Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XV. Synthesis and bromination of 4-(cinnamoyloxyimino)-cyclohexa-2,5-dienones
- Авторы: Konovalova S.A.1, Avdeenko A.P.1, Goncharova S.A.2
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Учреждения:
- Donbass State Engineering Academy
- Sumy State University
- Выпуск: Том 52, № 7 (2016)
- Страницы: 939-945
- Раздел: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/214651
- DOI: https://doi.org/10.1134/S1070428016070034
- ID: 214651
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Аннотация
New 4-(cinnamoyloxyimino)cyclohexa-2,5-dien-1-ones were synthesized, and their bromination afforded bromine addition products to the syn- and anti-C=C bonds of the quinoid ring. In all cases, bromine addition to the C=C double bond of the cinnamoyl fragment was observed.
Об авторах
S. Konovalova
Donbass State Engineering Academy
Email: chimist@dgma.donetsk.ua
Украина, ul. Shkadinova 72, Kramatorsk, 84313
A. Avdeenko
Donbass State Engineering Academy
Автор, ответственный за переписку.
Email: chimist@dgma.donetsk.ua
Украина, ul. Shkadinova 72, Kramatorsk, 84313
S. Goncharova
Sumy State University
Email: chimist@dgma.donetsk.ua
Украина, ul. Rimskogo-Korsakova 2, Sumy, 40007
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