Главная Новые поступления Описание Шлюз Z39.50

Базы данных


Труды сотрудников Института органического синтеза УрО РАН - результаты поиска

Вид поиска

Область поиска
в найденном
 Найдено в других БД:Каталог книг и продолжающихся изданий (1)Труды сотрудников Института теплофизики УрО РАН (6)Труды сотрудников Института химии твердого тела УрО РАН (3)Публикации Черешнева В.А. (2)Публикации Чарушина В.Н. (15)
Формат представления найденных документов:
полный информационныйкраткий
Отсортировать найденные документы по:
авторузаглавиюгоду изданиятипу документа
Поисковый запрос: (<.>K=DERIVATIVE<.>)
Общее количество найденных документов : 56
Показаны документы с 1 по 20
 1-20    21-40   41-56 
1.

Вид документа : Статья из журнала
Шифр издания : 54/Z 99
Автор(ы) : Chupakhin O. N., Kozhevnikov V. N., Kozhevnikov D. N., Rusinov V. L.
Заглавие : [1,5]Sigmatropic shift of hydrogen in amination of 3-pyrrolidino-1,2,4- triazine 4-oxide
Место публикации : Tetrahedron Letters. - 1999. - Vol. 40, № 33. - С. 6099-6100
Примечания : Bibliogr. : p. 6100 (11 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reaction of 3-pyrrolidino-1,2,4-triazine 4-oxide with ammonia leads to the product of tele-substitution of pyrrolidine - 5-amino-1,2,4-triazine 4-oxide. Sigmatropic shift of hydrogen postulated for such reactions has been proved by isolation of key intermediates.
Найти похожие

2.

Вид документа : Статья из журнала
Шифр издания : 54/V 29
Автор(ы) : Varaksin M. V., Utepova I. A., Chupakhin O. N.
Заглавие : Direct C-C coupling of cyclic aldonitrones with 1,2,4-triazines using SN H reactions
Место публикации : Chemistry of Heterocyclic Compounds. - 2012. - Vol.48, №8. - С. 1213-1219
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): 1,2,4-triazines-- aldonitrones--snh reactions
Аннотация: New nitrogen heterocyclic derivatives were obtained by a direct uncatalyzed by metals C-C cross-coupling of a cyclic aldonitrone lithium derivative with 1,2,4-triazines
\\\\Expert2\\NBO\\Chemistry of Heterocyclic Compounds\\2012, v.48, N 8, p.1213-1219.pdf
Найти похожие

3.

Вид документа : Статья из журнала
Шифр издания : 54/U 62
Автор(ы) : Krasnykh O. P., Karpenko N. S., Filyakova V. I., Charushin V. N.
Заглавие : Unusual transformation of a fluoroalkyl-containing beta-aminovinyl ketone [Electronic resource]
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 6. - С. 1355-1356: ил.
Систем. требования: http://www.springerlink.com/content/u726r2722240qq02/fulltext.pdf
Примечания : Библиогр.: с. 1356 (3 ref.). - 3.11.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (6), 1355.pdf
Найти похожие

4.

Вид документа : Статья из журнала
Шифр издания : 54/T 82
Автор(ы) : Azev Y. A., Guselnikova O. L., Chupakhin O. N.
Заглавие : Transformations of 5-diazo derivatives of 1,3-dimethyl-6-hydrazinouracil - new synthetic approaches to novel pyrimidine-derivatives [Electronic resource]
Место публикации : Mendeleev Communications. - 1994. - N 6. - С. 208-209
Систем. требования: http://www.sciencedirect.com/science/article/pii/S0959943694716643
Примечания : 10.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 1,3-Dimethyl-6-hydrazinouracil 1 gives hydrazones 2 with the corresponding aldehydes. Heating of 6-hydrazinouracil 1 in ethanol in the presence of hyrochloric acid results in the formation of N1, N2-bis(1,3-dimethyl-2,6-dioxopyrimid-4-yl)hydrazine 3, which gives the diazo derivative 4 on treatment with 2,4-diazido-6-cyanomethoxy-s-triazine in DMSO in the presence of triethylamine et room temperature
Найти похожие

5.

Вид документа : Статья из журнала
Шифр издания : 54/T 44
Автор(ы) : Chupakhin O. N., Rusinov G. L., Itsikson N. A., Beresnev D. G., Nikolaeva I. L., Burilov A. R., Konovalov A. I.
Заглавие : The first case of direct coupling of heterocycles with calixarenes. Reaction of resorcinarenes with 1,2,4-triazin-5(2H)-ones
Место публикации : Heterocyclic Communications. - 2004. - Vol. 10, № 1. - С. 15-18: ил.
Примечания : Библиогр.: с. 18 (8 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A convenient method for an one-step coupling of resorcinarenes with 3-R-1,2,4-triazin-5(2H)-ones, involving nucleophilic addition to the unsubstituted carbon atom C-6 of triazine ring, has been worked out.
Найти похожие

6.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Filyakova V. I., Kodess M. I., Zapevalov A. Ya., Saloutin V. I.
Заглавие : Synthesis of perfluoro- and 2-trifluoromethylpentafluoro-dihydrofurans and their epoxy derivatives [Electronic resource]
Место публикации : Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2003. - Vol. 39, № 7. - С. 1010-1015
Систем. требования: http://www.springerlink.com/content/tk65261645q64317/fulltext.pdf
Примечания : Bibliogr. : p. 1015 (11 ref.). - 31.10.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Perfluorotetrahydrofuran-2-carboxylic acid was converted through a series of transformations into perfluoro-2,3-dihydrofuran and perfluoro-2,5- dihydrofuran; likewise, from (2-perfluorotetrahydrofuryl)difluoroacetic acid 2-trifluoromethylpentafluoro-2,3-dihydrofuran was obtained. Perfluoro-2,3- dihydrofuran and 2-trifluoromethylpentafluoro-2,3-dihydrofuran underwent isomerization into perfluoro-2,5-dihydrofuran and 2-trifluoromethylpentafluoro- 2,5-dihydrofuran by the action of cesium fluoride. Treatment of perfluoro-2,5-dihydrofuran with SbF5 resulted in ring opening and formation of cis-perfluoro-2-butenoyl fluoride, while 2- trifluoromethylpentafluoro-2,3-dihydrofuran was converted into 2-trifluoromethylpentafluoro-2,5-dihydrofuran under the same conditions. Perfluoro-3,4-epoxytetrahydrofuran and 2-trifluoromethyl-3,4-epoxypenta- fluorotetrahydrofuran containing fused oxirane and tetrahydrofuran rings were synthesized by reactions of perfluoro-2,5-dihydrofuran and 2- trifluoromethylpentafluoro-2,5-dihydrofuran, respectively, with sodium hypochlorite.
\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2003, 39 (7), 1010.pdf
Найти похожие

7.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Varaksin M. V., Tretyakov E. V., Utepova I. A., Romanenko G. V., Bogomyakov A. S., Stass D. V., Sagdeev R.S., Ovcharenko V., Chupakhin O. N.
Заглавие : Synthesis of nitroxyl radical by direct nucleophilic functionalization of a C-H bond in the azadiene systems
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2012. - Vol.61, №7. - С. 1469-1473
Примечания : Bibliogr. : p. 1473 (15 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): nitrones--nitronyl nitroxyls--esr spectra
Аннотация: Cyclic dinitrones underwent nucleophilic substitution of the hydrogen atom in the reaction with a paramagnetic carbanion, the lithium derivative of 4,4,5,5 tetramethyl 4,5 dihydro 1H imidazol 1 oxyl 3 oxide, to give polyfunctional nitronyl nitroxyls
\\\\expert2\\NBO\\Russian Chemical Bulletin\\2012, 61 (7), 1469-1473.pdf
Найти похожие

8.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Musikhina A. A, Utepova I. A., Serebryakov N.S., Chupakhin O. N., Charushin V. N.
Заглавие : Synthesis of chiral ferrocenylazines. Negishi cross-coupling or S N H reactions?
Место публикации : Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2013. - Vol.49, №8. - С. 1191-1194
Примечания : Bibliogr. : p. 1194 (28 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): synthesis--chiral ferrocenylazines--negishi
Аннотация: Preparation of new hetaryl-containing planar chiral ferrocene by a nucleophilic substitution of hydrogen in azines was performed using a lithium derivative of (S)-ferrocenyl-p-tolylsulfoxide as s nucleophilic reagent
\\\\expert2\\NBO\\Russian Journal of Organic Chemistry\\2013, 49, (8), 1191-1194.pdf
Найти похожие

9.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Nosova E. V., Lipunova G. N., Slepukhin P. A., Charushin V. N.
Заглавие : Synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones
Место публикации : Journal of Fluorine Chemistry. - 2013. - Vol.145. - С. 63-65
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): synthesis--nucleophilic substitution--x-ray analysis
Аннотация: A versatile pathway for the synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones from 4,5-difluoroanthranylic acid has been advanced. Nucleophilic amination–defluorination reaction of the 6,7-difluoro derivative of 3-amino-2-methyl-3H-quinazolin-4-one has been established to occur at position 7, as shown by X-ray crystallographic analysis. --------------------------------------------------------------------------------
\\\\Expert2\\NBO\\Journal of Fluorine Chemistry\\2013, v. 145, p.63.pdf
Найти похожие

10.

Вид документа :
Шифр издания : 54/S 98
Автор(ы) : Nosova E. V., Lipunova G. N., Slepukhin P. A., Charushin V. N.
Заглавие : Synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones
Место публикации : Journal of Fluorine Chemistry. - 2012. - С. in Press online 17 October
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): fluorine-containing quinazolinones--3-aminoquinazolin-4-ones--nucleophilic displacement reactions
Аннотация: A versatile pathway for the synthesis of 7-cycloalkylimino substituted 3-amino-6-fluoro-2-methyl-3H-quinazolin-4-ones from 4,5-difluoroanthranylic acid has been advanced. Nucleophilic amination–defluorination reaction of the 6,7-difluoro derivative of 3-amino-2-methyl-3H-quinazolin-4-one has been established to occur at position 7, as shown by X-ray crystallographic analysis
\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2012, Article in Press, 17 October.pdf
Найти похожие

11.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Rudenko D. A., Slepukhin P. A., Karmanov V. I., Vakhrin M. I., Shurov S. N., Shchurov Yu. A.
Заглавие : Synthesis of 5-substituted 8,8-dimethyl-8,9-dihydro-3H,7H-[1,2]oxazino[5,4,3-de]quinolin-3-ones
Место публикации : Chemistry of Heterocyclic Compounds. - 2013. - Vol.48, №10. - 1539-1544
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): hydroxylamine--quantum-chemical calculations--tetrahydroquinoline-4-carboxylic acids
Аннотация: The reaction of 2-substituted 7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids with hydroxylamine results in the formation of 5-substituted 8,8-dimethyl-8,9-dihydro-3H,7H-[1,2]ox-azino[5,4,3-de]quinolin-3-ones. The structure of the 5-phenyl derivative has been established by X-ray structural analysis. A possible mechanism of the reaction has been proposed on the basis of nonempirical quantum-chemical calculations
\\\\Expert2\\NBO\\Chemistry of Heterocyclic Compounds\\2013, v.48, N 10, p. 1539-1544.pdf
Найти похожие

12.

Вид документа :
Шифр издания : 54/S 98
Автор(ы) : Kravchenko M. A., Nosova E. V., Lipunova G. N., Chasovskikh O. M., Sokolov V. A., Charushin V. N.
Заглавие : Synthesis and tuberculostatic activity of fluoridized 3-Z-hydrazine-2-benzoyl acrylates and their cyclization products
Место публикации : Problemy tuberkuleza . - 2003. - №7. - С. 49-52
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): acrylic acid derivative--pyrazole --tuberculostatic agent
Аннотация: A rapid development of the resistance of drugs and their toxic and adverse reactions suggest that new antituberculous drugs should be designed. Of the greatest importance is isoniazid resistance. Testing new compounds (IIa, b) has established that the minimum inhibitory concentration of the drug (IIa), 0.39 microgram/ml suppresses the growth of Mycobacterium tuberculosis (MBT) in the macrophages up to 50%, that of the drug (IIb), 1.56 micrograms/ml, causes death in 25% of cases, which is indicative of the high activity of compounds (IIa, b) against MBT
Найти похожие

13.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Bratskaya S.YU., Azarova Yu. A., Portnyagin A. S., Mechaev A., Voit A., Pestov A. V.
Заглавие : Synthesis and properties of isomeric pyridyl-containing chitosan derivatives
Место публикации : International Journal of Biological Macromolecules . - 2013. - С. 426-432
Примечания : Bibliogr. : p. 431-432 (49 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): chitosan--physical-chemical properties--pyridyl derivative
Аннотация: Here we report on the method of synthesis in gel of a new heterocyclic aminopolymer-N-2-(4-pyridyl)ethylchitosan (4-PEC) via direct addition of 4-vinylpyridine to chitosan that yields a derivative with the substitution degree (DS) up to 0.8. The comparison of reactivity, thermal, spectroscopic, and sorption properties of a new derivative and its isomer N-2-(2-pyridyl)ethylchitosan (2-PEC) is presented. 2-PEC has higher sorption capacity and forms more stable chelates with [PdCl4]2- and [PtCl6]2- ions than 4-PEC, but the latter shows higher selectivity to noble metals ions in the presence of Cl- ions. A gradual increase of the sorption capacities and the affinity coefficient for Cu2+ and Ni2+ in the row chitosan4-PEC2-PEC was related to the increase of electron donor nitrogen atoms content and chelating properties of 2-PEC. A nearly negligible increase of the 4-PEC sorption capacity for Ag+, as compared to plain chitosan, was suggested to be dependent on the difference in complexation models for 2-PEC and 4-PEC derivatives. The density functional theory (DFT) calculations have shown that the "pendant" model of the complex with Ag(I) is energetically favorable only for 2-PEC derivative, while in cases of chitosan and 4-PEC only "bridge" complexes can be formed that results in lower sorption capacity
Найти похожие

14.

Вид документа : Статья из журнала
Шифр издания : 54/S 98
Автор(ы) : Nosova E. V., Stupina T. V., Lipunova G. N., Charushin V. N.
Заглавие : Synthesis and fluorescent properties of 2-styryl-6,7-difluoro-8-hydroxyquinoline and its Zn(II) complex
Место публикации : Journal of Fluorine Chemistry. - 2013. - Vol.150. - С. 36-38
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): styrylquinoline--zn(ii) complex--fluorinated quinolines
Аннотация: A synthetic approach to 2-methyl-6,7-difluoro-8-hydroxyquinoline, a key intermediate, has been developed. 6,7-Difluoro derivative of 2-styryl substituted 8-hydroxyquinoline and its Zn(II) complex have been obtained. Effects of fluorine atoms in the benzene ring on photophysical properties of 2-styryl-8-hydroxyquinolines and their Zn(II) complexes have been studied
\\\\Expert2\\NBO\\Journal of Fluorine Chemistry\\2013, v. 150, p.36.pdf
Найти похожие

15.

Вид документа :
Шифр издания : 54/S 89
Автор(ы) : Bazhin D. N., Schegolkov E. V., Kudyakova Yu.S., Burgart Ya. V., Saloutin V. I.
Заглавие : Structure of diethyl (polyfluorobenzoyl)malonates and their thermal intramolecular cyclizat
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2011. - Vol.60, №5. - С. 929-932
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): polyfluorobenzoyl--polyfluorobenzoyl chlorides --cyclization
Аннотация: The reaction of the C-ethoxymagnesium derivative of diethyl malonate with polyfluorobenzoyl chlorides affords the corresponding (polyfluorobenzoyl)malonates prone to thermal cyclization into coumarin derivatives. The compounds obtained are inherent in keto—enol tautomerism
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2011, 60 (5), 929-932.pdf
Найти похожие

16.

Вид документа : Статья из журнала
Шифр издания : 54/S 83
Автор(ы) : Korotaev V.Yu., Sosnovskikh V. Ya., Barabanov M.A., Barkov A. Yu., Kodess M. I.
Заглавие : Stereoselective tandem [4 + 2]/[3 + 2] cycloaddition reactions of 3,3,3-trichloro(trifluoro)-1-nitropropenes and 2,3-dihydrofuran [Electronic resource]
Место публикации : Mendeleev Communications. - 2010. - Vol. 20, № 1. - С. 17-19
Систем. требования: http://www.sciencedirect.com/science/article/pii/S0959943610000088
Примечания : 12.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The first example of the domino hetero-Diels–Alder/1,3-dipolar cycloaddition, in which 3,3,3-trichloro(trifluoro)-1-nitropropenes act as both the heterodiene and the dipolarophile in the reaction with 2,3-dihydrofuran, is described. The trichloromethylated nitroolefin gave tricyclic nitroso acetal as a single regio- and stereoisomer, while the trifluoromethylated derivative afforded a 3:1 mixture of two regioisomeric cycloadducts
\\\\Expert2\\nbo\\Mendeleev Communications\\2010, v.20, p.17.pdf
Найти похожие

17.

Вид документа : Статья из журнала
Шифр издания : 54/S 61
Автор(ы) : Petrova Yu. S., Neudachina L.K., Mechaev A., Pestov A. V.
Заглавие : Simple synthesis and chelation capacity of N-(2-sulfoethyl)chitosan, a taurine derivative [Электронный ресурс]
Место публикации : Carbohydrate Polymers. - 2014. - Vol.112. - С. 462-468
Систем. требования: http://libgen.org/scimag/get.php?doi=10.1016%2Fj.carbpol.2014.06.028
Примечания : Bibliogr. : p. 467-468 (60 ref.). - 13.08.2014
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): chitosan--selectivity--sorption
Аннотация: This study presents a simple and effective synthesis method of N-(2-sulfoethyl)chitosan (NSE-chitosan) via a reaction between sodium 2-bromoethanesulfonate and chitosan that allows polymer transformation without using additional reagents and organic solvents. The chemical structure of the obtained NSE-chitosan was characterized by FT-IR and 1H NMR spectroscopies. Thermogravimetric study of NSE-chitosan coupled with FT-IR analysis has shown stability of the polymer up to 200 °C, which almost does not change with the increase of degree of substitution (DS). The sorption of transition and alkaline earth metal ions from multicomponent solutions on NSE-chitosan was investigated. The synthesized sorbents showed the selective recovery of silver(I) and copper(II) ions from ammonium acetate buffer solution. The increase of DS enhanced the selectivity to silver(I) ions sorption in comparison with copper(II) ions. Selectivity coefficients KAg/Cu increase from 1.3 to 10.9 with DS increasing up to 0.7 (ammonium acetate buffer solution, pH 6.5). Sorption isotherms of transition metal ions on NSE-chitosan with DS = 0.5 have been fitted using Langmuir, Freundlich, and Redlich-Peterson models. The maximum sorption capacities of sorbent in ammonium acetate buffer solution at pH 6.0 were 1.72 mmol/g for Cu(II), 1.23 mmol/g for Ag(I) and below 0.5 mmol/g for Co(II), Zn(II), Cd(II), Pb(II), Mn(II) and Ni(II) ions
\\\\expert2\\nbo\\Carbohydrate Polymers\\2014, v. 112, p. 462.pdf
Найти похожие

18.

Вид документа : Статья из журнала
Шифр издания : 54/S 45
Автор(ы) : Petrova Yu. S., Pestov A. V., Usoltseva M. K., Neudachina L.K.
Заглавие : Selective adsorption of silver(I) ions over copper(II) ions on sulfoethyl derivative of chitosan
Место публикации : Journal of Hazardous Materials. - 2015. - Vol. 299. - С. 696-701
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): selective adsorption--silver--copper (ii) complex
\\\\expert2\\NBO\\Journal of Hazardous Materials\\2015, v.299, p.696.pdf
Найти похожие

19.

Вид документа : Статья из журнала
Шифр издания : 54/S 45
Автор(ы) : Rozov F.N., Grinenko T.S., Levit G. L., Krasnov V. P., Belyavskii A.V.
Заглавие : Selection of genetically modified hematopoietic cells in vitro and in vivo using alkylating agent lysomustine
Место публикации : Analytical Biochemistry . - 2010. - Vol. 404, № 2. - С. 149-154
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Efficient gene transfer into hematopoietic stem cells is vital for the success of gene therapy of hematopoietic and immune system disorders. An in vivo selection system based on a mutant form of the O6-methylguanine-DNA-methyltransferase gene (MGMTm) is considered one of the more promising strategies for expansion of hematopoietic cells transduced with viral vectors. Here we demonstrate that MGMTm-expressing cells can be efficiently selected using lysomustine, a nitrosourea derivative of lysine. K562 and murine bone marrow cells expressing MGMTm are protected from the cytotoxic action of lysomustine in vitro. We also show in a murine model that MGMTm-transduced hematopoietic cells can be expanded in vivo on transplantation into sublethally irradiated recipients followed by lysomustine treatment. These results indicate that lysomustine can be used as a potent novel chemoselection drug applicable for gene therapy of hematopoietic and immune system disorders
Найти похожие

20.

Вид документа : Статья из журнала
Шифр издания : 54/S 10
Автор(ы) : Chupakhin O. N., Utepova I. A., Varaksin M. V., Tretyakov E. V., Romanenko G. V., Ovcharenko V., Stass D. V.
Заглавие : S-N(H) approach in the synthesis of nitronyl nitroxides
Место публикации : Journal of Organic Chemistry. - 2009. - Vol. 74, № 7. - С. 2870-2872
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
\\\\Expert2\\nbo\\Journal of Organic Chemistry\\2009, v.74, p.2870.pdf
Найти похожие

 1-20    21-40   41-56 
 

Сиглы отделов ЦНБ УрО РАН


  бр.ф. - Бронированный фонд

  бф - Научно-библиографический отдел

  БХЛ - Фонд художественной литературы

  ИИиА -Фонд исторической литературы в ЦНБ УрО РАН

  ИМЕТ -Отдел ЦНБ в Институте металлургии УрО РАН

  кх - Отдел фондов (книгохранениe)

  МБА - Межбиблиотечный абонемент

  мф - Методический фонд

  ок - Отдел научной каталогизации

  оку - Отдел комплектования и учета

  орф - Обменно-резервный фонд

  пф - Читальный зал деловой и патентной информации

  рк - Фонд редкой книги

  ч/з - Главный читальный зал

  эр - Зал электронных ресурсов

  

Сиглы библиотек институтов и НЦ УрО РАН
© Международная Ассоциация пользователей и разработчиков электронных библиотек и новых информационных технологий
(Ассоциация ЭБНИТ)
Яндекс.Метрика