Zobrazeno 1 - 10 of 13 pro vyhledávání: '"V. Yu. Tyutin"'
1
A novel three-component reaction of 1, 1-dicyano-2-(trifluoromethyl)ethylenes, primary arylamines, and ketones
Autor: N. D. Chkanikov, V. Yu. Tyutin, M. Yu. Antipin, A. V. Fokin, A. F. Kolomiets, Yu. T. Struchkov, V. N. Nesterov
Publikováno v: Russian Chemical Bulletin. 42:512-521
1, 1-Dicyano-2, 2-bis(trifluoromethyl)ethylene and 3, 3-dicyano-2-(trifluoromethyl)acrylates react with primary arylamines in the presence of ketones to form 1, 1-aryl-1, 4-dihydropyridme derivatives under mild conditions. The mechanism of this three
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6e61e5bb9715da988cb95ac3660bec3a
https://doi.org/10.1007/bf00698443
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4
ChemInform Abstract: Hexafluoroacetone and Methyl Trifluoropyruvate as Precursors of Modified Esters of N-Acyl-N-phenyl-α-amino Acids
Autor: N. D. Chkanikov, V. Yu. Tyutin, A. V. Fokin, A. E. Zelenin, V. D. Sviridov, A. F. Kolomiets
Publikováno v: ChemInform. 25
The C-oxyalkylation of N-aryl-α-amino acids by hexafluoroacetone (1) and methyl trifluoropyruvate (2), followed by acylation of the products3–13, 15, and17 formed, was carried out. The activity of the synthesized anilides against pathogens of plan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2aa49f1dec47ae9468402a394b9d4feb
https://doi.org/10.1002/chin.199419083
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8
The chemistry of perfluoroalkyl-substituted dicyanoethylenes
Autor: N. D. Chkanikov, A. V. Fokin, V. Yu. Tyutin
Publikováno v: Russian Chemical Reviews. 61:766-778
Fundamental data on the means of obtaining and on the reactivity of perfluoroalkyl-substituted dicyanoethylenes are correlated. The principal ways of using these compounds in organic synthesis are shown. Examples are given of the pratical application
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2533156c7d441e908db8f84e5d708b1f
https://doi.org/10.1070/rc1992v061n08abeh000997
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9
Hexafluoroacetone and methyl trifluoropyruvate as precursors of modified esters of N-acyl-N-phenyl-?-amino acids
Autor: N. D. Chkanikov, V. Yu. Tyutin, A. V. Fokin, A. F. Kolomiets, V. D. Sviridov, A. E. Zelenin
Publikováno v: Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:1415-1424
The C-oxyalkylation of N-aryl-α-amino acids by hexafluoroacetone (1) and methyl trifluoropyruvate (2), followed by acylation of the products3–13, 15, and17 formed, was carried out. The activity of the synthesized anilides against pathogens of plan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4c23bf06946c84b62ac9cb5586cde30a
https://doi.org/10.1007/bf00864339
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10
C-alkylation of indoles by 1,1-bis(trifluoromethyl)-2,2-di-cyanoethylene and 2-trifluoromethyl-3,3-dicyanoacrylic acid esters
Autor: A. F. Kolomiets, N. D. Chkanikov, V. Yu. Tyutin, K. V. Komarov, A. V. Fokin
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 40:1070-1073
Indole and its derivatives with various substituants in the 1 and 2 positions of the indole ring react with 1,1-bis(trifluoromethyl)-2,2-dicyanoethylene and 2-trifluoromethyl-3,3-dicyanoacrylic acid esters to give C3-alkylation products.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a67cad2b1432afc3b55e53e4872a7681
https://doi.org/10.1007/bf00961377
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