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Synthesis and analgesic activity of pyrrolidinomorphinan derivatives Научная публикация

Журнал Pharmaceutical Chemistry Journal
ISSN: 1573-9031
Вых. Данные Год: 2007, Том: 41, Номер: 2, Страницы: 74-77 Страниц : 4 DOI: 10.1007/s11094-007-0016-3
Авторы Shul'ts E.E. 1 , Tolstikova T.G. 1 , Tolstikov S.E. 1 , Daibova V.T. 1 , Shakirov M.M. 1 , Bolkunov A.V. 1 , Dolgikh M.P. 1
Организации
1 Vorozhtsov Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk, Russia

Реферат: Diels– Alder reactions of (-)-thebaine with N-substituted maleimides have been used to obtain cycloadducts possessing-facial stereoselectivity. The 3-O- and 6-O-demethylated derivatives as well as the products of complete and partial reduction of carbonyl groups in the pyrrolidinedione moiety were also obtained. Some of the synthesized compounds have proved to be promising analgesics. The introduction of the bromine atom into the aryl moiety favors prolongation of the analgesic effect.
Библиографическая ссылка: Shul'ts E.E. , Tolstikova T.G. , Tolstikov S.E. , Daibova V.T. , Shakirov M.M. , Bolkunov A.V. , Dolgikh M.P.
Synthesis and analgesic activity of pyrrolidinomorphinan derivatives
Pharmaceutical Chemistry Journal. 2007. V.41. N2. P.74-77. DOI: 10.1007/s11094-007-0016-3 Scopus
Даты:
Поступила в редакцию: 5 сент. 2005 г.
Опубликована в печати: 1 февр. 2007 г.
Идентификаторы БД:
Scopus: 2-s2.0-34548575044
Цитирование в БД:
БД Цитирований
Scopus 4
Альметрики: