Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process

Reaction of arylglyoxal oximes ArCOCH=NOH (Ar = 4-MeOC6H4, Ph) with 5-arylfurazanopyrazines proceeds as vicarious nucleophilic substitution of hydrogen in pyrazine ring with the elimination of hyponitrous acid, affording 5-(aroylmethylidene)-6-aryl-4H-furazano[3,4-b]pyrazines. Structure of the product was confirmed by X-ray diffraction. © 2019

Authors
Tsyganov D.V.1 , Samet A.V.1 , Dorovatovskii P.V. 2 , Khrustalev V.N. 2, 3 , Semenov V.V.1
Publisher
Royal Society of Chemistry
Number of issue
3
Language
English
Pages
296-298
Status
Published
Volume
29
Year
2019
Organizations
  • 1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991, Russian Federation
  • 2 National Research Center ‘Kurchatov Institute’, Moscow, 123182, Russian Federation
  • 3 Peoples Friendship University of Russia (RUDN University), Moscow, 117198, Russian Federation
Date of creation
19.07.2019
Date of change
19.07.2019
Short link
https://repository.rudn.ru/en/records/article/record/38657/
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