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 Найдено в других БД:Публикации Чарушина В.Н. (54)
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1.
Инвентарный номер: нет.
   
   U 62


   
    Unusual ring-chain tautomerism in bicyclo[4.2.0]octane derivatives [Text] / V. Yu. Korotaev, A. Yu. Barkov, P. A. Slepukhin, M. I. Kodess, V. Ya. Sosnovskikh // Tetrahedron Letters. - 2011. - Vol. 52, № 23. - P3029-3032 : рис.
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A new type of ring-chain tautomerism, which consists of the reversible conversion of bicyclo[4.2.0]octane derivatives into trisubstituted enamines was found and studied by 1H NMR spectroscopy. The starting materials were prepared by the stereoselective reaction of (E)-3,3,3-trichloro-1-nitropropene with cyclohexanone enamines

\\\\Expert2\\nbo\\Tetrahedron Letters\\2011, v. 52, p. 3029.pdf
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2.
Инвентарный номер: нет.
   
   R 30


   
    Reactions of bromine-containing organozinc compounds derived from alfa,alfa-dibromo ketones with 2-arylmethylideneindan-1,3-diones and 5-arylmethylidene-2,2-dimethyl-1,3-dioxane-4,6-diones [Electronic resource] / V. V. Shchepin, Yu. G. Stepanyan, P. S. Silaichev, M. A. Ezhikova, M. I. Kodess // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2010. - Vol. 46, № 4. - P499-502 : il. - Bibliogr. : p. 502 (3 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BROMINE-CONTAINING ORGANOZINC COMPOUNDS -- BROM -- ZINK -- KETONES -- DIONES
Аннотация: Bromine-containing organozinc compounds generated from 1,1-dibromo-3,3-dimethylbutan-2-one reacted with 2-arylmethylideneindan-1,3-diones and 5-arylmethylidene-2,2-dimethyl-1,3-dioxane-4,6-diones to give 3-aryl-2-(2,2-dimethylpropanoyl)spiro[cyclopropane-1,2'-indan]-1',3'-diones and 1-aryl-6,6-dimethyl-2-(2,2-dimethylpropanoyl)-5,7-dioxaspiro[2.5]octan-4,8-diones, respectively. Reactions of 2-arylmethylideneindan-1,3-diones with bromine-containing zinc enolates derived from 1-aryl-2,2-dibromopropan-1-ones and 2,2-dibromo-1,2,3,4-tetrahydronaphthalen-1-one resulted in the formation of 2-aroyl-3-aryl-2-methylspiro-[cyclopropane-1,2'-indan]-1',3'-diones and 2,3: 8,9-dibenzo-12-phenyldispiro[4.0.5.1]dodecane-1,4,7-trione, respectively.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2010, 46 (4), 499-502.pdf
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3.
Инвентарный номер: нет.
   
   S 73


    Sosnovskikh, V. Ya.
    On the reaction of 3-cyanochromones with phenyl- and methylhydrazines: Structural revision and a simple synthesis of chromeno[4,3-c]pyrazol-4-ones [Text] / V. Ya. Sosnovskikh, V. S. Moshkin, M. I. Kodess // Journal of Heterocyclic Chemistry. - 2010. - Vol. 47, № 3. - P629-633
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of 3-cyanochromones with phenylhydrazine gave the corresponding 5-amino-4-salicyloyl-1-phenylpyrazoles, 2-aminochromone-3-carbaldehyde N-phenylhydrazones, and 1-phenylchromeno[4,3-c]pyrazol-4(1H)-one, depending on the reaction conditions. With methylhydrazine, 3-(2-hydroxyaryl)-1-methylpyrazole-4-carbonitriles and 2-methylchromeno[4,3-c]pyrazol-4(2H)-ones were obtained in moderate to high yields

\\\\Cserver\\dist\\НБО\\Электронная библиотека_Библиогр1\\Journal of Heterocyclic Chemistry\\2010.v.47.p.629.pdf
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4.
Инвентарный номер: нет.
   
   R 30


   
    Reactions of 3-aminoisoxazolo[4,5-c]coumarin with benzoyl chloride: the first example of a preparative 1,2,4-oxadiazole–oxazole rearrangement [Electronic resource] / V. Ya. Sosnovskikh, V. S. Moshkin, M. Yu. Kornev, M. I. Kodess // Mendeleev Communications. - 2011. - Vol. 21, № 2. - P110-111. - Bibliogr. : p. 111 (7 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Depending on conditions, reaction of 3-amino-4H-chromeno[3,4-d]isoxazol-4-one with benzoyl chloride gives 4-hydroxy- and/or 4-benzoyloxy-3-(5-phenyl-1,2,4-oxadiazol-3-yl)coumarins, which are rearranged into 2-benzamido-4H-chromeno[3,4-d]oxazol-4-one by heating in DMSO

\\\\Expert2\\nbo\\Mendeleev Communications\\2011, v.21, p.110.pdf
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5.
Инвентарный номер: нет.
   
   S 45


   
    Selective mоnо-N-2-carboxyethylation of chitosan in the presence of magnesium halides [Text] / A. V. Pestov, M. I. Kodess, E. G. Matochkina, Yu. G. Yatluk // Carbohydrate Polymers. - 2011. - Vol. 86, № 2. - P783-788. - Bibliogr. : p. 787-788 (19 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The solubility of chitosan in aqueous solutions of lithium and magnesium halides varies in the order: LiCl LiBr LiI; MgCl2 MgBr2 MgI2. A method for selective production of mono-N-(2-carboxyethyl)chitosan (NCE-chitosan) was developed by synthesis in gel (concentration of chitosan 4-20%) of the magnesium halides solution (1.1-3.5 M) using acrylic acid. Using for reaction of MgI2 or MgBr2 provides relative greater amount of the monosubstituted amino groups (73-87%) in comparison with their absence (50-70%) at the high degree of substitution (DS) more than 0.7. DS of the prepared NCE-chitosan and the ratios mono-: disubstitution of amino groups was determined by 1H NMR spectroscopy. The chemical structure of the obtained NCE-chitosan was characterized by FT-IR and 13C NMR spectroscopies

\\\\Expert2\\nbo\\Carbohydrate Polymers\\2011, v. 86, p.783.pdf
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6.
Инвентарный номер: нет.
   
   D 53


   
    Diastereoselective reactions of 1,1,1-trichloro(trifluoro)-3-nitrobut-2-enes with 2-morpholinoalk-1-enes [Electronic resource] / V. Yu. Korotaev, A. Yu. Barkov, P. A. Slepukhin, M. I. Kodess, V. Ya. Sosnovskikh // Mendeleev Communications. - 2011. - Vol. 21, № 2. - P112-114. - Bibliogr. : p. 114 (12 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of (E)-1,1,1-trichloro(trifluoro)-3-nitrobut-2-enes with 3,3-dimethyl-2-morpholinobutene in benzene give (4R*,6R*)-6-tert-butyl-3-methyl-6-morpholino-4-trihalomethyl-5,6-dihydro-4H-1,2-oxazine 2-oxides. In a dichloromethane solution, these cyclic nitronates undergo diastereoselective ring opening to produce nitroalkylated anti-CCl3- and syn-CF3-enamines, which are hydrolysed with dilute HCl to afford the respective anti-CCl3- and syn-CF3-g-nitroketones

\\\\Expert2\\nbo\\Mendeleev Communications\\2011, v.21, p.112.pdf
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7.
Инвентарный номер: нет.
   
   C 91


   
    Crystal structure of N-(3-hydroxypropyl)-beta-alanine and Bis(N-(3-hydroxypropyl)-beta-alaninato)dicopper(II) [Cu2 (Pro-ala)2] [Electronic resource] / A. V. Pestov, P. A. Slepukhin, L. S. Molochnikov, M. A. Ezhikova, M. I. Kodess, Yu. G. Yatluk // Russian Journal of Inorganic Chemistry (Zhurnal Neorganicheskoi Khimii). - 2010. - Vol. 55, № 2. - P201-208
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: N-(3-Hydroxypropyl)-beta-alanine was synthesized by the reacti on of 3-aminopropanol with acrylic acid. From this ligand and basic copper carbonate, bis(N-(3-hydroxypropyl)-beta-alaninato)dicopper(II) [Cu2 (C6H11NO3)2] was obtained. The structures of the chelating agent and the copper complex were studied by X-ray diffraction. The Cu(II) coordination polyhedron is a distorted square pyramid. Each ligand forms six-membered ?-alaninate and propanolamine chelate rings. The propoxy group functions as a bridge. In the crystal structure, the molecules form intermolecular coordination bonds C=OCu, which are perpendicular to the layers. The EPR signal typical of dimeric copper complexes is not observed due to low occupancy of the excited paramagnetic triplet state. The weak paramagnetic signal from monomeric copper complex allowed recording of the 1H NMR spectrum of [Cu2 (Pro-ala) 2] with characteristic line broadening and contact shift. It follows from the obtained data that on dissolution, the complex dissociates by 40% to give monomeric copper complexes

\\\\Expert2\\nbo\\Russian Journal of Inorganic Chemistry\\2010, v. 55, N 2, с.201.pdf
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8.
Инвентарный номер: нет.
   
   C 74


   
    Complete 11B spectral assignment of 3-amino-1-methyl-1,2-dicarba-closo-dodecarborane [Text] : доклад, тезисы доклада / M. I. Kodess, M. A. Ezhikova, G. L. Levit, V. P. Krasnov, V. A. Ol'shevskaya, V. N. Kalinin, V. N. Charushin, O. N. Chupakhin // Eleventh International Conference on Boron Chemistry "IMEBORON XI", M., July 28-Aug.2, 2002 : abstracts. - M., 2002. - 113 (P-35)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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9.
Инвентарный номер: нет.
   
   R 30


   
    Reactions of sigma(H)-adducts of 1-ethyl-1,4-diazinium salts with arylalkynes as a one-step approach to pyrrolo[1,2-a]pyrazine derivatives [Electronic resource] / E. V. Verbitskiy, P. A. Slepukhin, M. A. Ezhikova, M. I. Kodess, G. L. Rusinov, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2009. - Vol. 58, № 6. - P1291-1293
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The O- and C-adducts of 5-aryl and 5-hetaryl-2,3-dicyano-1-ethylpyrazinium salts are hidden sources of ylides, which can be used for the cyclization with arylacetylenes giving rise to pyrrolo[1,2-a]pyrazines

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2009, 58 (6), 1291-1293.pdf
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10.
Инвентарный номер: нет.
   
   S 73


    Sosnovskikh, V. Ya.
    Reactions of 3-cyanochromones with primary amines: structures of the products [Electronic resource] / V. Ya. Sosnovskikh, V. S. Moshkin, M. I. Kodess // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2010. - Vol. 59, № 3. - P615-625
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
3-CYANOCHROMONES -- PRIMARY AMINES -- RECYCLIZATION
Аннотация: Reactions of 3-cyanochromones with primary aromatic amines in boiling benzene gave mixtures of Z- and E-3-arylamino-2-(2-hydroxyaroyl)acrylonitriles and 2-amino-3-(aryl-iminomethyl)chromones. The latter can easily be obtained in the individual state when the reaction is carried out in the presence of triethylamine. In the case of primary aliphatic amines, the open-chain reaction product immediately undergoes cyclization into 3-alkyliminomethyl-2-aminochromones. The structures of the products were examined by 1D and 2D 1H, 13C, and 15N NMR spectroscopy in DMSO-d6 and CDCl3

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2009, 59 (3), 615-625.pdf
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