Works matching IS 10704280 AND DT 2016 AND VI 52 AND IP 12
Results: 30
Conversion of carbon dioxide to propionaldehyde over cobalt and rhodium nanoparticles supported on MIL-53 (Al) metal-organic framework.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1728, doi. 10.1134/S1070428016120022
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Efficient methods of synthesis of unsaturated alcohols and ketones by allylation of Favorsky reaction products under phase transfer conditions.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1733, doi. 10.1134/S1070428016120034
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Synthesis and bromination/dehydrobromination of N,N-diallyltrifluoromethanesulfonamide.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1738, doi. 10.1134/S1070428016120046
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Reaction of 3-carene with perfluoroalkanoic acids.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1743, doi. 10.1134/S1070428016120058
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Cycloalumination of allylbenzenes with triethylaluminum in the presence of CpZrCl. One-pot synthesis of 2-benzylbutane-1,4-diols as precursors of dibenzylbutane lignans.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1750, doi. 10.1134/S107042801612006X
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Steric effects in the catalytic amination of γ-, δ-, and ε-glycols.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1756, doi. 10.1134/S1070428016120071
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Synthesis of methyl 4-aryl-2-{[4-(carbamimidoylsulfamoyl)- phenyl]amino}-4-oxobut-2-enoates.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1762, doi. 10.1134/S1070428016120083
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Practical F/Δ-D transformation in the prostaglandin series. synthesis of methyl (±)-(5Z,12 E,14 E)-9α-acetoxy- 16-(3-chlorophenoxy)-15-deoxy-11-oxo-17,18,19,20-tetranorprosta- 5,12,14-trienoate from cloprostenol.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1765, doi. 10.1134/S1070428016120095
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Mass spectra of new heterocycles: XV. Fragmentation of 1-substituted 3-alkoxy-2-(propargylsulfanyl)- and 3-alkoxy-2-(allenylsulfanyl)-1 H-pyrroles under electron impact.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1773, doi. 10.1134/S1070428016120101
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Synthesis of spiro[imidazole-2,2′-pyrroles] by reaction of 4,5-dioxo-4,5-dihydro-1 H-pyrrole-2-carboxylates with urea.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1779, doi. 10.1134/S1070428016120113
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Reductive alkylation of disulfides. Synthesis of 2-(alkylsulfanyl)-1 H-pyrrole-3-carbonitriles.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1784, doi. 10.1134/S1070428016120125
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Synthesis of new functionally substituted hetarylcarbamates from methyl {4-[(2 E)-3-(4-methoxyphenyl)-prop-2-enoyl]phenyl}carbamate.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1788, doi. 10.1134/S1070428016120137
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Synthesis of 5-(Benzylamino)- exo-3-azatricyclo-[5.2.1.0]decan-4-one derivatives.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1792, doi. 10.1134/S1070428016120149
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Reaction of nitroanilines with aldehydes. Refinement of the Doebner-Miller reaction mechanism.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1797, doi. 10.1134/S1070428016120150
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Reaction of cytisine with alka-1,3- and -2,3-dien-2-ylphosphonates.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1804, doi. 10.1134/S1070428016120162
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Synthesis of 3-methyl-3,4-dihydroisoquinolines based on myristicin.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1812, doi. 10.1134/S1070428016120174
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Reaction of 2-chloromethylphenols with enaminones.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1817, doi. 10.1134/S1070428016120186
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Design and synthesis of imidazo[4,5- c]pyridine derivatives as promising Aurora kinase A (AURKA) inhibitors.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1822, doi. 10.1134/S1070428016120198
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Synthesis of 3-aminopyrazolo[3,4- b]pyridine-4-carbonitriles.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1830, doi. 10.1134/S1070428016120204
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Dimethyl ether in nanotubes: Structural variations and conformational preferences.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1835, doi. 10.1134/S1070428016120216
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Regio- and stereoselective synthesis of trichloro[( Z)-2-chloroalk-1-enyl]tellanes.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1842, doi. 10.1134/S1070428016120228
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Short and efficient synthetic route to lembehyne B possessing neuritogenic activity.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1844, doi. 10.1134/S107042801612023X
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Ecotoxicity of organic stabilizers for metal nanoparticles.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1847, doi. 10.1134/S1070428016120241
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Catalytic effect of molecular iodine in the pyrrolization of tetramethoxytetrahydrofuran with optically active amines.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1849, doi. 10.1134/S1070428016120253
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(3 Z)-2-azahexa-1,3,5-trienes: Generation and regioselectivity of 1,5- and 1,6-cyclizations.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1851, doi. 10.1134/S1070428016120265
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Synthesis of 3,7,9-triazatricyclo[6.2.1.0]undeca-2,4-dienes by reaction of 2-oxa-7-azaspiro[4.4]nona-3,6,8-trienes with sodium hydroxide.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1854, doi. 10.1134/S1070428016120277
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Opening of the pyridine ring in the system 1,1,1-trifluoro-4-phenylbut-3-yn-2-one-water. Stereoselective synthesis of 5-{[(1 Z)-4,4,4-trifluoro-3-oxo-1-phenylbut-1-en-1-yl]amino}penta-2,4-dienal.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1857, doi. 10.1134/S1070428016120289
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Synthesis of substituted 3,4-dihydrofuro[2,3- d]pyrimidines from 3-arylmethylidenefuran-2(3 H)-ones.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1861, doi. 10.1134/S1070428016120290
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Enantioselectivity of the reaction of α-amino acids with sodium azide and triethyl orthoformate in the synthesis of tetrazoles.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1863, doi. 10.1134/S1070428016120307
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Polystyrene-supported cu(II)-R-Box as recyclable catalyst in asymmetric Friedel-Crafts reaction.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 12, p. 1717, doi. 10.1134/S1070428016120010
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