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 1-10    11-20   21-30   31-36 
1.
Инвентарный номер: нет.
   
   C 73


   
    Conformational structure of esters of fluorinated acylpyruvic acids [Electronic resource] / P. N. Kondrat'ev, Z. E. Skryabina, V. I. Saloutin, M. N. Rudaya, T. A. Sinitsyna, K. I. Pashkevich // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1990. - Vol. 39, N 6. - P1273-1277
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Esters of fluorinated acylpyruvic acids were obtined for the first time. PMR and IR spectroscopy, dipole moment measurements, and quantum chemical calculations showed that these compounds exist as equilibrium mixtures of E and Z enolic isomers

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1990, 39 (6), 1273.pdf
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2.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and the reactions of trifluoromethylated 1,2,3-triketones 2-(het)arylhydrazones and 4,7-dihydroazolo[5,1-c]triazines [Electronic resource] / O. G. Khudina, E. V. Shchegol'kov, Ya. V. Burgart, M. I. Kodess, O. N. Kazheva, A. N. Chekhlov, G. V. Shilov, O. A. Dyachenko, V. I. Saloutin, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2005. - Vol. 126, № 8. - P1230-1238
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The coupling of trifluoromethylated 1,3-diketones with (het)aryldiazonium chlorides results mainly in the formation of 1,2,3-triketones 2-(het)arylhydrazones while using hetarylamine with a NH-group at the ?-position of the heterocycle as the diazonium component gives 4,7-dihydroazolo[5,1-c]triazines due to cyclization at the trifluoroacetyl fragment. Trifluoromethylated 1,2,3-triketones 2-(het)arylhydrazones and 7-hydroxy-4,7-dihydroazolo[5,1-c]triazines react regio-selectively with methyl hydrazine and phenyl hydrazine to form 3-CF3-pyrazoles. The long-range coupling constants (JF-H) of 1-methylpyrazoles and the chemical shifts of trifluoromethyl groups in the 19F NMR spectra can be used for the determination of regio-isomeric structures of mono(trifluoromethyl)-substituted pyrazoles. 2-(Het)arylhydrazones and 4,7-dihydroazolo[5,1-c]triazines with two trifluoromethyl substituents afford the mixtures of cis- and trans-azopyrazoles in the reactions with hydrazines.

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2005, v.126, p.1230.pdf
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3.
Инвентарный номер: нет.
   
   P 80


   
    Polyfluoroalkylated 1,3-thiazolines: synthesis from polyfluoro-2,3-epoxyalkanes [Text] / L. V. Saloutina, A. Ya. Zapevalov, M. I. Kodess, V. I. Saloutin, G. G. Aleksandrov, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2000. - Vol. 104, № 2. - P155-165
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of polyfluoro-2,3-epoxyalkanes with thiourea and thiosemicarbazide results in 2-amino-5-fluoro-4-hydroxy-4,5-di(polyfluoroalkyl)-1,3-thiazolines and 5-fluoro-2-hydrazino-4-hydroxy-4,5-di(polyfluoroalkyl)-1,3-thiazolines, respectively. Asymmetric oxiranes yield mixtures of regioisomers, and the ring opening has been found to occur mainly near the bulkier fluoroalkyl group. The reaction with thiourea proceeds stereospecifically in dimethyl sulfoxide. The molecular structure of E-isomers of 2-amino-5-fluoro-4-hydroxy-4,5-bis(trifluoromethyl)-1,3-thiazoline and 2-amino-5-fluoro-5-heptafluoropropyl-4-hydroxy-4-trifluoromethyl-1,3-thiazoline has been established by X-ray crystallography.????

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4.
Инвентарный номер: нет.
   
   C 52


    Chizhov, D. L.
    Reaction of trifluoromethylated beta-alkoxyenones with tris(trimethylsilyl) phosphite: A temperature influence on regioselectivity [Text] / D. L. Chizhov, G. -V. Roeschenthaler // Journal of Fluorine Chemistry. - 2006. - Vol. 127, № 2. - P235-239
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of tris(trimethylsilyl) phosphite (TMSO)3P and E-trifluoromethyl-alkoxyenones CF3C(O)CHCHOEt and CF3C(O)CHC(OMe)Me yielded mixtures of E-1,2- and Z-1,4-adducts, CF3C(OTMS)[P(O)(OTMS)2]CCH(OAlk)R 2 and CF3(OTMS)CCHCR(OAlk)[P(O)(OTMS)2] 3 where R and Alk = H and Me, or both Me. Conversion of these 1,2-adducts to 1,4-isomers was effected by increased temperature or by exposure to more tris(trimethylsilyl) phosphite. Acid hydrolysis of 2b (R and Alk = Me) gave ketophosphonic acid CF3C(OH)[P(O)(OH)2]CH2COMe in 88% yield, whereas hydrolysis of 2a (R = H and Alk = Et) with KOH in methanol gave CF3C(OH)[P(O)(OK)2]CHCHOEt in 37% yield. Acid hydrolysis of 3a (R = H and Alk = Et) and 3b (R and Alk = Me) gave phosphonic acid CF3C(OH)2CHCHP(O)(OH)2 in 82% yield and trifluoromethylated 1,2,5,4-oxaphosphol-3-en

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2006, v.127, p.235.pdf
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5.
Инвентарный номер: нет.
   
   S 73


    Sosnovskikh, V. Ya.
    Structural revision in the reactions of 3-cyanochromones with primary aromatic amines. Improved synthesis of 2-amino-3-(aryliminomethyl)chromones [Text] / V. Ya. Sosnovskikh, V. S. Moshkin, M. I. Kodess // Tetrahedron Letters. - 2009. - Vol. 50, № 47. - P6515-6518
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 3-Cyanochromones react with primary aromatic amines to give 2-amino-3-(aryliminomethyl)chromones as the sole products or as their mixtures with Z- and E-3-anilino-2-salicyloylacrylonitriles, depending on the reaction conditions. With aliphatic amines, 2-amino-3-(alkyliminomethyl)chromones are obtained in good yields. The reaction of 3-cyanochromone with o-phenylenediamine is reinvestigated and proof for the product structure and a possible reaction pathway are presented

\\\\Expert2\\nbo\\Tetrahedron Letters\\2009, v. 50, p.6515.pdf
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6.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of fluorine containing glycolurils and oxazolines from oxides of internal perfluoroolefins [Text] / L. V. Saloutina, A. Ya. Zapevalov, V. I. Saloutin, P. A. Slepukhin, M. I. Kodess, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2009. - Vol. 130, № 10. - P853-860
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
OXIDES OF INTERNAL PERFLUOROOLEFINS -- 1,5-bIS(PERFLUOROALKYL)TETRAAZABICYCLO[3.3.0]OCTANE-3,7-D
Аннотация: The reaction of oxides of internal perfluoroolefins 1–3 with urea gave two kinds of novel fluorine containing N-heterocyclic compounds depending on the solvent nature: 1,5-bis(perfluoroalkyl)tetraazabicyclo[3.3.0]octane-3,7-diones 4a–c and 2-amino-5-fluoro-4,5-bis(perfluoroalkyl)-4,5-dihydrooxazol-4-ols 7a–d. Use of polar dimethylsulfoxide, N,N-dimethylacetamide and acetonitrile afforded glycolurils 4a–c in moderate yields. In dioxane, unexpected cyclization occurred resulting in oxazolines 7a–d in high yields. A similar reaction of oxiranes 2, 3 with urea in aqueous dioxane gave mixtures of 4,5-dihydroxy-4,5-bis(perfluoroalkyl)imidazolidine-2-ones 9b, c, glycolurils 4b, c and oxazolines 7b–d. The molecular structure of trans-isomers of oxazoline 7b and imidazolidine 9b has been established by X-ray crystallography??

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2009, V. 130, P. 853.pdf
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7.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and structure of 2-ethoxy- and 2-aminomethylidene-3-fluoroalkyl-3-oxopropionates [Electronic resource] / M. V. Pryadeina, Ya. V. Burgart, V. I. Saloutin, P. A. Slepukhin, O. N. Chupakhin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2007. - Vol. 43, № 7. - P945-955
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Condensation of ethyl 3-polyfluoroalkyl-3-oxopropionates with excess triethyl orthoformate gave ethyl 3-polyfluoroalkyl-2-ethoxymethylidene-3-oxopropionates which reacted with primary aliphatic, aromatic, and heterocyclic amines to form ethyl 2-alkyl(aryl, hetaryl)aminomethylidene-3-polyfluoroalkyl-3-oxopropionates. According to the X-ray diffraction and IR data, the latter exist in the crystalline state as the corresponding E isomers, while in solution (NMR data), as mixtures of Z and E isomers. Condensation of ethyl 2-ethoxymethylidene-3-oxopropionates with secondary heterocyclic amines (morpholine and pyrrolidine) led to the formation of 2-morpholino(pyrrolidin-1-yl)methylidene-3-fluoroalkyl-3-oxopropionates which were shown to exist as Z isomers both in the crystalline state and in solution

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2007, 43 (7), 945-955.pdf
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8.
Инвентарный номер: нет.
   
   R 30


   
    Steric structure of alkyl 2-aryl(hetaryl)hydrazono-3-fluoroalkyl-3-oxopropionates [Electronic resource] / E. V. Shchegol'kov, Ya. V. Burgart, O. G. Khudina, V. I. Saloutin, O. N. Kazheva, A. N. Chekhlov // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2009. - Vol. 45, № 6. - P801-809
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Steric structure of fluorinated 2-arylhydrazono-3-oxo esters was studied by 1H, 19F, and 13C NMR spectroscopy and X-ray analysis. It was found that these compounds in the crystalline state and in solutions in acetone-d 6, DMSO-d 6, and CDCl3 exist as Z isomers with the ester fragment involved in intramolecular hydrogen bond with the hydrazone NH proton. Exceptions are alkyl 2-arylhydrazono-4,4-difluoro-3-oxobutanoates which exist in acetone-d 6 as mixtures of Z and E isomers, the former prevailing. Unlike fluorinated analogs, ethyl 2-(4-methylphenyl)hydrazono-3-oxobutanoate in crystal has the structure of E isomer in which intramolecular hydrogen bond is formed between the NH proton and acetyl carbonyl group. The same compound in acetone-d 6, DMSO-d 6, and CDCl3 gives rise to a mixture of Z and E isomers, the latter prevailing

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2009, 45 (6), 801.pdf
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9.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of N-[(3-Amino-1,2-dicarba-closo-dodecaboran-1-yl)acetyl] Derivatives of alfa-Amino Acids [Text] / G. L. Levit, V. P. Krasnov, D. A. Gruzdev, A. M. Demin, I. V. Bazhov, O. N. Chupakhin, V. N. Charushin // Collection of Czechoslovak Chemical Communications. - 2007. - Vol. 72, № 12. - P1697-1706
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The N-[(3-amino-1,2-dicarba-closo-dodecaboran-1-yl)acetyl] derivatives of amino acids were prepared starting from N-protected (Ac, Form, Bz, and Boc) 3-amino-1-(carboxymethyl)-o-carboranes and alkyl esters of natural amino acids using the carbodiimide method of coupling and removing the ester groups. All the amides obtained were diastereoisomeric mixtures. Some diastereoisomers were separated and the assignment of the absolute configuration of aminocarborane fragments was performed by X-ray crystallography

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10.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of polyfluoroalkylated 1,4-diazinols and 1,4-oxazinols using polyfluoro-2,3-epoxyalkanes 32 + 13 [Text] / L. V. Saloutina, A. Ya. Zapevalov, M. I. Kodess, V. I. Saloutin // Journal of Fluorine Chemistry. - 1998. - Vol. 87, № 1. - P49-55. - Bibliogr. : p. 55 (13 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
2-AMINOETHANOL -- ETHYLENEDIAMINE -- POLYFLUORO-2,3-EPOXYALKANES -- POLYFLUOROALKYLATED 1,4-DIAZINOLS -- POLYFLUOROALKYLATED 1,4-OXAZINOLS
Аннотация: It has been found that the reactions of polyfluoro-2,3-epoxyalkanes with ethylenediamine and 2-aminoethanol yield 2,3-di(polyfluoroalkyl)-1,5,6-trihydro-1,4-diazin-2-ols and 2,3-di(polyfluoroalkyl)-5,6-dihydro-1,4-oxazin-2-ols, respectively. In the case of unsymmetrical oxiranes mixtures of regioisomeric heterocyclic compounds have been obtained. These reactions were found to give some byproducts - N,N?-bis(polyfluoroacyl)ethylenediamines and N-polyfluoroacyl-2-aminoethanols.

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