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1.
Инвентарный номер: нет.
   
   Н 52


   
    Неожиданное превращение фторсодержащих CH-кислот при взаимодействии с хлоридом иода [] = Sudden conversion of fluorine-containing CH-acids during interaction with iodine chloride / В. Г. Пономарев, П. В. Подсевалов, Т. И. Назаренко, Л. Е. Деев, К. И. Пашкевич // Журнал органической химии. - 1990. - Т. 26, N 6. - С. 1365-1366 . - ISSN 0514-7492
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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2.
Инвентарный номер: нет.
   
   B 43


   
    Benzimidazo[l,2-a]pyrazolo[l,5-c]quinazoline: a novel heterocyclic system [Electronic resource] / G. N. Lipunova, G. A. Mokrushina, E. B. Granovskaya, O. M. Chasovskikh, V. N. Charushin // Mendeleev Communications. - 1996. - Vol. 6, № 1. - P15-17
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Heating of ethyl 3-[beta-(benzimidazol-2-yl)hydrazine]-2-(polyfluorobenzoyl)acrylates in acetonitrile with potassium fluoride or triethylbenzyl ammonium chloride leads to derivatives of novel heterocyclic systems of benzimidazo[l,2-a]pyrazolo- [1,5-c]quinazoline

\\\\expert2\\nbo\\Mendeleev Communications\\1996, v.6, N 1. p.15.pdf
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3.
Инвентарный номер: нет.
   
   P 51


   
    Petrological model of formation of giant ore deposits [Text] / A. A. Marakushev, N. A. Paneyakh, V. L. Rusinov, N. N. Pertsev, I. A. Zotov // Geology of Ore Deposits. - 1998. - Vol. 40, № 3. - P211-227. - Bibliogr. : p. 227 (46 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PETROLOGICAL MODEL -- MODELLING -- ORE -- ORE DEPOSITS
Аннотация: The available data on the giant ore deposits of chromium (Kempirsai in the Urals), platinum-group metals (Bushveld in Africa), platinum-bearing copper-nickel ores (Talnakh in the Noril'sk district, northern part of the Siberian Platform), zinc-copper (massive sulfide) ores (Gai, Sibai, and Uchaly) and apatite deposits (Khibiny, the Kola Peninsula) is summarized. The giant sizes of the deposits are caused by extraordinary ore-forming processes directly associated with the highly extensive petrogenetic processes. These processes resulted in the formation of peculiar dunites in the hyperbasite complexes (chromite ores), agpaitic urtites in alkaline associations (apatite deposits), development of low-sulfide horizons and hortonolite dunites in the basite-hyperbasite layered intrusions (platinum-group metal deposits), specific processes of transmagmatic sulfurization of the iron-rich igneous differentiates (Cu-Ni sulfide and massif sulfide ores), and processes of magmatic replacement of hyperbasites that cause the alkaline agpaitic affinity of magmatism. This agpaitic tendency increases the solubility of carbon-bearing fluid components (CO2, CH4, etc.) in magma and leads to the concentration of ore metals, which form chloride-carbonate and hydrocarbon migrating compounds in the transmagmatic fluids. Some mineralogical-petrological prospecting criteria are deduced on the basis of genetic models of giant ore deposits.

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4.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of ethyl 3-oxo-2-(3,4,5-trifluoro-2,6-dimethoxybenzoyl)butyrate [Electronic resource] / S. P. Kisil', M. I. Kodess, Ya. V. Burgart, V. I. Saloutin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2000. - Vol. 49, № 6. - P1090-1092
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Ethyl acetoacetate was acylated with 3,4,5-trifluoro-2,6-dimethoxybenzoyl chloride to give, for the first time, ethyl 3-oxo-2-(3,4,5-trifluoro-2,6-dimethoxybenzoyl)butyrate and its copper chelate. The title compound was used for the synthesis of 6,7,8-trifluoro-5-hydroxy-2-methylchromone, 1-(3,4,5-trifluoro-2,6-dimethoxyphenyl)butane-1,3-dione, and its copper chelate

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2000, 49 (6), 1090.pdf
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5.
Инвентарный номер: нет.
   
   A 10


   
    A route to ethyl alfa-pentafluorobenzoyl-beta-oxobutanoate via its copper(II) chelate [Text] / Ya. V. Burgart, S. P. Kisil', V. I. Saloutin, O. N. Chupakhin // Mendeleev Communications. - 2001. - Vol. 11, № 2. - P76
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Ethyl 2-pentafluorobenzoyl-3-oxobutanoate has been prepared by the acylation of ethyl acetoacetate with pentafluorobenzoyl chloride via a copper(II) chelate

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6.
Инвентарный номер: нет.
   
   K 46


   
    Kinetic resolution of Heterocyclic Amines using N-Tosyl-(S)-prolyl chloride [Text] : доклад, тезисы доклада / V. N. Charushin, V. P. Krasnov, G. L. Levit, I. N. Andreeva, I. M. Bukrina // XXth European Colloquium on Heterocyclic Chemistry, Stockholm,Sweden, 18-21 Aug. 2002 г. - Stockholm, 2002. - PA:7
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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7.
Инвентарный номер: нет.
   
   Z 99


    Zyryanov, G. V.
    Easy formation of S-N(H) products in reactions of indoles and pyrroles with 3-aryl-1,2,4-triazin-5(2H)-ones in the presence of tosyl chloride [Electronic resource] / G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2002. - Vol. 51, № 6. - P1042-1044
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of 3-aryl-1,2,4-triazin-5(2H)-ones with indoles and pyrroles in the presence of p-toluenesulfonyl chloride afforded 3-aryl-6-hetaryl-1,2,4-triazin-5(2H)-ones in high yields. The latter are products of the nucleophilic substitution of hydrogen

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2002, 51 (6), 1042-1044.pdf
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8.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of 4-acyl(alkoxycarbonyl)-5-fluoroalkyl-3,5-dihydroxyfuran-2(5H)-ones [Electronic resource] / M. V. Pryadeina, Ya. V. Burgart, K. I. Suslova, V. I. Saloutin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2002. - Vol. 51, № 9. - P1727-1730
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 4-Acyl(alkoxycarbonyl)-5-fluoroalkyl-3,5-dihydroxyfuran-2(5H)-ones were obtained for the first time by the reactions of fluoroalkyl-containing 1,3-diketones and 3-oxo esters with oxalyl chloride

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2002, 51 (9), 1727.pdf
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9.
Инвентарный номер: нет.
   
   E 54


   
    Enantiomers of 3-amino-1-methyl-1,2-dicarba-closo-dodecaborane [Text] / V. P. Krasnov, G. L. Levit, V. N. Charushin, M. I. Kodess, V. N. Kalinin, O. N. Chupakhin // Tetrahedron: Asymmetry . - 2002. - Vol. 13, № 16. - P1833-1835. - Bibliogr. : p. 1835 (6 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The enantiomers of 3-amino-1-methyl-1,2-dicarba-closo-dodecaborane were prepared by means of resolution of the racemic mixture via acylation by (S)-naproxen chloride followed by separation and subsequent acid hydrolysis of each of the diastereoisomeric amides. Partial racemization of enantiomeric 3-aminocarboranes was observed during acid hydrolysis

\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\2002, v.13, p.1833.pdf
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10.
Инвентарный номер: нет.
   
   K 46


   
    Kinetic resolution of (±)-2-methyl-1,2,3,4-tetrahydroquinoline and (±)-2-methylindoline [Electronic resource] / V. P. Krasnov, G. L. Levit, I. N. Andreeva, A. N. Grishakov, V. N. Charushin, O. N. Chupakhin // Mendeleev Communications. - 2002. - Vol. 12, № 1. - P27-28
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The acylation of racemic 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methylindoline by (S)-naproxen acyl chloride resulted in their kinetic resolution with the predominant formation of (S,S)-diastereoisomeric amides (de 78–76%), recrystallisation of which followed by acid hydrolysis gave individual (S)-isomers of heterocyclic amines????

\\\\expert2\\nbo\\Mendeleev Communications\\2002, v.12, N 1. p.27.pdf
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11.
Инвентарный номер: нет.
   
   K 46


   
    Kinetic resolution of (±)-2,3-dihydro-3-methyl-4H-1,4-benzoxazine, (±)-2-methyl-1,2,3,4-tetrahydroquinoline and (±)-2-methylindoline using N-tosyl-(S)-prolyl chloride [Text] / V. P. Krasnov, G. L. Levit, I. M. Bukrina, I. N. Andreeva, L. Sh. Sadretdinova, M. A. Koroleva, M. I. Kodess, V. N. Charushin, O. N. Chupakhin // Tetrahedron: Asymmetry . - 2003. - Vol. 14, № 14. - P1985-1988. - Bibliogr. : p. 1988 (6 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Acylation of racemic 2,3-dihydro-3-methyl-4H-1,4-benzoxazine, 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methylindoline with N-tosyl-(S)-prolyl chloride resulted in their kinetic resolution with the predominant formation of (R,S)-diastereoisomeric amides, des being 80, 66 and 38%, respectively. Recrystallisation of the amides followed by acid hydrolysis gave individual (R)-enantiomers of heterocyclic amines

\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\2003, v.14, p.1985.pdf
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12.
Инвентарный номер: нет.
   
   K 81


    Krasnykh, O. P.
    Synthesis of 5-alkyl-4-polyfluoroacylpyrrole-2,3(1H)-diones [Electronic resource] / O. P. Krasnykh, N. S. Karpenko, V. I. Filyakova // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 10. - P2340-2341 : ил. - Библиогр.: с. 2341 (9 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
FLUOROALKYL-CONTAINING BETA-AMINOVINYL KETONES -- OXALYL CHLORIDE -- PYRROLE-2,3(1h)-DIONES
Аннотация: Diacylation of fluoroalkyl-containing beta-aminovinyl ketones with oxalyl chloride afforded 5-alkyl-4-polyfluoroacylpyrrole-2,3(1H)-diones.

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (10), 2340.pdf
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13.
Инвентарный номер: нет.
   
   N 10


   
    N-Phthaloyl-(S)-alanyl chloride as a chiral resolving agent for the kinetic resolution of heterocyclic amines [Text] / V. P. Krasnov, G. L. Levit, M. I. Kodess, V. N. Charushin, O. N. Chupakhin // Tetrahedron: Asymmetry . - 2004. - Vol. 15, № 5. - P859-862 : ил. - Библиогр.: с. 862 (7 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HETEROCYCLIC AMINES -- CHLORIDE -- KINETIC RESOLUTION
Аннотация: Acylation of heterocyclic amines with N-phthaloyl-(S)-alanyl chloride under kinetic resolution conditions resulted in the predominant formation of (S,S)-amides. The diastereoselectivity of resolution depended heavily on the structure of the resolved amine.????

\\\\Expert2\\nbo\\Tetrahedron Asymmetry\\2004, v.15, p.859.pdf
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14.
Инвентарный номер: нет.
   
   K 46


   
    Kinetic resolution of (±)-2,3-dihydro-3-methyl-4H-1,4-benzoxazine in the reaction with (S)-naproxen chloride: A theoretical study [Electronic resource] / V. A. Potemkin, V. P. Krasnov, G. L. Levit, E. V. Bartashevich, I. N. Andreeva, M. B. Kuzminsky , N. A. Anikin, V. N. Charushin, O. N. Chupakhin // Mendeleev Communications. - 2004. - Vol. 14, № 2. - P69-70 : ил. - Библиогр.: с. 70 (14 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
KINETIC RESOLUTION -- CHLORIDE -- COMPUTATION METHODS
Аннотация: The kinetic resolution of (±)-2,3-dihydro-3-methyl-4H-1,4- benzoxazine by the action of (S)-naproxen chloride was theoretically studied based on various computation methods.

\\\\Expert2\\nbo\\Mendeleev Communications\\2004, v.14, p.69.pdf
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15.
Инвентарный номер: нет.
   
   K 46


   
    Kinetic resolution of 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-closo-dodecaboranes via acylation with chiral acyl chlorides [Electronic resource] / G. L. Levit, V. P. Krasnov, A. M. Demin, M. I. Kodess, L. Sh. Sadretdinova, T. V. Matveeva, V. A. Ol'shevskaya, V. N. Kalinin, O. N. Chupakhin, V. N. Charushin // Mendeleev Communications. - 2004. - Vol. 14, № 6. - P293-295
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A study of the kinetic resolution of racemic 1-substituted 3-amino-1,2-dicarba-closo-dodecaboranes by chiral acyl chlorides has shown that N-tosyl-(S)-prolyl and N-phthaloyl-(S)-alaninyl chlorides are more efficient resolving agents than (S)-naproxen chloride.

\\\\Expert2\\nbo\\Mendeleev Communications\\2004, v.14, p.293.pdf
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16.
Инвентарный номер: нет.
   
   U 62


   
    Unusual transformation of a fluoroalkyl-containing beta-aminovinyl ketone [Electronic resource] / O. P. Krasnykh, N. S. Karpenko, V. I. Filyakova, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 6. - P1355-1356 : ил. - Библиогр.: с. 1356 (3 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHLORIDE -- KETONE DERIVATIVE -- CYCLIZATION -- FLUOROALKYL-CONTAINING BETA-AMINOVINYL KETONE

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (6), 1355.pdf
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17.
Инвентарный номер: нет.
   
   F 70


   
    Fluorine-containing pyrido[1,2-a]quinazolin-6-ones [Electronic resource] / E. V. Nosova, G. N. Lipunova, M. I. Kodess, E. B. Vasil'eva, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 10. - P2314-2318
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of 2-aminopyridine and 2-amino-5-methylpyridine with 2,3,4,5-tetrafluorobenzoyl chloride afforded N,N’-diaroylpyridinium salts, which were converted into 6H-pyrido[1,2-a]quinazolin-6-ones by refluxing in toluene in the presence of triethylamine. The angular structure of the tricyclic derivatives obtained was confirmed by 19F and 13C NMR spectroscopy and 2D heteronuclear HetCOR and HMBC experiments

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (10), 2314.pdf
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18.
Инвентарный номер: нет.
   
   F 70


   
    Fluorine-Containing Heterocycles. XII. Fluorine-Containing Quinazolin-4-ones and Azolo[a]quinazolinone Derivatives [Electronic resource] / G. N. Lipunova, E. V. Nosova, A. A. Laeva, M. I. Kodess, V. N. Charushin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2005. - Vol. 41, № 7. - P1071-1080
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Methods for the synthesis of fluorine-containing derivatives of 2-imino-1,3-diphenylquinazolin-4-one, imidazo[1,2-a]quinazolin-5-one, pyrazolo[1,5-a]quinazolin-5-one, and [1,2,4]triazolo[1,5-a]quinazolin-5-one were developed on the basis of the reaction of tetrafluorobenzoyl chloride with N,N?-diphenylguanidine and aminoazoles

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2005, 41 (7), 1071.pdf
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19.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis, analgesic and antipyretic activity of 2-(antipyrin-4-yl)hydrazones of 1,2,3-triketones and their derivatives [Electronic resource] / E. V. Shchegol'kov, O. G. Khudina, L. V. Anikina, Ya. V. Burgart, V. I. Saloutin // Pharmaceutical Chemistry Journal. - 2006. - Vol. 40, № 7. - P373-376. - Библиогр. : с. 376 (10 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 1,2,3-Triketone 2-(antipyrin-4-yl)hydrazones were synthesized via the azo-coupling reactions of 1,3-diketones with 2-(antipyrin-4-yl)diazonium chloride. The fluoroalkyl-containing hetarylhydrazone enters into cyclocondensation with hydrazines at the 1,3-dicarbonyl fragment to yield 3-tetrafluoroethyl derivatives of pyrazole. It was found that 1,2,3-triketone 2-(antipyrin-4-yl)hydrazones and N-(2-hydroxyethyl)-substituted pyrazole exhibit analgesic activity comparable with that of their structural analog analgin (metamizole sodium), but do not possess antipyretic properties. In contrast, N-phenyl-substituted pyrazole did not exhibit analgesic properties but produced a certain antipyretic effect four hours after pyrogenic administration. Fluoroalkyl-containing compounds are less toxic substances than nonfluorinated 2-(antipyrin-4-yl)hydrazone and analgin.

\\\\Expert2\\nbo\\Pharmaceutical Chemistry Journal\\2006, 40 (7), 373-376.pdf
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20.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and antiviral activity of fluorinated 3-phenyl-1,2,4-benzotriazines [Electronic resource] / S. K. Kotovskaya, G. A. Zhumabaeva, N. M. Perova, Z. M. Baskakova, V. N. Charushin, O. N. Chupakhin, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova // Pharmaceutical Chemistry Journal. - 2007. - Vol. 41, № 2. - P62-68. - Библиогр. : с. 68 (18 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: New synthetic approaches to fluorinated 3-phenyl-1,2,4-benzotriazines for biological testing have been elaborated. 1-(3,4-Difluorophenyl)-3,5-diphenylformazan (IVa) was synthesized via dinitriding of 3,4-difluoroaniline, followed by azo-addition of the resulting azobenzenediazonium chloride with acetaldehyde phenylhydrazone. 6,7-Difluoro-3-phenyl-1,2,4-benzotriazine (Va) was obtained via intramolecular cyclization of formazan IVa in the presence of BF3/AcOH complex. Monofluoro-substituted 6-R-7-fluoro-3-phenyl-1,2,4-benzotriazine derivatives (Vb-Vq) were prepared by substituting fluorine atom with alkoxides in 3,4-difluoronitrobenzene. Conditions for nucleophilic substitution of the second fluorine atom in benzotriazines V have been established. Fluorinated 3-phenyl-1,2,4-benzotriazines have been tested for antiviral and cytotoxic activity on Vero cell cultures and proved to be active against severe diseases caused by smallpox and some other pathogenic viruses. ??

\\\\Expert2\\nbo\\Pharmaceutical Chemistry Journal\\2007, 41 (2), 62.pdf
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