Search Results - "Buravlev, E V"

Experimental Evaluation of the Effectiveness of Isobornylphenols in the Model of Pathospermia and Their Effect on the Antioxidant—Prooxidant Balance of Male Germ Cells by Borovskaya, T. G., Vychuzhanina, A. V., Shchemerova, Yu. A., Buravlev, E. V., Chukicheva, I. Yu, Kuchin, A. V.

“…We studied the effect of antioxidants dibornol (2,6-diisobornyl-4-methylphenol) and its derivative (4-hydroxymethyl-2,6-diisobornylphenol), members of the…”
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Revised data for the reaction of benzyltrimethylammonium tribromide with sterically hindered p-cresols by Buravlev, E. V.

“…2,6-Di- tert -butyl-4-methylphenol reacted with an equimolar amount of benzyltrimethylammonium tribromide to give 4-bromomethyl derivative but not…”
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Synthesis and Antioxidant Properties of Hydroxycinnamic Acid Derivatives Containing Isobornyl Substituents by Dvornikova, I. A., Buravlev, E. V., Fedorova, I. V., Shevchenko, O. G., Chukicheva, I. Yu, Kuchin, A. V.

“…New hydroxycinnamic acid derivatives were synthesized by reacting malonic acid and 4-hydroxybenzaldehydes with isobornyl and/or alkyl substituents. The…”
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Antioxidant activity of Mannich bases derived from natural and synthetic phenols by Shevchenko, O. G., Buravlev, E. V.

“…The data obtained earlier on the Mannich bases derived from natural and synthetic phenols are summarized, the structure—antioxidant activity relationship is…”
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Synthesis and evaluation of the antioxidant activity of amino derivatives of o-isobornylphenols by Buravlev, E. V., Shevchenko, O. G.

“…The reaction of o -isobornylphenols with bismuth( iii ) nitrate provided o - and p -nitrophenols, the reduction of the nitro group of which with zinc dust in…”
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Synthesis and antioxidant properties of N-substituted aminomethyl derivatives of 2-isobornylphenol by Buravlev, E. V., Shevchenko, O. G.

“…A series of 2-isobornylphenol derivatives containing aminomethyl groups either at ortho -(monoderivatives) or ortho - and para -positions (bis-derivatives)…”
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Synthesis and comparative evaluation of the antioxidant activity for some new derivatives of 2,6-diisobornylphenol bearing an aminomethyl group at the position 4 by Buravlev, E. V., Shevchenko, O. G., Kutchin, A. V.

“…New derivatives of 2,6-diisobornylphenol containing (phenylamino)methyl or (benzylamino)methyl moiety, or heterocyclic (1 H -benzo[ d ]imidazol-1-yl)methyl,…”
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Synthesis and evaluation of the antioxidant properties for some novel aminomethyl derivatives of 2,6-diisobornylphenol bearing a pinane moiety by Dvornikova, I. A., Buravlev, E. V., Shevchenko, O. G., Chukicheva, I. Yu, Kutchin, A. V.

“…Some new derivatives based on 2,6-diisobornylphenol and containing amine moieties of the pinane structure at the para -position relative to the phenolic…”
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2-Hydroxy-3-isobornyl-5-methylbenzaldehyde derivatives: synthesis and antioxidant activity in vitro by Buravlev, E. V., Shevchenko, O. G.

“…A series of N - and O-containing derivatives based on 2-hydroxy-3-isobornyl-5-methylbenzaldehyde was synthesized. A comparative evaluation of their radical…”
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Comparative evaluation of antioxidant activity of 2-alkyl-4-methylphenols and their 6-n-octylaminomethyl derivatives by Buravlev, E. V., Fedorova, I. V., Shevchenko, O. G.

“…A series of 2-alkyl-4-methyl-6- n -octylaminomethylphenols (where alkyl is methyl or tert -butyl group, or terpene substituent) was synthesized. A comparative…”
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Synthesis and antioxidant properties of some N- and O-containing 2-isobornyl-6-methylphenol derivatives by Buravlev, E. V., Fedorova, I. V., Shevchenko, O. G., Kutchin, A. V.

“…A series of 2-isobornyl-6-methylphenol derivatives bearing either hydroxymethyl, aminomethyl, or N -acetylaminomethyl group at the para -position with respect…”
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Synthesis and antioxidant properties of benzimidazole derivatives with isobornylphenol fragments by Dvornikova, I. A., Buravlev, E. V., Fedorova, I. V., Shevchenko, O. G., Chukicheva, I. Yu, Kutchin, A. V.

“…A series of new 2-substituted-1 H -benzimidazoles was synthesized on the basis of 4-hydroxybenzaldehydes. Their antioxidant properties were evaluated in the in…”
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Evaluation of antiviral activity of terpenophenols and some of their N- and O-derivatives by Chukicheva, I. Yu, Buravlev, E. V., Dvornikova, I. A., Fedorova, I. V., Zarubaev, V. V., Slita, A. V., Esaulkova, Ya. L., Kutchin, A. V.

“…A comparative evaluation of the antiviral activity of a number of new and previously synthesized terpenophenols and their N - or O -containing derivatives…”
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Comparative evaluation of the antioxidant activity of some ortho-substituted mono- and dialkylphenols with the para-positioned hydroxymethyl group by Buravlev, E. V., Fedorova, I. V., Shevchenko, O. G., Kutchin, A. V.

“…The para -hydroxymethyl derivatives of 2,6-di- tert -butylphenol, 2,6-diisobornylphenol, 2-isobornyl-6- tert -butylphenol, 2-isobornyl-6-methylphenol, and…”
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Synthesis and membrane-protective activity of 2,6-diisobornylphenol derivatives with N- and O-containing fragments at position 4 by Buravlev, E. V., Chukicheva, I. Yu, Shevchenko, O. G., Kutchin, A. V.

“…Two series of new amide derivatives containing 2,6-diisobornylphenol moiety were synthesized based on 3,5-diisobornyl-4-hydroxybenzoic acid and…”
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Effect of the Nature of a Substitute in a Molecule of Isobornylphenol on Its Reactivity by Mazaletskaya, L. I., Sheludchenko, N. I., Shishkina, L. N., Chukicheva, I. Yu, Buravlev, E. V., Shchukina, O. V., Kutchin, A. V.

“…Reaction rate constants ( k 7 ) are measured for bis- and sulfur-containing isobornylphenols (IBPs) with peroxide radicals of ethylbenzene. The antioxidant…”
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Structure—hemolytic activity relationship in isobornylphenol derivatives by Shevchenko, O. G., Plyusnina, S. N., Buravlev, E. V., Chukicheva, I. Yu, Fedorova, I. V., Shchukina, O. V., Kutchin, A. V.

“…A structure — hemolytic activity relationship in isobornylphenol derivatives was analysed. The morphological transformation of erythrocytes under the influence…”
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Composition and properties of the reaction products of p-cresol with camphene by Chukicheva, I. Yu, Buravlev, E. V., Dvornikova, I. A., Fedorova, I. V., Chernysheva, G. A., Aliev, O. I., Smol’yakova, V. I., Anishchenko, A. M., Sidekhmenova, A. V., Plotnikov, M. B., Kutchin, A. V.

“…The products of the reaction between p -cresol and camphene were isolated and characterized. Their antiradical activity and toxicity were studied. The…”
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Synthesis and membrane-protective activity of 4-aminomethyl derivatives of 2,6-diisobornylphenol by Buravlev, E. V., Chukicheva, I. Yu, Shevchenko, O. G., Suponitskii, K. Yu, Kutchin, A. V.

“…A series of 4-aminomethyl derivatives of 2,6-diisobornylphenol containing tertiary and secondary amino groups were synthesized. Their toxicity and the…”
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Asymmetrically substituted tetra(meso-aryl)porphyrins bearing peripheral 2,6-diisobornylphenol and 2,6-di-tert-butylphenol moieties by Belykh, D. V., Rocheva, T. K., Buravlev, E. V., Chukicheva, I. Yu, Kutchin, A. V.

“…Asymmetrically substituted tetra( meso -aryl)porphyrins bearing peripheral diisobornyl- phenol and di- tert -butylphenol moieties were synthesized by a mixed…”
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