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 Найдено в других БД:Труды сотрудников Института химии твердого тела УрО РАН (1)Публикации Чарушина В.Н. (22)
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1.
Инвентарный номер: нет.
   
   U 62


   
    Unusual transformations of lithium enolate of ethyl 4,4,4-trifluoro-3-oxobutanoate [Электронный ресурс] / N. S. Boltacheva, P. A. Slepukhin, D. L. Chizhov, D. S. Yachevskii, V. I. Filyakova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2012. - Vol.61, №3. - P563-567
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
LITHIUM -- ENOLATES -- UNUSUAL REACTIONS
Аннотация: The present paper describes unusual reactions of lithium enolate of ethyl 4,4,4-trifluoro-3-oxobutanoate with ammonium acetate and 1-aminonaphthalene. These reactions produce 4-amino-2,6-bis(trifluoromethyl)pyridine and 4-trifluoromethyl-2-[(Z)-1,1,1-trifluoroprop-1-en-2-ol-1-yl]benzo[h]quinoline, respectively. The reaction of 1,1,7,7,7-hexafluoroheptane-2,4,6-trione hydrate with 1-naphthylamine gives a mixture of 4-trifluoromethyl-2-[(Z)-1,1,1-trifluoroprop-1-en-2-ol-1-yl]benzo[h]quinoline and N,N′-bis(naphth-1-yl)-2,6-bis(trifluoromethyl)pyridine-4(1H)-imine, respectively

\\\\Expert2\\NBO\\Russian Chemical Bulletin\\2012, 61 (3), 563-567.pdf
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2.
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    2-Pyridoyltrifluoroacetyl acetone in synthesis of 3d-4f complexes [Co-2(II)Ln-2(III)(L)-8(OH)-2] with dicubane structure / D. L. Chizhov, D. S. Yachevskii, N. S. Boltacheva, V. I. Filyakova, O. N. Chupakhin, V. N. Charushin // The 14-th International Conference of Molecule-based Magnets : absr. book, Saint Petersburg, Russia, July 5-10 2014. - СПб., 2014. - P-622. - С. 123
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
3d-4f COMPLEXES -- 2-PYRIDOYLTRIFLUOROACETYL ACETONE

\\\\expert2\\NBO\\The 14-th International Conference of Molecule-based Magnets\\The 14-th International Conference of Molecule-based Magnets.pdf
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3.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of podands modified with thiosemicarbazide and fluoroalkyl(hydroxy)pyrazoline fragments / V. I. Filyakova, P. A. Slepukhin, N. S. Boltacheva, E. B. Letova, V. N. Charushin // Russian Journal of General Chemistry. - 2017. - Vol. 87, № 5. - P957-962
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PODANDES -- X-RAY DIFFRACTION ANALYSIS -- ACETIC ACID -- ORGANIC ACIDS
Аннотация: 1,8-Bis(diisothiosemicarbazido)-3,6-dioxaoctane have been synthesized by subsequent treatment of 2,2 -(ethylenedioxy)bisethylamine with carbon disulfide, sodium chloroacetate, and hydrazine hydrate. 1,8-Bis- (diisothiosemicarbazido)-3,6-dioxaoctane has reacted with lithium 1,1-difluoropenta-2,4-dionate in glacial acetic acid to yield 1,8-bis[5R*,5 R*(5-hydroxy-5-difluoromethyl-4,5-dihydro-3-methyl-1H-pyrazol-1-yl)-1-carbothioamido]-3,6-dioxaoctane. The molecular and crystal structure of the product has been determined by X-ray diffraction analysis.

\\\\Expert2\\NBO\\Russian Journal of General Chemistry\\2017 V 87 P957.pdf
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4.
Инвентарный номер: нет.
   
   D 44


   
    Deprotonation of pyrazole and its analogs by aqueous copper acetate in the presence of triethylamine / M. A. Yakovleva , E. V. Kushan, N. S. Boltacheva, V. I. Filyakova, S. E. Nefedov // Russian Journal of Inorganic Chemistry (Zhurnal Neorganicheskoi Khimii). - 2012. - Vol. 57, № 2. - С. 181-192
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SECONDARY BUILDING UNITS -- MAGNETIC-PROPERTIES -- COORDINATION POLYMERS
Аннотация: Deprotonation reactions of pyrazole and its analogs by aqueous copper acetate in benzene at room temperature in the presence of triethylamine were studied. Unlike 3,5-dimethylpyrazole, more acidic pyrazole, 5-methyl-3-trifluoromethylpyrazole, and 3,5-bis(trifluoromethyl)pyrazoles are deprotonated to give pyrazolate bridges. The structural features of the obtained compounds are discussed based on X-ray diffraction data

\\\\Expert2\\nbo\\Russian Journal of Inorganic Chemistry\\2012, v. 57, N. 2, p.181-192.pdf
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5.
Инвентарный номер: нет.
   
   F 33


   
    Features of the reaction of 3(5)-methyl-5(3)-trifluoromethylpyrazole with chloroform. Synthesis and structure of fluorinated analogs of tris(pyrazol-1-yl)methane / N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova, M. A. Samorukova, L. G. Lavrenova, V. I. Filyakova, V. N. Charushin // Russian Journal of General Chemistry. - 2012. - Vol.82, №8. - С. 1444-1450
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHLOROFORM -- TRIFLUOROMETHYLPYRAZOLE -- TRIS(PYRAZOL-1-YL)METHANE
Аннотация: Reaction of 3(5)-methyl-5(3)-trifluoromethylpyrazole (I) with chloroform leads to a complex mixture of compounds. The main components are {bis[(5-methyl-3-trifluoromethyl)pyrazol-1-yl](3-methyl-5-trifluoromethyl)pyrazol-1-yl}methane, bis{[(3-methyl-5-trifluoromethyl)pyrazol-1-yl](5-methyl-3-trifluoromethyl)-pyrazol-1-yl}methane, and tris[(3-methyl-5-trifluoro-methyl)pyrazol-1-yl]methane. The structure of isomeric substances was proved by XRD method

\\\\Expert2\\nbo\\Russian Journal of General Chemistry\\2012, V. 82, N 8, p. 1444–1450.pdf
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6.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis, structure and complexation of the fluorinated 1,3-enaminoketones containing at the nitrogen atom substituents with a terminal C≡C bond [Electronic resource] / E. F. Zhilina, P. A. Slepukhin, N. S. Boltacheva, M. G. Pervova, D. L. Chizhov, V. I. Filyakova, V. N. Charushin // Russian Journal of General Chemistry. - 2012. - Vol. 82, №12. - P1962-1969
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SYNTHESIS -- NITROGEN -- TERMINAL C≡C BONDS
Аннотация: The reaction of fluorinated lithium 1,3-diketonates with propargylamine hydrochloride and 1,1,1-trifluorpentane-2,4-dione or 1,1,1-trifluoro-4-methoxypent-3-en-2-one with propargylamine and 3-aminophenylacetylene were performed to obtain fluorinated 1,3-enaminones containing at a nitrogen atom substituents with terminal C≡C bonds: (Z)-1,1,1-trifluoro-4-(2-propynylamino)-3-pentene-2-one, (Z)-1,1,2,2-tetrafluoro-5-(2-propynylamino)-4-hexen-3-one, and 4-(3-ethynylphenylamino)-1,1,1-trifluoropentyl-3-en-2-one. Reactions of 4-(3-ethynyl-phenylamino)-1,1,1-trifluoro-pentyl-3-en-2-one with Cu(II) acetate or nanosized powder of copper or its oxides led to the respective chelate complex. The structure of (Z)-1,1,2,2-tetrafluoro-5-(2-propynylamino)-4-hexen-3-one and a copper complex of 4-(3-etinilphenylamino)-1,1,1-trifluoropenta-3-en-2-one was determined by XRD

\\\\Expert2\\NBO\\Russian Journal of General Chemistry\\2012, V. 82, N 12, p. 1962–1969.pdf
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7.
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    Polyfluoroalkyl-2-hydroxyimino-1,3-diketones as new selective carboxylesterase inhibitors / N. P. Boltneva, S. V. Lushchekina, O. G. Serebryakova [и др.] // MedChem-Russia 2021: материалы 5-ой Российской конференции по медицинской химии с международным участием. - Волгоград, 2021. - С. 256
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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8.
Инвентарный номер: нет.
   


   
    Oximes of fluoroalkyl-containing 1,3-diketones: specific features of synthesis, analysis, and thermal stability / N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova [et al.] // Russian chemical bulletin. - 2022. - Vol. 71, № 7. - P1464-1473
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Nitrosation of lithium 1,3-diketonates bearing fluoroalkyl and aryl (or hetaryl) substituents in positions 1 and 3 results in 3-polyfluoroalkyl-1,2,3-propanetrione 2-oximes (from this point on, oximes). Under similar conditions, lithium (Z)-1,1,1-trifluoro-4-oxo-4-(thien-2-yl)-2-buten-2-olate forms a hydration product of the corresponding oxime. Nitrosation of fluoroalkyl-containing lithium 1,3-diketonates is accompanied by retro-decomposition of the initial lithium 1,3-diketonates and the target oximes (or their hydration products) followed by oxidation and hydrolysis of the reaction products. Under the GC-MS conditions, the oximes undergo partial thermal decomposition to 2-aryl(hetaryl)-2-oxoethanenitriles. An analysis of solutions of the oximes in DMSO-d6 by 1H and 19F NMR spectroscopies revealed isomerization and hydration of these compounds. The temperature ranges of stability of the oximes were determined by thermogravimetric analysis and differential thermal analysis. The molecular and crystal structures of 4,4-difluoro-1-(4-methoxyphenyl)-1,2,3-butanetrione 2-oxime and 4,4,4-trifluoro-1-(thien-2-yl)-1,2,3-butanetrione 2-oxime were determined by X-ray diffraction.

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9.
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    Oximes of fluoroalkyl-containing 1,3-diketones: specific features of synthesis, analysis, and thermal stability / N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova [et al.] // Russian chemical bulletin. - 2022. - Vol. 71, № 4. - P1464-1473
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Nitrosation of lithium 1,3-diketonates bearing fluoroalkyl and aryl (or hetaryl) substituents in positions 1 and 3 results in 3-polyfluoroalkyl-1,2,3-propanetrione 2-oximes (from this point on, oximes). Under similar conditions, lithium (Z)-1,1,1-trifluoro-4-oxo-4-(thien-2-yl)-2-buten-2-olate forms a hydration product of the corresponding oxime. Nitrosation of fluoroalkyl-containing lithium 1,3-diketonates is accompanied by retro-decomposition of the initial lithium 1,3-diketonates and the target oximes (or their hydration products) followed by oxidation and hydrolysis of the reaction products. Under the GC-MS conditions, the oximes undergo partial thermal decomposition to 2-aryl(hetaryl)-2-oxoethanenitriles. An analysis of solutions of the oximes in DMSO-d6 by 1H and 19F NMR spectroscopies revealed isomerization and hydration of these compounds. The temperature ranges of stability of the oximes were determined by thermogravimetric analysis and differential thermal analysis. The molecular and crystal structures of 4,4-difluoro-1-(4-methoxyphenyl)-1,2,3-butanetrione 2-oxime and 4,4,4-trifluoro-1-(thien-2-yl)-1,2,3-butanetrione 2-oxime were determined by X-ray diffraction.

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10.
Инвентарный номер: нет.
   


   
    Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5h)-one oximes / N. V. Palysaeva, A. B. Sheremetev, N. S. Boltacheva, P. A. Slepukhin, M. G. Pervova, V. I. Filyakova, V. N. Charushin // Mendeleev Communications. - 2018. - Vol. 28, № 1. - P126-127
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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