Reaction of N-sulfonyl derivatives of 1,4-benzoquinone monoimine with substituted hydrazines
- Авторлар: Konovalova S.A.1, Avdeenko A.P.1, Goncharova S.A.2, D’yakonenko V.V.3, Shishkina S.V.3,4
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Мекемелер:
- Donbass State Engineering Academy
- Sumy State University
- Institute of Single Crystals
- Karazin Kharkiv National University
- Шығарылым: Том 52, № 5 (2016)
- Беттер: 644-649
- Бөлім: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/214272
- DOI: https://doi.org/10.1134/S1070428016050055
- ID: 214272
Дәйексөз келтіру
Аннотация
Reaction direction of N-sulfonyl derivatives of 1,4-benzoquinone monoimine with substituted hydrazines depends on the redox potential of the quinone imine and on the basicity of the hydrazine. Aryl (alkyl)hydrazines of high basicity favor the reduction of quinone monoimine. In reactions with less basic aroylhydrazones N'-(4-oxocyclohexa-2,5-dienylidene)aroylhydrazides were obtained only from the alkylsubstituted in the quinoid ring N-sulfonyl derivatives possessing a lower redox potential.
Авторлар туралы
S. Konovalova
Donbass State Engineering Academy
Email: chimist@dgma.donetsk.ua
Украина, ul. Shkadinova 72, Kramatorsk, 84313
A. Avdeenko
Donbass State Engineering Academy
Хат алмасуға жауапты Автор.
Email: chimist@dgma.donetsk.ua
Украина, ul. Shkadinova 72, Kramatorsk, 84313
S. Goncharova
Sumy State University
Email: chimist@dgma.donetsk.ua
Украина, Sumy
V. D’yakonenko
Institute of Single Crystals
Email: chimist@dgma.donetsk.ua
Украина, Kharkiv
S. Shishkina
Institute of Single Crystals; Karazin Kharkiv National University
Email: chimist@dgma.donetsk.ua
Украина, Kharkiv; Kharkiv
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