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1.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Nesterov D. V., Rodionova A. P., Mekhaev A. V., Patrina A. N., Koryakova O. V., Zhilina E. F., Pestov A. V.
Заглавие : Development of the method of polystyrene chloromethylation using the synthesis in gel approach
Место публикации : Russian chemical bulletin. - 2021. - Vol. 70, № 6. - С. 1149-1153
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): polystyrene--chloromethylation--synthesis in gel
Аннотация: A new method for the preparation of poly(chloromethylstyrene) by synthesis in a gel via treating of linear polystyrene with cyclic formals in thionyl chloride has been developed. The method allows to obtain a polymer with a high degree of functionalization. The degree of chloromethylation depends on the molar ratio of the reagents and the catalyst used. The reactivity of the formals increases in the series 1,3-dioxolane trioxane paraform. The composition and structure of polymer products were characterized by elemental analysis, FTIR spectroscopy, and thermogravimetry. It is established that carrying out of chloromethylation in gel allows, in comparison with the known methods, to achieve a greater degree of functionalization faster and with lower consumption of reagents and solvents.
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2.

Вид документа : Статья из журнала
Шифр издания : Г/S 98
Автор(ы) : Bakhteeva I. A., Medvedeva I. V., Byzov I. V., Konev A. S., Zhakov S. V., Uimin M. A., Demin A. M., Murzakaev A. M., Medvedeva O. M.
Заглавие : Synthesis of Fe@C nanoparticles containing sulfo groups on their surfaces and study of their aggregation behavior in aqueous media
Место публикации : Russian chemical bulletin. - 2021. - Vol. 70, № 4. - С. 722-731
ББК : Г
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): magnetic nanoparticles--iron-carbon--benzenesulfonic acid--ir spectroscopy
Аннотация: Magnetic iron nanoparticles (MNPs) encapsulated in a carbon shells and containing sulfo groups on the surface (Fe@C-SO3H) were synthesized. The aggregative stability of aqueous suspensions of the Fe@C-SO3H nanoparticles was studied in solutions of bovine serum albumin and calcium chloride and in phosphate-buffered saline, which simulate blood plasma. It is shown that the Fe@C-SO3H particles practically do not aggregate in the phosphate buffer saline for a long time (several days). On the contrary, MNPs encapsulated in a protein shells using ultrasonic treatment form aggregates up to 110–120 nm in size under these conditions. Suspensions of the Fe@C-SO3H particles are stable in aqueous solutions of calcium chloride in the range of the solid phase concentration between 0.05 and 0.10 g L−1. The results obtained indicate the possibility of using the functionalized Fe@C-SO3H nanoparticles in vitro experiments in biological media.
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3.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kudyakova Yu.S., Slepukhin P. A., Ganebnykh I. N., Burgart Ya. V., Saloutin V. I., Bazhin D. N.
Заглавие : Functionalized trifluoromethyl-containing lithium β-diketonate in the synthesis of homo- and heteronuclear complexes of rare-earth metals
Место публикации : Russian Journal of Coordination Chemistry. - 2021. - Vol. 47, № 4. - С. 280-295
Ключевые слова (''Своб.индексиров.''): β-diketonates--lanthanides--19f nmr spectroscopy--mass spectrometry
Аннотация: The reactions of functionalized lithium CF3-β-diketonate (LiL) with trivalent rare-earth metal salts in methanol afford homobinuclear and heterobi(tri)nuclear complexes depending on the nature of the transition metal and anion (chlorides, nitrates, and acetates). In the cases of lanthanum(III) and cerium(III), homoleptic complexes [(LnL3)2] are isolated (CIF files CCDC nos. 2031097 (Ia) and 2031102 (Ib)). The reaction of LiL with praseodymium(III) nitrate gives the new trimetallic structure [(LiPrL3)(LiL)(NO3)(H2O)2] (CIF file CCDC no. 2031103 (II)), and the replacement of nitrate by chloride gives [(PrL3)(LiL)(H2O)] (CIF file CCDC no. 2031104 (IIIa)). Regardless of the nature of the anion of the salt in the series from neodymium(III) to ytterbium(III) and yttrium(III), Ln–Li β-diketonates [(LnL3)(LiL)(solv)] (solv is H2O and MeOH) are formed, and their structures are characterized by X-ray structure analysis (CIF files CCDC nos. 2031099 (IIIb), 2031100 (IIIc), 2031098 (IVa), 2031096 (IVc), 2031094 (IVf), 2031101 (IVg), and 2031095 (IVh)). The equilibrium of the diketonate isomeric forms in a solution of deuterated dimethyl sulfoxide is studied by 19F NMR spectroscopy, and the qualitative composition of the polynuclear complexes is determined by mass spectrometry.
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4.

Вид документа : Статья из журнала
Шифр издания : Г/K 46
Автор(ы) : Chulakov E. N., Korolyova M. A., Sadretdinova L. S., Tumashov A. A., Kodess M. I., Levit G. L., Krasnov V. P.
Заглавие : Kinetic resolution of racemic 6-substituted 1,2,3,4-tetrahydroquinaldines with chiral acyl chlorides. Experiment and quantum chemical simulation
Место публикации : Russian chemical bulletin. - 2021. - Vol. 70, № 5. - С. 890-899
ББК : Г
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A comparative study of the kinetic resolution (KR) of racemic 6-substituted 2-methyl-1,2,3,4-tetrahydroquinolines with acyl chlorides of (S)-naproxen, N-phthaloyl-(S)-leucine, and (R)-O-phenyllactic acid was carried out. The selectivity factors in the KR of racemic amines with acyl chlorides of (S)-naproxen and (R)-O-phenyllactic acid were shown to be approximately the same and higher than those for the KR of N-phthaloyl-(S)-leucyl chloride. The reasons for the stereodifferentiation in the KR of racemic tetrahydroquinaldines containing groups of different electronic properties by acyl chlorides of three different chiral acids were explained using the DFT method. The conditions for stabilizing π—π interactions of aromatic fragments of the reagents, which do not occur in the same form in the transition state and lead to the minor diastereoisomeric product, are created in the transition state of the faster acylation reaction with (S)-naproxen and (R)-O-phenyllactic acyl chlorides. In the case of the KR of 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methyl-6-methoxy-1,2,3,4-tetrahydroquinoline with N-phthaloyl-(S)-leucyl chloride, the acylation diastereoselectivity is determined, most likely, by conformational factors. The individual (S)-enantiomer of 2-methyl-6-methoxy-1,2,3,4-tetrahydroquinoline of high optical purity was synthesized using the KR of the racemate with (S)-naproxen acyl chloride.
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5.

Вид документа : Статья из журнала
Шифр издания : Г/I-60
Автор(ы) : Kapitanova E. I., Ibragimova A. A., Petrova Y. S., Pestov A. V., Neudachina L. K.
Заглавие : Influence of the degree of chitosan sulfoethylation on the sorption of palladium(ii) chloride complexes from multicomponent solutions
Место публикации : Russian Journal of Applied Chemistry. - 2018. - Vol. 91, № 2. - С. 297-303
ББК : Г
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
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6.

Вид документа : Статья из журнала
Шифр издания : 54/A 10
Автор(ы) : Irgashev R. A., Kazin N. A., Kim G. A., Rusinov G. L., Charushin V. N.
Заглавие : A new synthetic approach to fused nine-ring systems of the indolo[3,2-b] carbazole family through double Pd-catalyzed intramolecular C-H arylation [Электронный ресурс]
Место публикации : RSC Advances. - 2016. - Vol. 6, № 74. - С. 70106-70116
Систем. требования: http://apps.webofknowledge.com/full
Примечания : 26.10.16
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): ight-emitting-diodes --bipolar host materials--hole-transporting materials
Аннотация: A series of new polycyclic compounds bearing the 5,11-dihydroindolo[3,2-b] carbazole ring system, as the common motif of their nine-ring scaffolds, has been successfully prepared with the usage of an efficient two-step strategy, based on the double Friedel-Crafts acylation of 5,11-dihexyl-6,12-di(hetero) aryl-substituted 5,11-dihydroindolo[3,2-b] carbazoles with 2-iodobenzoyl chloride in the presence of SnCl4, followed by regioselective palladium-catalyzed cyclization of the obtained 2,8-bis(2-iodobenzoyl) derivatives into the desired fused 9H-fluoren-9-ones. Some modifications of these nine-ring structures have been performed to afford compounds of the same family bearing the 9H-fluorene fragments. Basic photophysical and electrochemical properties as well as thermal stability of the new fused indolo[3,2-b] carbazole derivatives have been determined.
\\\\expert2\\NBO\\RSC Advances\\2016. Vol. 6, N 74. P. 70106.pdf
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7.

Вид документа : Статья из журнала
Шифр издания : 54/A 19
Автор(ы) : Vakarov S. A., Gruzdev D.A., Chulakov E.N., Sadretdinova L. Sh., Tumashov A. A., Pervova M. G., Ezhikova M. A., Kodess M. I., Levit G. L., Krasnov V. P., Charushin V. N.
Заглавие : Acylative kinetic resolution of racemic heterocyclic amines with (R)-2-phenoxypropionyl chloride
Место публикации : Tetrahedron: Asymmetry . - 2016. - Vol. 27, № 24. - С. 1231-1237
Примечания : Bibliogr. : p. 1236-1237 (15 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): heterocyclic amines --benzoxazines-- 2-methylindoline--kinetic resolution
Аннотация: The acylative kinetic resolution of racemic heterocyclic amines such as 3,4-dihydro-3-methyl-2H-[1,4]benzoxazines, 3,4-dihydro-3-methyl-2H-[1,4]benzothiazine, 2-methyl-1,2,3,4-tetrahydro-quinolines and 2-methylindoline with enantiopure (R)-2-phenoxypropionyl chloride has been studied. It has been found that acylation of 3,4-dihydro-3-methyl-2H-[1,4]benzothiazine proceeds with the best stereoselectively when compared with other racemic amines. An efficient method for the preparation of (S)-3,4-dihydro-3-methyl-2H-[1,4]benzothiazine (99.4% ee) via a kinetic resolution protocol was developed. The possibility of recycling (R)-2-phenoxypropionic acid has been demonstrated.
\\\\expert2\\NBO\\Tetrahedron Asymmetry\\2016, v. 27, p.1231.pdf
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8.

Вид документа : Статья из журнала
Шифр издания : 54/S 45
Автор(ы) : Beryozkina T., Zhidovinov S., Shafran Yu., Eltsov O. S., Slepukhin P. A.
Заглавие : Self-condensation of β-(isoxazol-5-yl) enamines under treatment with acetyl chloride and acids. Synthesis of novel 1,3-diisoxazolyl-1,3-dieneamines and 1,3,5-triisoxazolyl benzenes [Электронный ресурс]
Место публикации : Tetrahedron. - 2014. - Vol.70, №25. - С. 3915-3923
Систем. требования: http://libgen.org/scimag/get.php?doi=10.1016%2Fj.tet.2014.04.015
Примечания : Bibliogr. : p. . - 13.08.2014
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): 1,3,5-triisoxazolyl benzenes--dieneamines--enamines
Аннотация: Two directions for self-condensation of β-(isoxazol-5-yl) enamines under treatment with either acetyl chloride or acids were found leading to new 1,3-diisoxazolyl-1,3-dieneamines and 1,3,5-triisoxazolyl benzenes. The effect of solvent, acid, temperature and the reaction time on the ratio of reaction products were investigated. Trans-E-cis configuration of prepared 1,3-diisoxazolyl-1,3-dieneamines was unambiguously confirmed by 2D NMR spectra and X-ray analysis. A new mechanism of 1,3-diisoxazolyl-1,3-dieneamines formation was prop
\\\\expert2\\nbo\\Tetrahedron\\2014, v. 70 (25), p. 3915.pdf
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9.

Вид документа : Статья из журнала
Шифр издания : 54/N 10
Автор(ы) : Gruzdev D.A., Vakarov S. A., Levit G. L., Krasnov V. P.
Заглавие : N-Tosyl-(S)-Prolyl Chloride in Kinetic Resolution of Racemic Heterocyclic Amines
Место публикации : Chemistry of Heterocyclic Compounds. - 2014. - Article in Press. - С. 1-13
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): h-[1,4]benzoxazine--acylation--amines
Аннотация: The kinetic resolution of racemic heterocyclic amines via acylation with N-tosyl-(S)-prolyl chloride was systematically investigated. It was established that racemic mixtures of aromatic amines could be resolved with high efficiency, while the acylation of 2- and 3-methylpiperidines occurred with low diastereoselectivity. A method for the preparation of enantiomerically pure (3 R)-7,8-difluoro-3-methyl-3,4-dihydro-2 H-[1,4]benzoxazine was developed
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10.

Вид документа : Статья из журнала
Шифр издания : 54/A 10
Автор(ы) : Shchegol'kov E. V., Ivanova A. E., Burgart Ya. V., Saloutin V. I.
Заглавие : A convenient approach to 4,7-dihydrotetrazolo [5,1-c ][1,2,4]triazine synthesis
Место публикации : Journal of Heterocyclic Chemistry. - 2013. - Vol.50. - С. E80-E86
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): triazine synthesis--1,3-dicarbonyl --isomerism
Аннотация: Azo coupling of 1,3-dicarbonyl compounds with tetrazolyl-5-diazonium chloride is used to develop a convenient one-step procedure for the synthesis of 4,7-dihydrotetrazolo[5,1-c][1,2,4]triazines. In contrast to nonfluorinated analogs, 7-hydroxy-7-polyfluoroalkyl-4,7-dihydrotetrazolo[5,1-c][1,2,4]triazines undergo a ring-chain isomerism resulting from the cleavage at the C7 - N7a bond. A distinctive feature of nonfluorinated 4,7-dihydrotetrazolo[5,1-c][1,2,4] triazines is the possibility to dehydration, which is accompanied by an azide rearrangement due to the tetrazole ring cleavage with the formation of tetrazolo[1,5-b][1,2,4]triazines
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