4-alkylamino-3,5-dialkyl-4H-1,2,4-triazoles (6a-e and 8a,b). All newly synthesized compounds were screened for their antimicrobial and antifungal …
Synthesis And Antimicrobial Activities Of Some New 1,2,4-Triazole Derivatives, Nurhan Gümrükçüoğlu, Mevlut Serdar, Eli̇f Çeli̇k, Ali̇ Sevi̇m, Nesli̇han Demi̇rbaş
Synthesis And Antimicrobial Activities Of Some New 1,2,4-Triazole Derivatives, Nurhan Gümrükçüoğlu, Mevlut Serdar, Eli̇f Çeli̇k, Ali̇ Sevi̇m, Nesli̇han Demi̇rbaş
Turkish Journal of Chemistry
A series of acylhydrazones (2a-f) were synthesized by the condensation of iminoester hydrochlorides (1a-f) with acyl hydrazines. 2,5-Dialkyl 1,3,4-oxadiazoles (3a,c,e) were obtained in the same reaction media. The treatment of acylhydrazones with hydrazine hydrate afforded 4-amino-3,5-dialkyl-1,2,4-triazoles (4a-c). The acetylation of 4-amino-3,5-dialkyl-1,2,4-triazoles produced N-[3,5-dialkyl-4H-1,2,4-triazol-4-yl] acetamides (5-7). The treatment of compounds 4a and 4c with various aromatic aldehydes resulted in the formation of 4-arylidenamino-3,5-dialkyl-1,2,4-triazoles (8a,d, e, and 10a-e). Sodium borohydride reduction of 4-arylidenamino derivatives afforded 4-alkylamino-3,5-dialkyl-1,2,4-triazoles (9a,d, e, and 11a-e). Compounds 4b, 4c, 7, 8d, and 11c showed good antifungal activity only against yeast-like fungi, while compounds 3e, 6, 8e, and 9e …