Zobrazeno 1 - 10
of 25
pro vyhledávání: '"N I, Sheludchenko"'
Autor:
L. I. Mazaletskaya, N. I. Sheludchenko, L. N. Shishkina, I. Yu. Chukicheva, E. V. Buravlev, O. V. Shchukina, A. V. Kutchin
Publikováno v:
Russian Journal of Physical Chemistry A. 96:964-968
Autor:
L. N. Shishkina, V. O. Shvydkiy, A. Yu. Povkh, L. I. Mazaletskaya, N. I. Sheludchenko, M. V. Kozlov
Publikováno v:
Russian Journal of Physical Chemistry B. 14:498-503
Model systems were proposed, using previously obtained experimental data, for investigating the mechanism of regulation of oxidative processes in lipids isolated from natural objects, preparations, and various components of aqueous medium. The models
Publikováno v:
Russian Chemical Bulletin. 68:1919-1923
An inhibition by the semisynthetic polyphenols bearing bicyclic isobornyl substituents and OH groups arranged variously relative to each other was investigated in the presence of lecithin. A decreased efficiency of the inhibition by the phenolic anti
Publikováno v:
Russian Journal of General Chemistry. 88:1635-1640
Tetra(meso-aryl)porphyrins containing 2,6-dimethoxyphenol unit distant from the macrocycle and adjacent to it have been prepared. Radical scavenging activity of the obtained compounds has been estimated in the model reaction of ethylbenzene oxidation
Autor:
Dmitry V. Belykh, Oksana G. Shevchenko, L. I. Mazaletskaya, T. K. Rocheva, N. I. Sheludchenko
Publikováno v:
Macroheterocycles. 11:95-102
Autor:
L. I. Mazaletskaya, Natalya V. Khrustova, Mikhail V. Kozlov, N. I. Sheludchenko, Lyudmila Shishkina
Publikováno v:
Antioxidants in Systems of Varying Complexity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11a090b7b91450baefd78727c4988948
https://doi.org/10.1201/9780429325168-2
https://doi.org/10.1201/9780429325168-2
Autor:
L. I. Mazaletskaya, Evgeny V. Buravlev, N. I. Sheludchenko, Dmitrii V. Belykh, Olga V Shchukina, I. S. Khudyaeva, Irina Yu. Chukicheva, T. K. Rocheva
Publikováno v:
Molecules, Vol 23, Iss 7, p 1718 (2018)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
This article focuses on the antiradical activity of a number of 2,6-diisobornylphenol-porphyrin conjugates with various spacers between the porphyrin and phenolic fragments in the model reaction of ethylbenzene oxidation initiated by azoisobutyric ac
Autor:
Evgeny V. Buravlev, N. I. Sheludchenko, I. Yu. Chukicheva, L. I. Mazaletskaya, I. S. Khudyaeva, Dmitry V. Belykh
Publikováno v:
Macroheterocycles. 8:371-375
Autor:
L. N. Shishkina, Evgeny V. Buravlev, L. I. Mazaletskaya, K. M. Marakulina, A. V. Kutchin, Yu. K. Lukanina, I. G. Plashchina, Irina V. Fedorova, N. I. Sheludchenko, I. Yu. Chukicheva
Publikováno v:
Russian Chemical Bulletin. 63:2007-2012
The rate constants were measured for the reactions of isobornyl phenols (IBPs) containing methyl and tert-butyl substituents in the ortho-position with peroxide radicals in the initiated oxidation of ethylbenzene. The IR spectra of IBPs were analyzed
Publikováno v:
Petroleum Chemistry. 54:309-315
The inhibition activity of chlorophyll a derivatives with different substituents on the macrocycle and their Zn(II) and Co(II) chelates has been studied in the model reaction of ethylbenzene oxidation. It has been found that the values of the inducti