Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yu. V. Yushkova"'
Publikováno v:
Chemistry of Natural Compounds. 53:1059-1065
Covalent, ionic, and ionic-covalent conjugates of trolox and α-tocopherol with 1-aminoadamantane were synthesized. Their structures were elucidated using mass spectrometry and IR, PMR, and 13C NMR spectroscopy. The water solubility of the ionic trol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::438ea4c2b76be45bb91a7171c391a324
https://doi.org/10.1007/s10600-017-2201-2
https://doi.org/10.1007/s10600-017-2201-2
Publikováno v:
Chemistry of Natural Compounds. 52:1015-1019
Six ionic conjugates with nitroxyl radical amino-TEMPO and diethanolamine as the amines were synthesized from trolox and α-tocopherol succinates. The water solubility of the synthesized ammonium salts was determined. It was shown that formation of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0605090a9c7a078224a5bc36ac74782a
https://doi.org/10.1007/s10600-016-1850-x
https://doi.org/10.1007/s10600-016-1850-x
Autor:
Vyacheslav V. Martemyanov, E. I. Chernyak, Yu. V. Yushkova, S. O. Nikolenko, S. V. Morozov, Sergey V. Pavlushin
Publikováno v:
Chemistry of Natural Compounds. 52:193-198
The individual group compositions of hydroxycinnamic acid derivatives, flavonoids, terpenoids, fatty acids, and hydrocarbons from Betula pendula leaves during early leaf development were studied using GC-MS and HPLC. The contents of biologically acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d017667e123ec8ec712860f59f005f6
https://doi.org/10.1007/s10600-016-1592-9
https://doi.org/10.1007/s10600-016-1592-9
Publikováno v:
Chemistry of Natural Compounds. 53:764-766
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::523f19161b7118f1e42bf37c97162b5e
https://doi.org/10.1007/s10600-017-2115-z
https://doi.org/10.1007/s10600-017-2115-z
Publikováno v:
Chemistry of Natural Compounds. 51:1070-1073
Three types of trolox dimers (bis-trolox derivatives), two of which were pairs of trolox molecules bound symmetrically through an ethylenediamine linker with covalent or ionic bonds and one of which was an asymmetric ionic–covalent conjugate, were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08206824398a74064537b74deabb1023
https://doi.org/10.1007/s10600-015-1494-2
https://doi.org/10.1007/s10600-015-1494-2
Publikováno v:
Chemistry of Natural Compounds. 50:827-831
Spin-labeled α-tocopherol succinyl derivatives were synthesized by the reaction of α-tocopherol succinate with 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl, 3-aminomethyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl, and 3-amino-2,2,5,5-tetramethylpyrroli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::638837a224a9b852870dc9d44eeefcad
https://doi.org/10.1007/s10600-014-1093-7
https://doi.org/10.1007/s10600-014-1093-7
Autor:
Yu. F. Polienko, Igor A. Grigor'ev, S. V. Morozov, Yu. V. Gatilov, E. I. Chernyak, Yu. V. Yushkova
Publikováno v:
Chemistry of Natural Compounds. 49:253-257
Reaction of 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox) with 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl, 3-amino-2,2,5,5-tetramethylpyrrolidine-1-oxyl, and 3-aminomethyl-2,2,5,5-tetramethylpyrrolidine-1-oxyl synthesized the corr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c62688a2049e83d465a2f57eba07814
https://doi.org/10.1007/s10600-013-0574-4
https://doi.org/10.1007/s10600-013-0574-4
Autor:
E. I. Chernyak, Yu. V. Yushkova, S. V. Pavlushin, S. O. Nikolenko, V. V. Martemyanov, S. V. Morozov
Publikováno v:
Chemistry of Natural Compounds. 52:1161-1161
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0f2b78a22437621fddc6ff83a5c0bee
https://doi.org/10.1007/s10600-016-1896-9
https://doi.org/10.1007/s10600-016-1896-9