Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/51497
Title: Synthesis of nitroxyl radical by direct nucleophilic functionalization of a C-H bond in the azadiene systems
Authors: Varaksin, M. V.
Tretyakov, E. V.
Utepova, I. A.
Romanenko, G. V.
Bogomyakov, A. S.
Stass, D. V.
Sagdeev, R. Z.
Ovcharenko, V. I.
Chupakhin, O. N.
Issue Date: 2012
Citation: Synthesis of nitroxyl radical by direct nucleophilic functionalization of a C-H bond in the azadiene systems / M. V. Varaksin, E. V. Tretyakov, I. A. Utepova, G. V. Romanenko, A. S. Bogomyakov, D. V. Stass, R. Z. Sagdeev, V. I. Ovcharenko, O. N. Chupakhin // Russian Chemical Bulletin. — 2012. — Vol. 61. — № 7. — P. 1469-1473.
Abstract: Cyclic dinitrones underwent nucleophilic substitution of the hydrogen atom in the reaction with a paramagnetic carbanion, the lithium derivative of 4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, to give polyfunctional nitronyl nitroxyls. © 2012 Springer Science+Business Media New York.
Keywords: ESR SPECTRA
NITRONES
NITRONYL NITROXYLS
REACTION OF NUCLEOPHILIC SUBSTITUTION OF HYDROGEN
URI: http://elar.urfu.ru/handle/10995/51497
Access: info:eu-repo/semantics/openAccess
SCOPUS ID: 84887357499
WOS ID: 000321771700017
PURE ID: 1079693
ISSN: 1066-5285
DOI: 10.1007/s11172-012-0190-7
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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