4-(Nitroalkyl- and dinitroalkyl-ONN-azoxy)-3-cyanofuroxans and some of their derivatives
- Authors: Parakhin V.V.1, Shlykova N.I.1, Luk´yanov O.A.1
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Affiliations:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Issue: Vol 66, No 2 (2017)
- Pages: 320-326
- Section: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/240033
- DOI: https://doi.org/10.1007/s11172-017-1734-7
- ID: 240033
Cite item
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