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1.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and antituberculosis activity of novel 5-styryl-4-(hetero)aryl-pyrimidines via combination of the Pd-catalyzed Suzuki cross-coupling and SNH reactions [Electronic resource] / M. A. Kravchenko, E. V. Verbitskiy, I. D. Medvinskiy, G. L. Rusinov, V. N. Charushin // Bioorganic and Medicinal Chemistry Letters. - 2014. - Vol. 24, №14. - С. 3118-3120
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PYRIMIDINE -- ANTIMICOBACTERIAL -- TUBERCULOSIS
Аннотация: Combination of the Suzuki cross-coupling and nucleophilic aromatic substitution of hydrogen (SNH) reactions proved to be a convenient method for the synthesis of 5-styryl-4-(hetero)aryl substituted pyrimidines from commercially available 5-bromopyrimidine. All intermediate 5-bromo-4-(hetero)aryl substituted pyrimidines and also the targeted 5-styryl-4-(hetero)arylpyrimidines were found to be active in micromolar concentrations in vitro against Mycobacterium tuberculosis H37Rv, avium, terrae, and multi-drug-resistant strain isolated from tuberculosis patients in Ural region (Russia). It has been found that some of these compounds possess a low toxicity and have a bacteriostatic effect, comparable and even higher with that of first-line antituberculosis drugs

\\\\expert2\\nbo\\Bioorganic and Medicinal Chemistry Letters\\2014, v. 24, p. 3118.pdf
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2.
Инвентарный номер: нет.
   
   T 44


   
    The synthesis of polyarene-modified 5-phenyl-2,2'-bipyridines via the methodology and aza-Diels-Alder reaction [Electronic resource] / I. S. Kovalev, D. S. Kopchuk, A. F. Khasanov, V. L. Rusinov, O. N. Chupakhin // Mendeleev Communications. - 2014. - Vol.24, №2. - С. 117-118. - Bibliogr. : p. 118 (52 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
TRIAZINE -- LIGANDS -- ARENES
Аннотация: Nucleophilic substitution of hydrogen () in 6-phenyl-3-(2-pyridyl)-1,2,4- triazine under the action of lithium derivatives of polynuclear arenes followed by aza-Diels-Alder reaction with norbornadiene or morpholinocyclopentene gives the novel polyarenemodified photoluminescent 5-phenyl-2,2'-bipyridine ligands

\\\\expert2\\nbo\\Mendeleev Communications\\2014, v.24, p. 117-118.pdf
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3.
Инвентарный номер: нет.
   
   S 90


   
    Study of the supramolecular structures of complexes of carborane-containing pyridazines with 2,3,5,6-tetrachloro-1,4-dihydroxybenzene [Electronic resource] / P. A. Slepukhin, S. G. Tolshchina, A. V. Ignatenko, E. F. Zhilina, V. N. Charushin // Crystallography Reports. - 2014. - Vol.59, №2. - С. 202-206. - Bibliogr. : p. 206 (9 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PYRIDAZINES -- HETEROCYCLIC SUBSTITUENTS -- CARBORANE MOIETY
Аннотация: The structures and characteristic features of the molecular packing patterns of complexes of pyridazines containing heterocyclic substituents and the carborane moiety with 2,3,5,6-tetrachlorohydroquinone (TCHQ) were investigated. It was shown that TCHQ can form supramolecular assemblies with carborane-containing substituted pyridazines. The stoichiometry and three-dimensional structures of these assemblies depend on the substituents in the pyridazine ring and are formed via O-H⋯N hydrogen bonding between TCHQ and heterocyclic molecules

\\\\expert2\\NBO\\Crystallography Reports (Кристаллография)\\2014, v.59, N 2, p.202-206.pdf
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4.
Инвентарный номер: нет.
   
   N 91


   
    Nucleophilic dimerization of indoline under oxidative conditions [Electronic resource] / I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin // Mendeleev Communications. - 2014. - Vol.24, №1. - С. 40-41. - Bibliogr. : p. 41 (10 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
INDOLINE -- HYDROGEN PEROXIDE -- METHANOL
Аннотация: Oxidation of indoline with 30% hydrogen peroxide in methanol in the presence of sodium tungstate affords the dimeric 3-oxo-1’H,3H- 2,3’-biindole-1-oxide.

\\\\expert2\\nbo\\Mendeleev Communications\\2014, v.24 (1), p. 40.pdf
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5.
Инвентарный номер: нет.
   
   P 99


   
    Pyrolysis of polyolefins in high-boiling solvents [Электронный ресурс] / E. Andreikov, I. S. Amosova, Yu. A. Dikovinkina, M. G. Pervova // Solid Fuel Chemistry. - 2013. - Vol.47, №4. - С. 209-219. - Bibliogr. : p. 218-219 (47 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ALIPHATIC HYDROCARBONS -- COAL TAR PITCH -- HIGH-BOILING SOLVENTS
Аннотация: The pyrolysis of polyethylene and polypropylene in vacuum residue and coal-tar pitch solvents was studied in a batch reactor at atmospheric pressure in a temperature range of 380-420 °C. Aliphatic hydrocarbons and C 5-C32 normal olefins and isoolefins were the main pyrolysis products of the polyolefins and vacuum residue, which also underwent thermal degradation at these temperatures. The total conversion of a polypropylene-vacuum residue mixture into gaseous and distillate products was nearly additive; upon the pyrolysis of polypropylene in pitch and of polyethylene in vacuum residue and pitch, the yield of distillate products decreased and the paraffin/olefin ratio in these products increased. The observed regularities were explained by hydrogen transfer from the solvents to the intermediate radical products of the thermal decomposition of polymer chains. The reactions of the resulting of olefins with the solvents can also occur to a lesser degree. The greatest deviations from additivity were observed in the pyrolysis of polyethylene in the solvents used

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6.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of 4-(thien-2-yl)-substituted coumarins through Lewis acid catalyzed Michael addition of thiophenes to 3-benzoylcoumarins followed by oxidation [Electronic resource] / R. A. Irgashev, A. A. Karmatsky, G. L. Rusinov, V. N. Charushin // Tetrahedron Letters. - 2014. - Vol.55, №26. - С. 3603-3606
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
THIOPHENES -- 3-BENZOYLCOUMARINS -- Lewis acid
Аннотация: 3-Benzoyl-4-(thien-2-yl)coumarins have been obtained in good yields according to the SNH addition–oxidation protocol, involving the diastereoselective addition of thiophenes at C-4 of 3-benzoylcoumarins under BBr3 catalysis, followed by oxidation of the intermediate 3,4-trans-3-benzoyl-4-(thien-2-yl)-3,4-dihydrocoumarins with DDQ. This two-step procedure can be regarded as nucleophilic substitution of hydrogen (SNH) on the heterocyclic ring of coumarins

\\\\expert2\\nbo\\Tetrahedron Letters\\2014, v. 55, p. 3603.pdf
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7.
Инвентарный номер: нет.
   
   S 90


   
    Study of the supramolecular structures of complexes of carborane-containing pyridazines with 2,3,5,6-tetrachloro-1,4-dihydroxybenzene [Electronic resource] / P. A. Slepukhin, S. G. Tolshchina, N. K. Ignatenko, R. I. Ishmetova, G. L. Rusinov, E. F. Zhilina, V. N. Charushin // Crystallography Reports. - 2014. - Vol. 59, № 2. - С. 202-206. - Bibliogr. : p. 206 (9 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
MOLECULAR PACKING PATTERNS -- PYRIDAZINES CONTAINING HETEROCYCLIC SUBSTITUENTS -- TETRACHLOROHYDROQUINONE
Аннотация: The structures and characteristic features of the molecular packing patterns of complexes of pyridazines containing heterocyclic substituents and the carborane moiety with 2,3,5,6-tetrachlorohydroquinone (TCHQ) were investigated. It was shown that TCHQ can form supramolecular assemblies with carborane-containing substituted pyridazines. The stoichiometry and three-dimensional structures of these assemblies depend on the substituents in the pyridazine ring and are formed via O-H…N hydrogen bonding between TCHQ and heterocyclic molecules

\\\\expert2\\nbo\\Crystallography Reports (Кристаллография)\\2014, v.59, N 2, p.202-206.pdf
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8.
Инвентарный номер: нет.
   
   A 23


   
    Aerobic oxidative C-H/C-H coupling of azaaromatics with indoles and pyrroles in the presence of TiO2 as a photocatalyst [Electronic resource] / I. A. Utepova, M. A. Trestsova, O. N. Chupakhin, V. N. Charushin, A. A. Rempel // Green Chemistry. - 2015. - Vol. 17, № 8. - С. 4401-4410. - Bibliogr. : p. 4409-4410 (30 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BOND ACTIVATION -- INHIBITORS -- HYDROGEN
Аннотация: In this paper we wish to report a highly selective and benign method for the double C-H/C-H coupling of azaaromatics with indoles or pyrrole in the presence of air oxygen/TiO2, as an effective photocatalytic oxidative system. It has been shown that this versatile approach can be applied for direct C-H functionalisation of a variety of azaaromatic systems, such as mono-, di- and triazines, substituted and unsubstituted azines and their benzo-annelated analogues.

\\\\expert2\\nbo\\Green Chemistry\\2015, v.17, N 8, p.4401-4410.pdf
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9.
Инвентарный номер: нет.
   
   P 49


    Pestov, A. V.
    Copper and nickel chelate complexes with polydentate N,O-ligands: structure and magnetic properties of polynuclear complexes [Electronic resource] / A. V. Pestov, P. A. Slepukhin, V. N. Charushin // Russian Chemical Reviews. - 2015. - Vol. 84, № 3. - С. 310-333. - Bibliogr. : p. 331-333(182 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HYDROGEN-BONDED BRIDGES -- RAY CRYSTAL-STRUCTURE -- SCHIFF-BASE LIGAND
Аннотация: A comparative analysis of the structures of copper(II) and nickel(II) chelate complexes with N-substituted 2-aminoethanols, 3-aminopropan- 1 -ols, glycines and beta-alanines is performed. It is shown that tetradentate ligands based on 3-aminopropan- 1 -ol and P-alanine, sterically hindered 2-aminoethanol derivatives and tridentate enamino ketone derivatives tend to form oligonuclear copper(II) and nickel(II) complexes. Glycine derivatives do not provide the formation of oligonuclear copper(II) and nickel(II) complexes. The magnetic properties of a number of polynuclear complexes are compared.

\\\\expert2\\nbo\\Russian Chemical Reviews\\2015, V.84, N3, p. 310-333.pdf
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10.
Инвентарный номер: нет.
   
   O-72


   
    Organolithium compounds in the nucleophilic substitution of hydrogen in arenes and hetarenes [Electronic resource] / I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, V. N. Charushin // Russian Chemical Reviews. - 2015. - Vol. 84, № 12. - С. 1191-1225. - Bibliogr. : p. 1224-1225 (237 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
NUCLEOPHILIC SUBSTITUTION -- HYDROGEN -- ARENES AND HETARENES
Аннотация: The review considers the most typical examples of the direct non-activated non-catalytic C–C bond formation in arenes and their metal complexes activated by electron-withdrawing substituents in the aromatic nucleus and in hetarenes (azines and their N-oxides, porphyrins, etc.) upon the reactions with aliphatic and (hetero)aromatic (hetero)organolithium nucleophiles. Particular attention is given to the direct introduction of nitroxide radicals and (hetero)organic moieties into mono-, di- and triazines and their N-oxides. The influence of the structures of the (hetero)aromatic substrate and the (hetero)organolithium nucleophile on the reaction pathway and rate and on the structure of the reaction product is analyzed.

\\\\expert2\\nbo\\Russian Chemical Reviews\\2015, V.84, N12, p. 1191-1225.pdf
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