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Heteroannelations with pinane-derived ß-enaminoaldehyde Научная публикация

Журнал Heterocyclic Communications
ISSN: 0793-0283
Вых. Данные Год: 2000, Том: 6, Номер: 4, Страницы: 327-332 Страниц : 6
Авторы Popov S.A. 1 , Tkachev A.V. 1
Организации
1 (Scopus) Department of Natural Sciences, Novosibirsk State University, Novosibirsk Inst. of Organ. Chem., Academician Lavrentjev Ave. 9, Novosibirsk, 630090, Russian Federation

Реферат: Synthesis of new chiral fused pyridines and pyrimidines with pinane carbon frame prospective as bioactive compounds is described. Heterocylisations of pinane-derived ß-enaminoaldehyde, need generally more rigid conditions than for o-aminobenzaldehyde, probably, both due to sterical and electronic reasons.
Библиографическая ссылка: Popov S.A. , Tkachev A.V.
Heteroannelations with pinane-derived ß-enaminoaldehyde
Heterocyclic Communications. 2000. V.6. N4. P.327-332. WOS Scopus РИНЦ
Идентификаторы БД:
Web of science: WOS:000090119700008
Scopus: 2-s2.0-0034366619
РИНЦ: 13354549
Цитирование в БД:
БД Цитирований
Scopus 2
Web of science 2
РИНЦ 3