New Synthetic Method and Antioxidant Activity of Betulin Diformate and Allobetulin Formate

書目詳細資料
Parent link:Chemistry of Natural Compounds
Vol. 55, iss. 6.— 2019.— [P. 1094-1097]
Corporate Authors: Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение химической инженерии, Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
其他作者: Arrous S. Salah, Boudebouz I. Imene, Parunov I., Plotnikov E. V. Evgeny Vladimirovich, Voronova O. A. Olesya Aleksandrovna
總結:Title screen
A simple and effective method for formylation of betulin using formic acid and 3a,6a-diphenylthioglycoluril is reported. The yield of betulin diformate was 87%. Allobetulin formate (95%) was prepared by reacting betulin diformate with trifluoroacetic acid. The structures of betulin diformate and allobetulin formate were confirmed by IR and NMR spectroscopy. The antioxidant activity of the synthesized compounds was studied.
Режим доступа: по договору с организацией-держателем ресурса
語言:英语
出版: 2019
主題:
在線閱讀:https://doi.org/10.1007/s10600-019-02902-5
格式: 電子 Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663290
實物特徵
總結:Title screen
A simple and effective method for formylation of betulin using formic acid and 3a,6a-diphenylthioglycoluril is reported. The yield of betulin diformate was 87%. Allobetulin formate (95%) was prepared by reacting betulin diformate with trifluoroacetic acid. The structures of betulin diformate and allobetulin formate were confirmed by IR and NMR spectroscopy. The antioxidant activity of the synthesized compounds was studied.
Режим доступа: по договору с организацией-держателем ресурса
DOI:10.1007/s10600-019-02902-5