Sciact
  • EN
  • RU

Synthesis of berberine bromide analogs containing tertiary amides of acetic acid in the 9-O-position Научная публикация

Журнал Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Вых. Данные Год: 2013, Том: 48, Номер: 6, Страницы: 1047-1053 Страниц : DOI: 10.1007/s10600-013-0461-z
Ключевые слова berberine; berberine chloride; berberrubine; tertiary amides; isoquinoline alkaloids; hypocholesterolemic activity
Авторы Nechepurenko I. V. 1 , Komarova N. I. 1 , Vasil'ev V. G. 1 , Salakhutdinov N. F. 1
Организации
1 (Данные Web of science) Russian Acad Sci, N N Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Реферат: 9-O-Acetamide analogs of berberine bromide were prepared in 20-87% yields via reaction of the isoquinoline alkaloid berberrubine with tertiary amides of bromoacetic acid. Aminolysis did not occur during reaction of methyl-2-(9-demethoxyberberine bromide-9-yl)hydroxyacetate with secondary amines. The corresponding acid or its ethyl ester was isolated.
Библиографическая ссылка: Nechepurenko I.V. , Komarova N.I. , Vasil'ev V.G. , Salakhutdinov N.F.
Synthesis of berberine bromide analogs containing tertiary amides of acetic acid in the 9-O-position
Chemistry of Natural Compounds. 2013. V.48. N6. P.1047-1053. DOI: 10.1007/s10600-013-0461-z WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 янв. 2013 г.
Опубликована online: 22 февр. 2013 г.
Идентификаторы БД:
Web of science: WOS:000315417600033
Scopus: 2-s2.0-84874403842
РИНЦ: 24941697
OpenAlex: W1967868005
Цитирование в БД:
БД Цитирований
Web of science 8
Scopus 9
РИНЦ 8
OpenAlex 9
Альметрики: