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 |
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Вых. Данные | Год: 1996, Том: 32, Номер: 8, Страницы: 907-913 Страниц : 7 DOI: 10.1007/BF01176965 | ||
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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
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
Даты:
Опубликована в печати: | 1 авг. 1996 г. |
Идентификаторы:
Scopus | 2-s2.0-25444491765 |
РИНЦ | 13232864 |
OpenAlex | W2055219721 |