REACTION OF SEVERAL RESVERATROL GLYCOSIDE DERIVATIVES WITH HYPOCHLORITES IN VARIOUS MEDIA Научная публикация
| Журнал |
Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388 |
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| Вых. Данные | Год: 2012, Том: 48, Номер: 1, Страницы: 1-7 Страниц : DOI: 10.1007/s10600-012-0146-z | ||||
| Ключевые слова | resveratrol; stilbene glycosides; oxidation; hypochlorites; triphenylmethyl ethers; TEMPO | ||||
| Авторы |
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| Организации |
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Реферат:
The reactions of pterostilbenoside (trans-3,5-dimethoxystilben-4'-O-beta-D-glucoside) and Ar-O-Tr derivatives of resveratroloside (3,5-dihydroxystilben-4'-O-beta-D-glucoside) and pinostilbenoside (3-methoxy-5-hydroxystilben-4'-O-beta-D-glucoside) with NaOCl and t-BuOCl in the presence of the stable nitroxyl radical TEMPO were studied in various media. It was found that the principal product of pterostilbenoside transformation was its 2,6-dichloroderivative, a part of which was oxidized to form 2,6-dichloropterostilbene glucuronide. Trityl ethers of resveratroloside and pinostilbenoside reacted with the hypochlorites to form mixtures of products.
Библиографическая ссылка:
Rogachev A.D.
, Komarova N.I.
, Pozdeeva A.V.
, Korchagina D.V.
, Vasil'ev V.G.
, Salakhutdinov N.F.
, Tolstikov G.A.
REACTION OF SEVERAL RESVERATROL GLYCOSIDE DERIVATIVES WITH HYPOCHLORITES IN VARIOUS MEDIA
Chemistry of Natural Compounds. 2012. V.48. N1. P.1-7. DOI: 10.1007/s10600-012-0146-z WOS Scopus РИНЦ OpenAlex
REACTION OF SEVERAL RESVERATROL GLYCOSIDE DERIVATIVES WITH HYPOCHLORITES IN VARIOUS MEDIA
Chemistry of Natural Compounds. 2012. V.48. N1. P.1-7. DOI: 10.1007/s10600-012-0146-z WOS Scopus РИНЦ OpenAlex
Даты:
| Опубликована в печати: | 1 мар. 2012 г. |
| Опубликована online: | 21 мар. 2012 г. |
Идентификаторы БД:
| Web of science: | WOS:000302243100001 |
| Scopus: | 2-s2.0-84858318611 |
| РИНЦ: | 17980325 |
| OpenAlex: | W2077024478 |