Synthetic Transformations of Sesquiterpene Lactones. 11.* Conjugates Based on Caffeine and Eudesmanolides with N-Containing Linkers Научная публикация
Журнал |
Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388 |
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Вых. Данные | Год: 2020, Том: 56, Номер: 5, Страницы: 855-860 Страниц : 6 DOI: 10.1007/s10600-020-03169-x | ||||
Ключевые слова | caffeine; eudesmanolides; methylenelactones; Michael reaction | ||||
Авторы |
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Организации |
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Реферат:
8-(Aminoalkylamino)caffeine or 8-(piperazinyl)caffeine were formed in high yields by reacting 8-bromo- or 8-chlorocaffeine with linear and cyclic diamines using microwave-assisted organic synthesis. These amines were highly reactive in Michael reactions with sesquiterpene lactones containing active methylene groups. Conjugates with caffeine and eudesmanolide moieties bonded by a N-containing linker were synthesized. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.
Библиографическая ссылка:
Reshetnikov D.V.
, Patrushev S.S.
, Shults E.E.
Synthetic Transformations of Sesquiterpene Lactones. 11.* Conjugates Based on Caffeine and Eudesmanolides with N-Containing Linkers
Chemistry of Natural Compounds. 2020. V.56. N5. P.855-860. DOI: 10.1007/s10600-020-03169-x WOS Scopus РИНЦ
Synthetic Transformations of Sesquiterpene Lactones. 11.* Conjugates Based on Caffeine and Eudesmanolides with N-Containing Linkers
Chemistry of Natural Compounds. 2020. V.56. N5. P.855-860. DOI: 10.1007/s10600-020-03169-x WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 1 сент. 2020 г. |
Опубликована online: | 16 сент. 2020 г. |
Идентификаторы:
Web of science | WOS:000571091800008 |
Scopus | 2-s2.0-85090943791 |
РИНЦ | 45289038 |
OpenAlex | W3088239964 |