Zobrazeno 1 - 10
of 103
pro vyhledávání: '"M. N. Zemtsova"'
Publikováno v:
Russian Journal of Organic Chemistry. 58:1569-1574
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e121cdbb8ddd827863892e1a3a862343
https://doi.org/10.1134/s1070428022110021
https://doi.org/10.1134/s1070428022110021
Publikováno v:
Russian Journal of Physical Chemistry A. 96:2246-2251
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9f409081a258fd7f7a70505df2db935
https://doi.org/10.1134/s0036024422100284
https://doi.org/10.1134/s0036024422100284
Autor:
M. R. Baimuratov, Yu. A. Gruzd, M. N. Zemtsova, Yu. N. Klimochkin, Yu. A. Golovko, S. V. Kulemina
Publikováno v:
Russian Journal of Organic Chemistry. 57:793-800
A convenient method of synthesis of fused heterocyclic systems, involving cyclization of the reaction products of 2-aryl-1,2,3,4-tetrahydroquinolines with triphosgene, chloroacetyl chloride, and oxalyl chloride in the presence of anhydrous AlCl3 in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7cea23b23260c079eaa7cd5f9b56794
https://doi.org/10.1134/s1070428021050055
https://doi.org/10.1134/s1070428021050055
Erratum to: Synthesis of Fused Heterocyclic Systems Derived from 2-Aryl-1,2,3,4-Tetrahydroquinolines
Autor:
M. N. Zemtsova, Yu. A. Golovko, Yu. A. Gruzd, S. V. Kulemina, M. R. Baimuratov, Yu. N. Klimochkin
Publikováno v:
Physics of Particles and Nuclei Letters. 19:81-81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::337f61009714898707f330444004749e
https://doi.org/10.1134/s1547477122010113
https://doi.org/10.1134/s1547477122010113
Publikováno v:
Russian Journal of Physical Chemistry A. 90:2471-2476
Regularities of the sorption of 1,2,3,4-tetrahydroquinoline derivatives on octadecylsilyl silica gel and porous graphitic carbon from aqueous acetonitrile solutions were investigated. The effect the molecular structure and physicochemical parameters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03dd4d0ce203e879d99c02328c87c7f7
https://doi.org/10.1134/s0036024416120220
https://doi.org/10.1134/s0036024416120220
Publikováno v:
Russian Journal of Organic Chemistry. 51:636-639
Bromination of 2-phenyltetrahydroquinolines derivatives was investigated. During the bromination of 2-phenyl-1,2,3,4-tetrahydroquinoline with bromine in chloroform or bromosuccinimide along with the formation of di- and tribrom derivatives the oxidat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e65571718d5eb3d76c9f0980bb15886b
https://doi.org/10.1134/s1070428015050085
https://doi.org/10.1134/s1070428015050085
Publikováno v:
Russian Chemical Reviews. 83:377-390
Examples of the synthesis of various heterocycles containing an adamantane moiety based on mono- and dicarbonyl adamantane derivatives are considered. Systems in which the adamantane cage is spiro-connected to a heterocyclic ring or is a part of subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e5cbd636123e73439cd2acde858b386
https://doi.org/10.1070/rc2014v083n05abeh004374
https://doi.org/10.1070/rc2014v083n05abeh004374
Publikováno v:
Russian Journal of Physical Chemistry A. 88:320-324
Regularities of the retention of certain 4-aminoquinoline derivatives in the conditions of the reversed phase type of high performance liquid chromatography (HPLC) on octadecyl silica (ODS) and hypercrosslinked polystyrene (HCLPS) are studied. The co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::709658f114c4c745982cf986907c707c
https://doi.org/10.1134/s0036024414020198
https://doi.org/10.1134/s0036024414020198
Synthesis and structure of methyl 8-allyl-6-bromo-2-methyl-1,2,3,4-tetrahydroquinoline-4-carboxylate
Publikováno v:
Crystallography Reports. 55:793-796
The compound C15H18NO2Br was synthesized and characterized by X-ray diffraction. The crystals belong to the monoclinic system, sp. gr. P21/n, a = 8.913(2) A, b = 23.637(6) A, c = 13.892(3) A, β = 90.31(2)°, Z = 8, V = 2926.8(12) A3, ρcalc = 1.472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfeb16c5da04c30aba86a1d7fc22dc27
https://doi.org/10.1134/s1063774510050123
https://doi.org/10.1134/s1063774510050123
Publikováno v:
Russian Journal of Organic Chemistry. 45:609-612
Reduction of some substituted quinoline-4-carboxylic acids was studied. The reduction of 2-alkylquinoline-4-carboxylic acids with Raney nickel in aqueous alkali was stereoselective, and the resulting 2-alkyl-1,2,3,4-tetrahydroquinoline-4-carboxylic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5078172ad84b956c268a2650f56bf61
https://doi.org/10.1134/s1070428009040228
https://doi.org/10.1134/s1070428009040228