Synthesis and structural investigation of 4,4′-dimethyl-[3,3′-bi(1,2,5-oxadiazole)] 5,5′-dioxide

The oxidation of hexane-2,3,4,5-tetraone tetraoxime with dinitrogen tetroxide was studied in different solvents. The primary furoxan ring closure was found to occur involving either two central or two terminal oxime groups to form 4,7-dimethyl[1,2,5]oxadiazolo[3,4-d]pyridazine 1,5,6-trioxide and the previously unknown 4,4′-dimethyl-[3,3′-bi(1,2,5-oxadiazole)] 5,5′-dioxide. The structure of the latter compound was established by X-ray diffraction. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.

Авторы
Obruchnikova N.V.1 , Novikov R.A. 1 , Zlotin S.G.1 , Dorovatovskii P.V. 2 , Khrustalev V.N. 2, 3 , Rakitin O.A.1
Номер выпуска
11
Язык
Английский
Страницы
2044-2048
Статус
Опубликовано
Том
67
Год
2018
Организации
  • 1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., Moscow, 119991, Russian Federation
  • 2 National Research Center “Kurchatov Institute”, 1 ul. Akad. Kurchatova, Moscow, 123182, Russian Federation
  • 3 Peoples’ Friendship University of Russia (RUDN University), 6 ul. Miklukho-Maklaya, Moscow, 117198, Russian Federation
Ключевые слова
2,3,4,5-tetraone tetraoximes; difuroxanyls; dinitrogen tetroxide; oxidation; synthesis
Дата создания
04.02.2019
Дата изменения
04.02.2019
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/36253/
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