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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