Zobrazeno 1 - 8
of 8
pro vyhledávání: '"V. V. Tolstyakov"'
Autor:
O. O. Gololobova, V. V. Tolstyakova
Publikováno v:
Людина і довкілля: Проблеми неоекології, Iss 29 (2018)
Studies are devoted to the ecological assessment of the pond aquatic ecosystem components, Bobrivka village, Kharkiv district, Kharkiv oblast. Purpose. In order to achieve the goal, it was tasked to determine the seasonal redistribution of hydrochemi
Externí odkaz:
https://doaj.org/article/f9723a9f4ccf4b38b1e55a81afa12cbe
Publikováno v:
Russian Journal of General Chemistry. 91:72-76
A series of new 6-phosphonylated 1H-imidazo[2,1-c][1,2,4]triazoles was synthesized by the reaction of diethyl chloroethynylphosphonate with 2-substituted 3-amino-1,2,4-triazoles followed by 5-endo-dig cyclization. It was found that 3-amino-5-bromo-1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03c105f3c3ab9b93ca46e1714e22e0a9
https://doi.org/10.1134/s1070363221010072
https://doi.org/10.1134/s1070363221010072
Autor:
Aleksandra V. Protas, V. V. Tolstyakov, S. S. Chuprun, E. A. Popova, O. S. Zarubina, Rostislav E. Trifonov, E. S. Tolstobrova
Publikováno v:
Russian Journal of Organic Chemistry. 52:1681-1685
New tetrazolyl derivatives of L- and D-phenylalanine were synthesized by azidation of n-propyl esters of (2S)- and (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-aminophenyl)propionic acids and by a series of subsequent chemical transformation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8da232bf8a4a6b815d14949812802a3b
https://doi.org/10.1134/s1070428016110221
https://doi.org/10.1134/s1070428016110221
Publikováno v:
Russian Chemical Bulletin. 58:2356-2361
A method for the preparation of new 3-nitro-1,2,4-triazole derivatives has been suggested based on modification of the N-hydroxymethyl group by nitration and nucleophilic substitution reactions. Thermal stability of 3-nitro-1,2,4-triazole N-nitroxy-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf9762d35b958c84bda8591d536477f5
https://doi.org/10.1007/s11172-009-0327-5
https://doi.org/10.1007/s11172-009-0327-5
Publikováno v:
Russian Journal of General Chemistry. 77:2179-2185
The use of hydrazine as reagent in nucleophilic substitution and reduction in the 1,2,4-triazole series in combination with introduction of labile protecting groups makes it possible to synthesize 5-hydrazino-3-nitro-1H-1,2,4-triazole and 3-chloro-5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12478ed3cb867bff508e895caec0b254
https://doi.org/10.1134/s107036320712016x
https://doi.org/10.1134/s107036320712016x
Autor:
V. V. Tolstyakov, I. V. Tselinskii
Publikováno v:
Russian Journal of General Chemistry. 74:399-404
A diphenylmethyl protective group is suggested for use in the synthesis of 5-R-3-nitro-1H-1,2,4-triazoles unsubstituted at the cyclic nitrogen atom, via nucleophilic substitution of 5-bromo- and 5-methylsulfonyl groups.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c28f3c4d13a37543a3dc1bfd34e3192
https://doi.org/10.1023/b:rugc.0000030397.19585.ec
https://doi.org/10.1023/b:rugc.0000030397.19585.ec
Publikováno v:
ChemInform. 42
The novel title compounds are synthesized with medium yields starting from N-hydroxymethyltriazole derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04ec4bf21a869852453a05123962fbad
https://doi.org/10.1002/chin.201107166
https://doi.org/10.1002/chin.201107166
Autor:
M. S. Pevzner, V. V. Tolstyakov
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3067bdcdc6f5db8ad6c6e4d335ecb568
https://doi.org/10.1002/chin.199835173
https://doi.org/10.1002/chin.199835173