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

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

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1996, Volume: 32, Number: 8, Pages: 907-913 Pages count : 7 DOI: 10.1007/BF01176965

Authors

Samsonov V.A. ¹ , Volodarskii L.B. ¹ , Bagryanskaya I.Yu. ¹ , Gatilov Yu.V. ¹

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Section, Russian Academy of Sciences (SO RAN), Novosibirsk 630090, Russian Federation

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.

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

Published print:

Aug 1, 1996

Scopus	2-s2.0-25444491765
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