Zobrazeno 1 - 10
of 22
pro vyhledávání: '"I. A. Dvornikova"'
Autor:
I. Yu. Chukicheva, E. V. Buravlev, I. A. Dvornikova, I. V. Fedorova, V. V. Zarubaev, A. V. Slita, Ya. L. Esaulkova, A. V. Kutchin
Publikováno v:
Russian Chemical Bulletin. 71:2473-2481
Publikováno v:
Russian Chemical Bulletin. 70:2185-2188
Autor:
I. Yu. Chukicheva, Evgeny V. Buravlev, A. V. Kuchin, Irina V. Fedorova, I. A. Dvornikova, Oksana G. Shevchenko
Publikováno v:
Chemistry of Natural Compounds. 55:658-664
New hydroxycinnamic acid derivatives were synthesized by reacting malonic acid and 4-hydroxybenzaldehydes with isobornyl and/or alkyl substituents. The antiradical, antioxidant, and membrane-protective activities were assessed in various in vitro mod
Autor:
A. V. Kutchin, I. Yu. Chukicheva, Evgeny V. Buravlev, Oksana G. Shevchenko, Irina V. Fedorova, I. A. Dvornikova
Publikováno v:
Russian Chemical Bulletin. 68:1000-1005
A series of new 2-substituted-1H-benzimidazoles was synthesized on the basis of 4-hydroxybenzaldehydes. Their antioxidant properties were evaluated in the in vitro models and compared with those of known analogs. The structural specifi c features of
Autor:
Galina A. Chernysheva, Anna M. Anishchenko, Evgeny V. Buravlev, Oleg I. Aliev, A. V. Sidekhmenova, V. I. Smol’yakova, Mark B. Plotnikov, A. V. Kutchin, Irina V. Fedorova, I. A. Dvornikova, I. Yu. Chukicheva
Publikováno v:
Russian Chemical Bulletin. 68:993-999
The products of the reaction between p-cresol and camphene were isolated and characterized. Their antiradical activity and toxicity were studied. The pharmacological activity of the most active stereoisomer of 2,6-diisobornyl-4-methyl phenol in rats
Publikováno v:
Inorganica Chimica Acta. 477:300-305
Seven novel palladium complexes of the type [Pd(HL)Cl2] and [Pd(L)Cl] containing chiral pinane ligands (HL = 3-[(2-aminoethyl)imino]-pinane-2-ol; 3,3′-(ethylenediimino)bis-pinane-2-ol; cis-3-(2-aminoethylamino)-pinane-2-ol; cis-3,3′(ethylenediami
Publikováno v:
Chemistry & Biodiversity. 16
A series of novel esters and amides was synthesized on the basis of para-coumaric acid containing isobornyl groups in ortho-positions relative to the phenolic hydroxy group. Antioxidant properties of the obtained compounds were evaluated and compared
Publikováno v:
Russian Journal of Organic Chemistry. 51:480-492
Chiral diamines with C 1 and C 2 symmetry have been synthesized from 2-hydroxypinan-3-one and tested as ligands in Cu-catalyzed asymmetric nitroaldol reaction of nitromethane with 4-nitrobenzaldehyde.
Publikováno v:
Russian Journal of Organic Chemistry. 48:938-942
New 2,6-diisobornylphenol derivatives having formyl, hydroxymethyl, and carboxy groups in the para position with respect to the hydroxy group were synthesized. 4-Hydroxy-3,5-diisobornylbenzoic acid was obtained in a moderate yield through intermediat
Autor:
Evgeny V. Buravlev, Yu. V. Nelyubina, A. V. Kuchin, I. Yu. Chukicheva, I. A. Dvornikova, Larisa L. Frolova
Publikováno v:
Russian Journal of Organic Chemistry. 47:1130-1138
New nitrogen-containing chiral ligands were synthesized containing terpene fragments of pinane and camphane structure.