Oxidation of dimedone by hydrobromic acid in dimethylsulfoxide and synthesis of 3,5-dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one

M. S. Yusubov, G. A. Zholobova, W. Habicher, V. D. Filimonov

Результат исследований: Материалы для журналаСтатья

Выдержка

Hydrogen bromide in DMSO oxidizes dimedone differently than known cyclic β-diketones: 3,5-dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one are formed instead of vicinal triketones.

Язык оригиналаАнглийский
Страницы (с-по)158-160
Число страниц3
ЖурналRussian Journal of Nondestructive Testing
Том33
Номер выпуска2
СостояниеОпубликовано - фев 1997

Отпечаток

Hydrobromic Acid
hydrobromic acid
Dimethyl Sulfoxide
bromides
Oxidation
Hydrogen
oxidation
Acids
hydrogen
synthesis
cyclopentenone
dimedone

ASJC Scopus subject areas

  • Materials Science (miscellaneous)

Цитировать

Oxidation of dimedone by hydrobromic acid in dimethylsulfoxide and synthesis of 3,5-dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one. / Yusubov, M. S.; Zholobova, G. A.; Habicher, W.; Filimonov, V. D.

В: Russian Journal of Nondestructive Testing, Том 33, № 2, 02.1997, стр. 158-160.

Результат исследований: Материалы для журналаСтатья

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abstract = "Hydrogen bromide in DMSO oxidizes dimedone differently than known cyclic β-diketones: 3,5-dibromo-2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one and 3,5,5-tribromo-4,4-dimethyl-2-hydroxy-2-cyclopenten-1-one are formed instead of vicinal triketones.",
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AU - Zholobova, G. A.

AU - Habicher, W.

AU - Filimonov, V. D.

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