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1.
Инвентарный номер: нет.
   
   L 79


   
    Liquid-phase oxidation of anthracene by hydrogen-peroxide in the presence of vanadium-oxide bronzes CuXV2O5 [Text] / S. Y. Men'shikov, A. V. Vurasko, L. A. Petrov, V. L. Volkov, A. A. Novoselova // Pet-Chem Equipment Corp. - 1992. - Vol. 32, N 2. - P128-130
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Vanadium oxide bronzes of the general formula CuXV2O5, where 0x1, catalyse the liquid-phase oxidation of anthracene H2O2. The anthracene conversion and the selectivity with respect to anthraquinone are maximum withing the region of beta- and xi-phases respectively close to the compositions CuO. 6V2O5 and CuO.95V2O5.

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2.
Инвентарный номер: нет.
   
   L 79


   
    Liquid-phase oxidation of anthracene by hydrogen-peroxide in the presence of heterogenized vanadyl acetylacetonate [Electronic resource] / S. Y. Men'shikov, A. V. Vurasko, L. A. Petrov, L. S. Molochnikov, A. A. Novoselova, Z. E. Skryabina, V. I. Saloutin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1992. - Vol. 41, N 4. - P619-622
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The synthesis of hetrogenized vanadyl acetylacetoonate was accomplished by alkylation of a chloromethylated styrene-divinylbenzene copolymer via activation by Co (II) complexes. The effect of heterogenization of the structure of the complexes and their catelytic properties in the peroxide oxidation of anthracene was investigated by kinetic studies and ERP spectroscopy

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1992, 41 (4), 619.pdf
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3.
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   Р 25


    Ратнер, В. Г.
    Окисление фторалкилзамещенных аллиловых спиртов - синтез фторсодержащих альфа,бета-эпоксикетонов [] = Oxidation of fluoroalkyl-substituted allylic alcohols: A synthesis of fluorinated alpha,beta-epoxyketones / В. Г. Ратнер, К. И. Пашкевич // Изв. АН. Сер. Химическая. - 1996. - N 3. - С. 680-683 . - ISSN 0002-3353
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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4.
Инвентарный номер: нет.
   
   S 59


   
    Sigma-adducts of 1,2,4-triazine 4-oxides with Nucleophiles. II.Oxidation and Elimination as Two Pathways of sigma-adducts Aromatization [Text] : доклад, тезисы доклада / O. N. Chupakhin, I. S. Kovalev, D. N. Kozhevnikov, V. L. Rusinov // International Memorial I.Postovsky Conference on Organic Chemisty, Ekaterinburg, March 17-20, 1998 : program and abstracts. - Ekaterinburg, 1998. - P80
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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5.
Инвентарный номер: нет.
   
   O-97


   
    Oxidation of -cysteine in oxygen-saturated aqueous solution in the presence of Cu(II)-containing adjusted polymers [Text] / S. Y. Men'shikov, A. V. Vurasko, L. S. Molochnikov, E. G. Kovaleva, A. A. Efendiev // Journal of Molecular Catalysis A: Chemical. - 2000. - Т. 158, № 1. - P447-451
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The influence of synthesis conditions of adjusted sorbents based on polyethylenepolyamine on catalytic properties of their Cu(II)-containing samples has been studied. It was shown that adjustment of sorbents leads to a significant increase in activity of Cu(II)-containing catalysts on their base.

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6.
Инвентарный номер: нет.
   
   D 62


   
    Direct modification of benzoannelated crown ethers with 1,2,4-triazin-5(2H)-one moieties [Text] / G. L. Rusinov, D. G. Beresnev, N. A. Itsikson, O. N. Chupakhin // Heterocycles. - 2001. - Т. 55, № 12. - P2349-2359
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A convenient method for one-step coupling of benzoannelated crown ethers with 1,2,4-triazinones based on the reaction of nucleophilic addition to unsubstituted carbon atom of the triazine ring has been worked out. It has been shown that the reaction of 3-substituted 1,2,4-triazin-5(2H)-ones (1) with benzocrown ethers (benzo-12-crown-4, benzo-15-crown-5, benzo-18-crown-6) in the presence of acetic or trifluoroacetic anhydride is accompanied by acylation of triazine ring and results in formation of 3-(1-acyl-5-oxo-1,4,5,6-tetrahydro-1,2,4-triazin-6-yl)benzocrown ethers (7-12). The latters were converted to 3-(5-oxo-2,5-dihydro-1,2,4-triazin-6-yl)benzocrown ethers (18-20) using two alternative routes: the elimination of acetic or trifluoroacetaldehyde or the deacylation followed by the oxidation of the 1,4,5,6-tetrahydro derivatives (13-15).

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7.
Инвентарный номер: нет.
   
   W 20


   
    Wall Rock Metasomatism and Formation Conditions of the Silver-Polymetallic Bol'shoi Kanimansur Deposit (Tadjikistan) [Text] / O. V. Rusinova, V. L. Rusinov, E. D. Syngaevskii , L. I. Bochek, M. I. Lapina, Yu. V. Vasyuta // Geology of Ore Deposits. - 2001. - Vol. 43, № 5. - P386-405. - Bibliogr. : p. 405 (20 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SILVER-POLYMETALLIC DEPOSIT -- CARBON -- METASOMATIC TRANSFORMATIONS -- REGIONAL MAGMATISM
Аннотация: Products of the hydrothermal alteration of rocks and vertical zonality at the Kanimansur silver-polymetallic deposit (Tadjikistan) have been studied. On the basis of these studies, physicocochemical conditions of metasomatism and ore formation were reviewed. Condensed carbonaceous matter in wall rock metasomatites and ores were found and carbon isotopic composition of this carbonaceous matter and composition of gases in open pores in rocks of the deposit were analyzed. As a result of geological observations, analysis of mineral parageneses, compositions of minerals, and chemistry of wall rock alteration, the following four stages of the hydrothermal process were distinguished: autometasomatic, propylitic, preore chlorite-sericite, and synore. Mineral geothermometers were used to estimate the temperatures of metasomatism, which varied within the range 200-250°C for all stages except for the autometasomatic stage (450-500°C). The formation of unhydrated light micas, quartz, and highly ferruginuous chlorites was related to acid preore metasomatism. The stability of these chlorites testifies to a slight increase in the acidity of solutions during the preore stage (pH not less than 3.5). The wall rock metasomatites and sulfide ores are characterized by a relatively rare occurrence of pyrite due to a low activity of the sulfide sulfur during hydrothermal alterations (logaS2 = -7...-10). The low activity of the sulfide sulfur is confirmed by the fact that iron is tied in a highly ferruginuous chlorite. At upper ore levels, even zinc is tied in chlorite. This testifies to a much greater aS2 /aO2 value. Judging by the participation of carbonaceous matter in the process, ore components were deposited due to a local increase in the alkalinity at the ore-forming stage and oxidation of reduced fluids. The established features of metasomatic transformations, are related to particulars of the regional magmatism.????

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8.
Инвентарный номер: нет.
   
   A 10


   
    A versatile strategy for the synthesis of functionalized 2,2 '-bi- and 2,2 ': 6 ',2 '-terpyridines via their 1,2,4-triazine analogues [Text] / V. N. Kozhevnikov, D. N. Kozhevnikov, T. V. Nikitina, V. L. Rusinov, O. N. Chupakhin, M. Zabel, B. Konig // Journal of Organic Chemistry. - 2003. - Vol. 68, № 7. - P2882-2888
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ALDEHYDES -- OXIDATION -- SUBSTITUTION REACTIONS
Аннотация: A general synthetic route for the synthesis of functionalized bi- and terpyridines is reported. Functionalized 1,2,4-triazene 4-oxides 7 and 8 - obtained from the reaction of hydrazones 1 with pyridine aldehydes and followed by oxidation - are functionalized by introduction of a cyano group via nucleophilic aromatic substitution. The thus-obtained 5-cyano-1,2,4-triazines 9 and 10 undergo facile inverse-electron-demand Diels-Alder reactions with enamines and alkenes to yield functionalized bi- and terpyridines, respectively. The substituent at position 6 of the 1,2,4-triazene 4-oxides must be aromatic or heteroaromatic in order to allow their facile synthesis, but other substituents and reagents may vary. Each step of the synthetic route allows diversification, which makes the approach particularly useful for the facile synthesis of a large variety of functionalized bi- and terpyridines.

\\\\Expert2\\nbo\\Journal of Organic Chemistry\\2003, v.68, N 7, p.2882. Chupakhin.pdf
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9.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of stereoisomeric 4-(2-methylindolin-1-yl)- and 4-(2-methylindol-1-yl) derivatives of glutamic acid [Electronic resource] / V. P. Krasnov, A. Yu. Vigorov, I. A. Nizova, A. N. Grishakov, N. G. Evstigneeva, M. I. Kodess // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 6. - P1327-1330
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reaction of dimethyl (2S,4RS)-N-phthaloyl-4-bromoglutamate with 2-methylindoline afforded diastereomeric 4-(2-methylindolin-1-yl)-(S)-glutamic acid derivatives, whose oxidation gave rise to 4-(2-methylindol-1-yl)-(S)-glutamic acid derivatives

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (6), 1327.pdf
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10.
Инвентарный номер: нет.
   
   Ч-54


   
    4,5-Difluoro-1,2-dehydrobenzene: generation and cycloaddition reactions [Electronic resource] / V. N. Charushin, S. K. Kotovskaya, S. A. Romanova, O. N. Chupakhin, Yu. V. Tomilov, O. M. Nefedov // Mendeleev Communications. - 2005. - Vol. 15, № 2. - P45-46
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CYCLOADDITION REACTIONS
Аннотация: The oxidation of 1-amino-5,6-difluorobenzotriazole with Pb(OAc)4 in dry CH2Cl2 afforded 4,5-difluoro-1,2-dehydrobenzene, a new active intermediate, which can be used in situ for the synthesis of fluorinated carbo- and heterocyclic compounds via cycloaddition reactions.

\\\\Expert2\\nbo\\Mendeleev Communications\\2005, v.15, p.45.pdf
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