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 Найдено в других БД:Публикации Чарушина В.Н. (17)
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1.
Инвентарный номер: нет.
   
   D 49


   
    Development of certified reference samples of solutions of trihalomethanes [Electronic resource] / V. E. Kirichenko, M. G. Pervova, K. I. Pashkevich, I. A. Piterskikh // Journal of Analytical Chemistry. - 2000. - Vol. 55, N 3. - P221-226
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

\\\\Expert2\\nbo\\Journal of Analytical Chemistry\\2000, V. 55, N 3, p. 221.pdf
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2.
Инвентарный номер: нет.
   
   C 41


   
    Certified reference samples of tetrachloromethane, tetrachloroethylene, and chlorophenol solutions [Electronic resource] / I. A. Piterskikh, V. E. Kirichenko, M. G. Pervova, K. I. Pashkevich // Journal of Analytical Chemistry. - 2000. - Vol. 55, N 3. - P227-230
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

\\\\Expert2\\nbo\\Journal of Analytical Chemistry\\2000, V. 55, N 3, p. 227.pdf
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3.
Инвентарный номер: нет.
   
   K 48


    Kirichenko, V. E.
    The comparsion of approaches for determinations of phenols as derivatives [Text] : доклад, тезисы доклада / V. E. Kirichenko, M. G. Pervova, K. I. Pashkevich // International Congress of Analitical Chemistry, M., June 15-21, 1997 : absracts. - M., 1997. - Vol. 1. - PE89
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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4.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of 2,3-bis(perfluoroalkyl)quinoxalines and 2,3-bis(perfluoroalkyl)-1,4-benzoxazines from oxides of internal perfluoroolefins [Electronic resource] / L. V. Saloutina, A. Ya. Zapevalov, V. I. Saloutin, M. I. Kodess, V. E. Kirichenko, M. G. Pervova, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2005. - Vol. 126, № 6. - P976-983
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of oxides of internal trans-, cis-perfluoroolefins with o-phenylenediamine and 2-aminophenol in dioxane gave 2,3-bis(perfluoroalkyl)quinoxalines and 2,3-bis(perfluoroalkyl)-2H-1,4-benzoxazin-2-ols respectively in yields of 23–67%. When N,N-dimethylacetamide was used as a solvent an anionic isomerization of the oxides into ketones, which further yielded 2-(perfluoroalkyl)benzimidazoles in the case of o-phenylenediamine and 2-hydroxy-N-perfluoroalkanoylanilines in the case of 2-aminophenol, became the main path of these reactions. Unusual cyclization resulting in 2-pentafluoroethyl-2-pentafluoropropanoylbenzoxazolidine occurs on interaction between dodecafluoro-3,4-epoxyhexane and 2-aminophenol in N,N-dimethylacetamide.

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2005, v.126, p.976.pdf
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5.
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   R 30


   
    Reactivity of congeners of Sovol technical mixture of polychlorinated biphenyls toward sodium methoxide [Electronic resource] / O. N. Zabelina, T. I. Gorbunova, M. G. Pervova, V. E. Kirichenko, A. Ya. Zapevalov, V. I. Saloutin, O. N. Chupakhin // Russian Journal of Applied Chemistry. - 2004. - Vol. 77, № 9. - P1523-1527. - Библиогр. : с. 1527 (6 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reaction of Sovol technical mixture of polychlorobiphenyls with sodium methoxide in bipolar aprotic solvents was studied. The reactivity of polychlorobiphenyls was evaluated using gas chromatography and gas chromatography-mass spectrometry.

\\\\Cserver\\dist\\НБО\\Электронная библиотека_Библиогр1\\Russian Journal of Applied Chemistry\\2004, v. 77, N. 9 p.1523.pdf
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6.
Инвентарный номер: нет.
   
   A 10


   
    A route to fluorocontaining N,S-heterocycles via octafluoro-2,3-epoxybutane [Text] / L. V. Saloutina, A. Ya. Zapevalov, V. I. Saloutin, P. A. Slepukhin, M. I. Kodess, V. E. Kirichenko, M. G. Pervova, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2007. - Vol. 128, № 7. - P769-778
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reaction of octafluoro-2,3-epoxybutane 1 with 2-aminothiophenol gave three kinds of novel fluorocontaining N,S-heterocyclic compounds depending on the solvent nature: 2,3-bis(trifluoromethyl)-3,4-dihydro-2H-1,4-benzothiazin-2-ol 2, 2-trifluoromethyl-2-[1-(2-aminophenylthio)-2,2,2-trifluoroethyl]-1,3-benzothiazolidine 6 and 5a,11a-bis(trifluoromethyl)-5a,6,11a,12-tetrahydro-5,11-dithia-6,12-diazanaphthacene 5. Use of the toluene, dioxane, tetrahydrofuran, acetonitrile and dimethoxyethane gave the unexpected dihydrobenzothiazine 2 (RS,SR RR,SS) in good to moderate yields. In dimethylsulfoxide and N,N-dimethylacetamide, unusual cyclization occurred resulting in benzothiazolidine 6 (RS,SR/RR,SS 1:1) in moderate yields. Formation of minor 1,1,1,3,4,4,4-heptafluoro-3-(2-aminophenylthio)-2,2-dihydroxybutane 4 which was converted into bis(benzothiazine) 5 was observed in all solvents tested with the exception of toluene and dioxane. The molecular structure of the RS,SR-diastereomer of dihydrobenzothiazine 2, bis(benzothiazine) 5 and the RS,SR-diastereomer of benzothiazolidine 6 has been established by X-ray crystallography.

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2007, v.128. p.769.pdf
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7.
Инвентарный номер: нет.
   
   R 30


   
    Reaction of 2,3-epoxyoctafluorobutane with 2-aminobenzenethiol [Electronic resource] / L. V. Saloutina, A. Ya. Zapevalov, V. I. Saloutin, M. I. Kodess, V. E. Kirichenko, M. G. Pervova, O. N. Chupakhin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2006. - Vol. 42, № 9. - P1307-1312. - Bibliogr. : p. 1312 (13 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
2,3-EPOXYOCTAFLUOROBUTANE -- 2-AMINOBENZENETHIOL -- EPOXY RING
Аннотация: The reaction of 2,3-epoxyoctafluorobutane with 2-aminobenzenethiol in N,N-dimethylacetamide gave 3-(2-aminophenylsulfanyl)-1,1,1,3,4,4,4- heptafluorobutane-2,2-diol. In the reaction of the same compounds in dioxane, 2,3-bis(trifluoromethyl)-3,4-dihydro-2H-1,4-benzothiazin-2-ol was formed as a result of primary attack by the amino group in 2-aminobenzenethiol on the epoxy ring. The same product was obtained by treatment with 2-aminobenzenethiol of 2,3-bis(trifluoromethyl)-2H-1,4-benzoxazin-2-ol which was synthesized from 2,3-epoxyoctafluorobutane and 2-aminophenol.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2006, 42 (9), 1307.pdf
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8.
Инвентарный номер: нет.
   
   P 93


   
    Products of the reaction of polychlorinated biphenyls with ethanol and potassium hydroxide in dimethyl sulfoxide [Electronic resource] / O. N. Zabelina, V. E. Kirichenko, M. G. Pervova, Yu. G. Yatluk, V. I. Saloutin // Russian Journal of Applied Chemistry. - 2006. - Vol. 79, № 5. - P791-798. - Bibliogr. : p. 798 (8 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BIPHENYLS -- ETHANOL -- POTASSIUM HYDROXIDE -- DIMETHYL SULFOXIDE -- GAS CHROMATOGRAPHY -- GAS CHROMATOGRAPHY MASS SPECTROMETRY
Аннотация: The reaction of a technical mixture of polychlorinated biphenyls with ethanol and potassium hydroxide in dimethyl sulfoxide was studied. The composition of the products formed in the process was determined by gas chromatography and gas chromatography mass spectrometry.

\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2006, v. 79, N. 5, p. 791.pdf
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9.
Инвентарный номер: нет.
   
   R 30


   
    Reactions of epoxides derived from internal perfluoroolefins with o-phenylenediamine and 2-aminophenol [Electronic resource] / L. V. Saloutina, A. Ya. Zapevalov, V. I. Saloutin, M. I. Kodess, V. E. Kirichenko, M. G. Pervova, O. N. Chupakhin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2006. - Vol. 42, № 4. - P558-566
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of epoxy derivatives of internal perfluoroolefins with o-phenylenediamine and 2-aminophenol in dioxane gave 23–67% of the corresponding 2,3-bis(perfluoroalkyl)quinoxalines and 2,3-bis(perfluoroalkyl)-2H-1,4-benzoxazin-2-ols, respectively. When N,N-dimethylacetamide was used as a solvent, the main reaction pathway was anionic isomerization of epoxides into ketones which were then converted into 2-perfluoroalkylbenzimidazoles (in the reactions with o-phenylenediamine) or 2-hydroxy-N-perfluoroalkanoylanilines (in the reactions with 2-aminophenol). The reaction of 3,4-epoxydodecafluorohexane with 2-aminophenol in N,N-dimethylacetamide was accompanied by unusual cyclization to afford 2-pentafluoropropanoyl-2-pentafluoroethyl-1,3-benzoxazolidine

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2006, 42 (4), 558.pdf
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10.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and GC-MS study of fluorinated esters derived from thrimethylolpropane [Electronic resource] / M. G. Pervova, V. E. Kirichenko, T. I. Gorbunova, A. Ya. Zapevalov, V. I. Saloutin // Russian Journal of General Chemistry. - 2008. - Vol. 78, № 9. - P1701-1706
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Zol-gel process was used to synthesize equilibrium mixtures of mono-, di-, and trimester derived from trimethylolpropane and perfluorocarboxylic acids. The elution order of the components of the mixtures from a weakly polar HP-5 column was established. The mass spectra of the synthesized compounds were studied. The GC-MS parameters of the products were compared with the respective parameters of their nonfluorinated analogs. The characteristics of the fluorinated esters have features determined by the esterification degree and the nature of the perfluoroalkyl groups, due to which these compounds can be identified in mixtures

\\\\Expert2\\nbo\\Russian Journal of General Chemistry\\2008, V. 78, N 9, p.1701.pdf
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