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Formation of the pyrroline-N-oxide ring by the reaction of isonitrosoketones with enamines and some conversions of the pyrroline-N-oxides obtained Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1996, Том: 32, Номер: 8, Страницы: 907-913 Страниц : 7 DOI: 10.1007/BF01176965
Авторы Samsonov V.A. 1 , Volodarskii L.B. 1 , Bagryanskaya I.Yu. 1 , Gatilov Yu.V. 1
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Section, Russian Academy of Sciences (SO RAN), Novosibirsk 630090, Russian Federation

Реферат: Compounds containing the pyrroline-N-oxide ring are obtained when isonitrosoketones - 2,6-dihydroxyiminocyclohexanone and ω-isonitrosoacetophenone - react with enamines. The compounds obtained behave as synthetic equivalents of 1,4-dicarbonyl compounds when undergoing reaction with amines, hydrazine, and hydroxylamine. ©1997 Plenum Publishing Corporation.
Библиографическая ссылка: Samsonov V.A. , Volodarskii L.B. , Bagryanskaya I.Y. , Gatilov Y.V.
Formation of the pyrroline-N-oxide ring by the reaction of isonitrosoketones with enamines and some conversions of the pyrroline-N-oxides obtained
Chemistry of Heterocyclic Compounds. 1996. V.32. N8. P.907-913. DOI: 10.1007/BF01176965 Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 авг. 1996 г.
Идентификаторы БД:
Scopus: 2-s2.0-25444491765
РИНЦ: 13232864
OpenAlex: W2055219721
Цитирование в БД:
БД Цитирований
Scopus 3
OpenAlex 1
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