4-(Nitroalkyl- and dinitroalkyl-ONN-azoxy)-3-cyanofuroxans and some of their derivatives


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Abstract

Dibromoisocyanurate-mediated reaction of 4-amino-3-cyanofuroxans with pseudonitroles of aliphatic, alicyclic, and heterocyclic series (including pseudonitroles bearing ethylcarboxyl or additional nitro group) resulted in 4-(nitroalkyl- and dinitroalkyl-ONN-azoxy)-3-cyanofuroxans. Subsequent chemical transformations gave 4-(1,3-dinitrooxy-2-nitropropyl-2-ONN-azoxy)-3-cyano- and 4-carbamoylfuroxans, as well as 4-(1,1-dinitroethyl-ONN-azoxy)-3-(1H-tetrazol-5-yl)furoxans.

About the authors

V. V. Parakhin

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Author for correspondence.
Email: Parakhin@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

N. I. Shlykova

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: Parakhin@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

O. A. Luk´yanov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: Parakhin@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991


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