Synthesis and Properties of Functional Derivatives of 2,6-Diisobornylphenol and 2-Isobornyl-6-(1-phenylethyl)phenol
- Авторы: Shchukina O.1, Chukicheva I.1, Shevchenko O.2, Kolegova T.1, Suponitsky K.3, Kutchin A.1
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Учреждения:
- Institute of Chemistry, Komi Scientific Centre, Ural Branch, Russian
- Institute of Biology, Komi Science Center, Ural Branch
- A.N. Nesmeyanov Institute of Organoelement Compounds
- Выпуск: Том 88, № 4 (2018)
- Страницы: 664-675
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222126
- DOI: https://doi.org/10.1134/S1070363218040096
- ID: 222126
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Аннотация
New isobornylphenol derivatives have been produced by introducing allyl, hydroxypropyl, and chloropropyl groups into the para-position of 2,6-diisobornylphenol and 2-isobornyl-6-(1-phenylethyl)phenol. The radical scavenging and antioxidant activity and the membrane-protective properties of the newly-obtained compounds in chemical and biological model systems were studied.
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Об авторах
O. Shchukina
Institute of Chemistry, Komi Scientific Centre, Ural Branch, Russian
Email: chukichevaiy@mail.ru
Россия, ul. Pervomayskaya 48, Syktyvkar, Komi Republic, 167000
I. Chukicheva
Institute of Chemistry, Komi Scientific Centre, Ural Branch, Russian
Автор, ответственный за переписку.
Email: chukichevaiy@mail.ru
Россия, ul. Pervomayskaya 48, Syktyvkar, Komi Republic, 167000
O. Shevchenko
Institute of Biology, Komi Science Center, Ural Branch
Email: chukichevaiy@mail.ru
Россия, Syktyvkar
T. Kolegova
Institute of Chemistry, Komi Scientific Centre, Ural Branch, Russian
Email: chukichevaiy@mail.ru
Россия, ul. Pervomayskaya 48, Syktyvkar, Komi Republic, 167000
K. Suponitsky
A.N. Nesmeyanov Institute of Organoelement Compounds
Email: chukichevaiy@mail.ru
Россия, Moscow
A. Kutchin
Institute of Chemistry, Komi Scientific Centre, Ural Branch, Russian
Email: chukichevaiy@mail.ru
Россия, ul. Pervomayskaya 48, Syktyvkar, Komi Republic, 167000