Reduction of alpha,alpha-dialkoxy-substituted nitroxides: the synthesis ofalpha-alloxynitrones and acetals of N-hydroxyamides

Authors
Bakunova, SM Grigor'ev, IA Kirilyuk, IA Volodarsky, LB
Citation
Sm. Bakunova et al., Reduction of alpha,alpha-dialkoxy-substituted nitroxides: the synthesis ofalpha-alloxynitrones and acetals of N-hydroxyamides, RUSS CHEM B, 48(11), 1999, pp. 2136-2143
Citations number
15
Categorie Soggetti
Chemistry
Journal title
RUSSIAN CHEMICAL BULLETIN
ISSN journal
10665285 → ACNP
Volume
48
Issue
11
Year of publication
1999
Pages
2136 - 2143
Database
ISI
SICI code
1066-5285(199911)48:11<2136:ROANTS>2.0.ZU;2-V
Abstract
Reduction of stable nitroxides derived from tetrahydrooxazole, tetrahydroim idazole, 2,5-dihydroimidazole, and 2,5-dihydroimidazole 3-oxide containing alkoxy groups in alpha-position to the nitroxyl group affords alpha-alkoxyn itrones, acetals of N-hydroxyamides, or their equilibrium mixtures.