Standard

Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols. / Vlasov, P.S.; Sergeeva, O.Yu.; Domnina, N.S.; Chukicheva, I.Yu.; Buravlev, E.V.; Kuchin, A.V.

In: Chemistry of Natural Compounds, Vol. 48, No. 4, 2012, p. 531-534.

Research output: Contribution to journal › Article

Harvard

Vlasov, PS, Sergeeva, OY, Domnina, NS, Chukicheva, IY, Buravlev, EV & Kuchin, AV 2012, 'Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols', Chemistry of Natural Compounds, vol. 48, no. 4, pp. 531-534. https://doi.org/10.1007/s10600-012-0302-5

APA

Vlasov, P. S., Sergeeva, O. Y., Domnina, N. S., Chukicheva, I. Y., Buravlev, E. V., & Kuchin, A. V. (2012). Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols. Chemistry of Natural Compounds, 48(4), 531-534. https://doi.org/10.1007/s10600-012-0302-5

Vancouver

Vlasov PS, Sergeeva OY, Domnina NS, Chukicheva IY, Buravlev EV, Kuchin AV. Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols. Chemistry of Natural Compounds. 2012;48(4):531-534. https://doi.org/10.1007/s10600-012-0302-5

Author

Vlasov, P.S. ; Sergeeva, O.Yu. ; Domnina, N.S. ; Chukicheva, I.Yu. ; Buravlev, E.V. ; Kuchin, A.V. / Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols. In: Chemistry of Natural Compounds. 2012 ; Vol. 48, No. 4. pp. 531-534.

BibTeX

@article{ecf8bf5f9a7f4cb68aba80c75bdaeca5,
title = "Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols",
abstract = "New macromolecular antioxidants that were conjugates of dextran or hydroxyethylated starch with functionalized derivatives synthesized from 2,6-diisobornyl-4-methylphenol were prepared. Their antiradical activity compared with derivatives of 2,6-di-tert-butyl-4-methylphenol was studied in a model reaction with 2,2-diphenyl-1-picrylhydrazyl. The studied conjugates exhibited greater activity than sterically hindered phenols not bonded to a polymer chain. The synthesized isobornyl derivatives were more active than previously studied tert-butyl analogs.",
keywords = "2, 6-diisobornyl-4-methylphenol – terpenoids – dextran – hydroxyethylated starch – antioxidants – 2, 2-diphenyl-1-picrylhydrazyl",
author = "P.S. Vlasov and O.Yu. Sergeeva and N.S. Domnina and I.Yu. Chukicheva and E.V. Buravlev and A.V. Kuchin",
year = "2012",
doi = "10.1007/s10600-012-0302-5",
language = "English",
volume = "48",
pages = "531--534",
journal = "Chemistry of Natural Compounds",
issn = "0009-3130",
publisher = "Springer Nature",
number = "4",

}

RIS

TY - JOUR

T1 - Synthesis and properties of macromolecular esters of carboxy-substituted derivatives of hindered phenols

AU - Vlasov, P.S.

AU - Sergeeva, O.Yu.

AU - Domnina, N.S.

AU - Chukicheva, I.Yu.

AU - Buravlev, E.V.

AU - Kuchin, A.V.

PY - 2012

Y1 - 2012

N2 - New macromolecular antioxidants that were conjugates of dextran or hydroxyethylated starch with functionalized derivatives synthesized from 2,6-diisobornyl-4-methylphenol were prepared. Their antiradical activity compared with derivatives of 2,6-di-tert-butyl-4-methylphenol was studied in a model reaction with 2,2-diphenyl-1-picrylhydrazyl. The studied conjugates exhibited greater activity than sterically hindered phenols not bonded to a polymer chain. The synthesized isobornyl derivatives were more active than previously studied tert-butyl analogs.

AB - New macromolecular antioxidants that were conjugates of dextran or hydroxyethylated starch with functionalized derivatives synthesized from 2,6-diisobornyl-4-methylphenol were prepared. Their antiradical activity compared with derivatives of 2,6-di-tert-butyl-4-methylphenol was studied in a model reaction with 2,2-diphenyl-1-picrylhydrazyl. The studied conjugates exhibited greater activity than sterically hindered phenols not bonded to a polymer chain. The synthesized isobornyl derivatives were more active than previously studied tert-butyl analogs.

KW - 2

KW - 6-diisobornyl-4-methylphenol – terpenoids – dextran – hydroxyethylated starch – antioxidants – 2

KW - 2-diphenyl-1-picrylhydrazyl

U2 - 10.1007/s10600-012-0302-5

DO - 10.1007/s10600-012-0302-5

M3 - Article

VL - 48

SP - 531

EP - 534

JO - Chemistry of Natural Compounds

JF - Chemistry of Natural Compounds

SN - 0009-3130

IS - 4

ER -

ID: 5351968