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
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Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353 |
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| Output data | Year: 1996, Volume: 32, Number: 8, Pages: 907-913 Pages count : 7 DOI: 10.1007/BF01176965 | ||
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Abstract:
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.
Cite:
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
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
Dates:
| Published print: | Aug 1, 1996 |
Identifiers:
| Scopus: | 2-s2.0-25444491765 |
| Elibrary: | 13232864 |
| OpenAlex: | W2055219721 |