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11.
Thiosemicarbazides of 2-hydroxyphenylglyoxylic acid, which, depending on the conditions, undergo cyclization to interconvertible 5-(2-hydroxyphenyl)-6-oxo-1,2,4-triazine-3-thiones or (2-hydroxy-benzoyl)-2-1,2,4-triazoline-5-thiones, are formed by the action of thiosemicarbazide and its homologs on coumarindione. The thiosemicarbazones of 2-hydroxyphenylglyoxlyic and other 2-substituted phenylglyoxylic acids undergo cyclization to 6-(2-hydroxyphenyl)-5-oxo-1,2,4-triazine-3-thiones.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp, 116–121, January, 1977.  相似文献   
12.
Reactions of acetylthioacetanilide with arylamines in acetic acid in the presence of sodium acetate give 3-arylaminothiocrotonanilides in good yields. When treated with -bromoacetophenone in acetone, these products are converted to substituted 4-hydroxy-2-thiazolinium bromides, one of which was dehydrated to obtain the corresponding thiazolium bromide. The structure of the heterocyclization products was confirmed by single crystal X-ray diffraction and NMR study of 2-acetonylidene-3,4-diphenyl-2,3-dihydrothiazole formed by dehydration of the corresponding 2-thiazolinium salt with simultaneous hydrolysis.  相似文献   
13.
We establish conditions under which the integral of a function along a nilpotent flow on the Heisenberg-Iwasawa manifold increases not faster than and indicate cases where this integral can be represented as a superposition of a function defined on a nilmanifold and a nilpotent flow.Translated from Ukrainskii Matematicheskii Zhurnal, Vol. 47, No. 6, pp. 837–847, June, 1995.  相似文献   
14.
We establish sufficient conditions for a nonlinear system of difference equations x(t + 1) =x(t) + + P(x(t),t)+ to be reducible to the system y(t + 1) =y(t) + . Here, P(x, t) is a function 2-periodic in xi(i = 1, ...,n) and almost periodic int with a frequency basis .Translated from Ukrainskii Matematicheskii Zhurnal, Vol. 46, No. 4, pp. 404–412, April, 1994.This work was supported by Ukrainian State Committee on Science and Technology.  相似文献   
15.
The possibility of modifying boron polyoxide with an oligomeric amide upon thermal dehydration of orthoboric acid and oligomerization of caprolactam in a common melt is shown. The products obtained after thermal pretreatment of the initial blend containing 30 wt % caprolactam are investigated. It is shown that the main processes at T < 200°C are dehydration of orthoboric acid and hydrolysis of caprolactam with the formation of ε-aminocaproic acid. At temperatures of 225–260°C, the predominant process is the formation of boron polyoxide and a caprolactam-based oligomeric product. The data of 11B NMR spectroscopy show that the chemical transformations of caprolactam occur against the background of the N:B donor-acceptor interaction. The two-dimensional [11B-1H] heteronuclear correlation spectrum indicates that the systems obtained upon thermal treatment are solid solutions.  相似文献   
16.
Russian Journal of General Chemistry - The action of sulfur diethylaminotrifluoride on 19β,28-epoxyoleanan-3-ol (allobetulin) causes dehydration of the terpenoid and isomerization of the ring...  相似文献   
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A model of the process of methane delivery from seafloor deposits of solid hydrates to the surface has been developed and approved. The model considers methane delivery through a vertical pipe lowered from the sea surface to the seafloor deposit. The model allows to determine important characteristics of the flow through the pipe—the possibility of stationary self-sustained flow of the medium to the surface; the gushing character of the flow; medium velocity, pressure, and composition distribution along the pipe—and thus to optimize the process of gas production.  相似文献   
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The polymerization of 1-butene over the TiCl4/MgCl2 (TMC) catalyst with the use of substituted phosphine oxides R n P(O)(CH2OR′)3 ? n (R = alkyl, R′ = methyl or acyl, n = 0–2)—new external electron donors-has been investigated. The electron-donating (coordinating) centers in these compounds are the phosphoryl group (P=O) and the oxygen atoms of the substituents at the phosphorus atom. The dependence of the 1-butene polymerization activity of TMC on the nature of the substituents in the phosphine oxides has been studied. The microstructure, degree of crystallinity, molecular weight, and strain-strength characteristics of the synthesized polybutene-1 and the effect of hydrogen on these properties are reported. The most efficient external donor is Me2P(O)CH2OAc.  相似文献   
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