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R. I. Vas’kevich P. V. Savitskii Yu. L. Zborovskii V. I. Staninets A. V. Turov A. N. Chernega 《Russian Journal of Organic Chemistry》2006,42(9):1396-1402
Reactions of substituted 1-(thieno[2,3-d]pyrimidin-2-yl)-4-arylthiosemicarbazides with methyl iodide led to the formation of fused triazolothienopyrimidine derivatives. 相似文献
4.
T. T. Kucherenko P. V. Muzyka É. B. Rusanov A. N. Chernega V. A. Kovtunenko A. K. Tyltin F. S. Babichev 《Chemistry of Heterocyclic Compounds》1992,28(5):515-518
An unusual path for the reaction of 2-aryl-1-dimethylamino-2H-isoindoles with N-R-maleimides, leading to the imides of l,2-dihydronaphthalene-2,3-dicarboxylic adds, was established by x-ray crystallographic analysis.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 614–618, May, 1992 相似文献
5.
O. B. Smolii L. V. Muzychka A. N. Chernega B. S. Drach 《Russian Journal of General Chemistry》2005,75(4):527-532
The substituted vinylphosphonium salt (E)-MeSCH=C(CN)P+Ph3I− readily cyclizes under the action of benzamidine and 3-amino-s-triazole, but it does not enter cyclocondensation with 2-aminopyridine. The structure of the cyclization product with 3-amino-s-triazole was confirmed by its transformation to 7-imino-6-(triphenylphosphoranylidene)-6,7-dihydro-s-triazolo[1,5]pyrimidine which was identified by X-ray diffraction. This stabilized ylide and its analogs proved useful starting materials for regioselective syntheses of 2-R-4-alkyl-4,7-dihydro-s-triazolo[1,5-a]pyrimidin-7-ones.__________Translated from Zhurnal Obshchei Khimii, Vol. 75, No. 4, 2005, pp. 565–570.Original Russian Text Copyright © 2005 by Smolii, Muzychka, Chernega, Drach. 相似文献
6.
Dmitriy M. Volochnyuk Dmitriy A. Sibgatulin Alexander N. Chernega 《Tetrahedron》2005,61(11):2839-2847
The reaction of 1,1,1,5,5,5-hexafluoroacetylacetone with push-pull enamines having a methyl group at the α-position was investigated. It was found that the reaction is sensitive both to the structure of enamines and to reaction conditions. As a result, a set of bistrifluoromethyldialkylanilines and ethyl bistrifluoromethylsalicylate was prepared. Plausible mechanisms and factors influencing the course of the reaction are discussed. 相似文献
7.
V. M. Timoshenko Ya. V. Nikolin A. N. Chernega E. B. Rusanov Yu. G. Shermolovich 《Chemistry of Heterocyclic Compounds》2001,37(4):470-476
The reaction of 1,1-dihydropolyfluoroalkyl benzyl sulfones with sodium azide or trimethylsilyl azide in the presence of tertiary amines gives ammonium salts of 4-benzylsulfonyl-5-polyfluoroalkyl--triazoles. The proposed reaction scheme includes the participation of catalytic amounts of azide ion in the cyclization of the formed intermediate vinyl azides to triazoles. X-ray analysis of 1,4-diazabicyclo[2.2.2]octane salt of 4-benzylsulfonyl-5-(-H-hexafluoropropyl)--triazole has been carried out. 相似文献
8.
Borisevich A. N. Samoilenko L. S. Lozinskii M. O. Rusanov E. B. Chernega A. N. 《Russian Journal of General Chemistry》2001,71(11):1767-1770
Reactions of acetylthioacetanilide with arylamines in acetic acid in the presence of sodium acetate give 3-arylaminothiocrotonanilides in good yields. When treated with -bromoacetophenone in acetone, these products are converted to substituted 4-hydroxy-2-thiazolinium bromides, one of which was dehydrated to obtain the corresponding thiazolium bromide. The structure of the heterocyclization products was confirmed by single crystal X-ray diffraction and NMR study of 2-acetonylidene-3,4-diphenyl-2,3-dihydrothiazole formed by dehydration of the corresponding 2-thiazolinium salt with simultaneous hydrolysis. 相似文献
9.
V. V. Dotsenko S. G. Krivokolysko A. N. Chernega V. P. Litvinov 《Russian Chemical Bulletin》2007,56(7):1431-1436
A new stereoselective method for the synthesis of trans-isomers of 2-amino-4-aryl-5-benzoyl-4,5-dihydrothiophene-3-carbonitriles was proposed. The method involves base-catalyzed
reactions of phenacyl thiocyanate with 3-(het)aryl-2-cyanoprop-2-enethioamides. (4R,5S/4S,5R)-2-Amino-5-benzoyl-4-(2-chlorophenyl)-4,5-ihydrothiophene-3-carbonitrile was structurally characterized by X-ray diffraction
analysis.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1379–1383, July, 2007. 相似文献
10.
Condensation of propanal with cyanothioacetamide and morpholine gave 3-cyano-4-ethyl-5-methyl-6-morpholino-2-piperidone, the
structure of which was studied by X-ray analysis. Reaction of propanal with cyanothioacetamides and cycloalkanone enamines
gave 3-cyano-4-ethyl-2,5,6,7-tetrahydropyrindin-2(1H)-one and 3-cyano-4-ethyl-5,6-hexamethylenepyridine-2(1H)-thione. The
latter was used for the preparation of substituted 2-benzyloxycarbonylmethylthiopyridine and 3-amino-2-benzyloxycarbonylthieno[2,3-b]pyridine.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 1053–1059, July, 2005. 相似文献