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 Найдено в других БД:Труды сотрудников Института химии твердого тела УрО РАН (1)Публикации Чарушина В.Н. (8)
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1.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Boltacheva N. S., Slepukhin P. A., Pervova M. G., Rudina A. Kh., Chemagina I. V., Taibinov N. P., Filyakova V. I., Loboiko B. G., Charushin V. N.
Заглавие : Oximes of fluoroalkyl-containing 1,3-diketones: specific features of synthesis, analysis, and thermal stability
Место публикации : Russian chemical bulletin. - 2022. - Vol. 71, № 7. - С. 1464-1473
Предметные 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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2.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Elkina N. A., Shchegolkov E. V., Burgart Y. V., Agafonova N. A., Perminova A. N., Saloutin V. I., Gerasimova N. A., Evstigneeva N. P.
Заглавие : Synthesis and biological evaluation of polyfluoroalkyl-containing 4-arylhydrazinylidene-isoxazoles as antifungal agents with antioxidant activity
Место публикации : Journal of Fluorine Chemistry. - 2022. - Vol. 254. - Ст.109935
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
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3.

Вид документа :
Шифр издания :
Автор(ы) : Boltacheva N. S., Slepukhin P. A., Pervova M. G., Rudina A. Kh., Chemagina I. V., Taibinov N. P., Filyakova V. I., Loboiko B. G., Charushin V. N.
Заглавие : Oximes of fluoroalkyl-containing 1,3-diketones: specific features of synthesis, analysis, and thermal stability
Место публикации : Russian chemical bulletin. - 2022. - Vol. 71, № 4. - С. 1464-1473
Предметные 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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4.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kushch S. O., Goryaeva M. V., Burgart Ya. V., Triandafilova G. A., Malysheva O. K., Krasnykh O. P., Gerasimova N. A., Evstigneeva N. P., Saloutin V. I.
Заглавие : Facile synthesis of 6-organyl-4-(trifluoromethyl)pyridin-2(1H)-ones and their polyfluoroalkyl-containing analogs
Место публикации : Russian chemical bulletin. - 2022. - Vol. 71, № 8. - С. 1687-1700
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The three-component cyclization of 3-polyfluoroalkyl-3-oxopropanoates and methyl ketones with ammonium acetate affords 6-organyl-4-(polyfluoroalkyl)pyridin-2(1H)-ones (organyl is alkyl, aryl, or hetaryl). The synthesized pyridones were evaluated for antifungal, antibacterial, and analgesic activity.
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5.

Вид документа : Статья из журнала
Шифр издания : Г/P 58
Автор(ы) : Semenova A. M., Ezhikova M. A., Kodess M. I., Zapevalov A. Y., Pestov A. V.
Заглавие : Phosgene-free synthesis of symmetric bis(polyfluoroalkyl) carbonates
Место публикации : Mendeleev Communications. - 2021. - Vol. 31, № 2. - С. 257-258
ББК : Г
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): transesterification--titanium alkoxides--polyfluoalkanols--dialkyl carbonates--organofluorine compounds
Аннотация: A phosgene-free synthesis of symmetric bis(polyfluoroalkyl) carbonates involves the transesterification of diphenyl carbonate with polyfluoroalkanols promoted by stoichiometric amounts of titanium(iv) alkoxides.
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6.

Вид документа : Статья из журнала
Шифр издания : Г/E 27
Автор(ы) : Kudyakova Y. S., Onoprienko A. Y., Edilova Y. O., Burgart Y. V., Saloutin V. I., Bazhin D. N.
Заглавие : Effect of the nature of a fluorinated substituent on the synthesis of functionalized 1,3-diketones
Место публикации : Russian chemical bulletin. - 2021. - Vol. 70, № 4. - С. 745-752
ББК : Г
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The synthesis of alkali metal and copper(II) 1-polyfluoroalkyl-4,4-dimethoxypentane-1,3-dionates is reported. The subsequent treatment of these compounds with oxalic acid or ethylenediaminetetraacetic acid disodium salt affords functionalized 1,3-diketones. The nature of the polyfluoroalkyl substituent was found to affect the conditions of the Claisen condensation and the stability of the acetal group in acidic medium.
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7.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Agafonova N. A., Burgart Y. V., Gerasimova N. A., Evstigneeva N. P., Saloutin V. I.
Заглавие : Alternative approaches to the synthesis of polyfluoroalkyl-containing 1-methyl-4-nitrosopyrazoles
Место публикации : Russian chemical bulletin. - 2021. - Vol. 70, № 6. - С. 1135–1140
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): 4,4,4-trifl uoro-3,3-dihydroxy-2-(hydroxyimino)butan-1-ones--polyfl uoroalkyl2-hydroxyimino-1,3-diketones--1-methyl-4-nitrosopyrazoles--mycostatic activity
Аннотация: We studied different approaches to the synthesis of polyfluoroalkyl-containing 1-methyl-4-nitrosopyrazoles, which are based on the cyclization of 4,4,4-trifluoro-3,3-dihydroxy-2-hydroxyimino-1-R-butan-1-ones or 2-hydroxyimino-1,3-diketones with methylhydrazine and on a one-pot sequential treatment of 1,3-diketones with sodium nitrite and methylhydrazine. It was found that the regioselectivity of the formation of 1-methyl-4-nitrosopyrazoles is affected by the steric factors of 1,3-dicarbonyl reagents. The study of the mycostatic effect of 4-nitrosopyrazoles showed that the introduction of a bulky polyfluoroalkyl or tert-butyl substituent leads to a decrease in their activity.
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8.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kushch S. O., Goryaeva M. V., Surnina E. A., Burgart Y. V., Ezhikova M. A., Kodess M. I., Slepukhin P. A., Saloutin V. I.
Заглавие : Multicomponent domino reactions for the synthesis of variable hydrogenated imidazo[1,2-a]pyridines
Место публикации : Asian journal of organic chemistry. - 2021. - № 11. - С. e2021007
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Autocatalyzed one-pot multicomponent cyclization of polyfluoroalkyl-3-oxo ester and ethylenediamine with aldehyde is an effective approach to octa-, hexa- and tetrahydroimidazo[1,2-a]pyridines generated mainly due to the α,β-unsaturated aldehyde addition, often formed in situ, to the 3-oxo ester methylene fragment, followed by the pyridine backbone closure at one of the carbonyl groups.
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9.

Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Boltneva N. P., Lushchekina S. V., Serebryakova O. G., Rudakova E. V., Astakhova T.Yu., Agafonova N. A., Shchegolkov E. V., Boltacheva N. S., Filyakova V. I., Radchenko E. V., Palyulin V. A., Makhaeva G. F., Burgart Ya. V., Saloutin V. I., Richardson R. J.
Заглавие : Polyfluoroalkyl-2-hydroxyimino-1,3-diketones as new selective carboxylesterase inhibitors
Место публикации : MedChem-Russia 2021: материалы 5-ой Российской конференции по медицинской химии с международным участием. - Волгоград, 2021. - С. 256
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Shchegolkov E. V., Burgart Y. V., Matsneva D. A., Saloutin V. I., Borisevich S., Kadyrova R. A., Orshanskaya I. R., Zarubaev V. V.
Заглавие : Polyfluoroalkylated antipyrines in Pd-catalyzed transformations
Место публикации : RSC Advances. - 2021. - Vol. 11, № 56. - С. 35174-35181
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: In the direct C–H arylation with arylhalogenides in the presence of Pd(OAc)2, trifluoromethyl-containing antipyrine reacts very slowly and incompletely owing to the low nucleophilicity of its C4 center. However, it was effective in modifying polyfluoroalkyl-substituted 4-bromo- and 4-iodo antipyrines by the Suzuki and Sonogashira reactions. It was established that using Pd2(dba)3 as catalyst and XPhos as phosphine ligand was the optimal catalytic system for the synthesis of 4-aryl- and 4-phenylethynyl-3-polyfluoroalkyl-antipyrines. Moreover, iodo-derivatives as the initial reagents were found to be more advantageous compared to bromo-containing analogs. It was found that 4-phenylethynyl-5-CF3-antipyrine has a moderate activity against the influenza virus A/Puerto Rico/8/34 (H1N1) and 4-iodo-5-CF3-antipyrine reveals a weak activity against the vaccine virus (strain Copenhagen) and bovine diarrhea virus (strain VC-1).
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