155126-86-6Relevant academic research and scientific papers
Stable Nitroxides With Hydrogen At α-Carbon of the Nitroxyl Group
Reznikov, Vladimir A.,Volodarsky, Leonid B.
, p. 2239 - 2240 (1994)
The reactions of 1-hydroxy-3-imidazoline-3-oxides containing hydrogen in the 2-position with PhLi or PhMgBr lead to acyclic α-hydroxylaminooximes.The oxidation of the latter gives stable acyclic nitroxides with hydrogen at the α-carbon atom.
Stable nitroxyl radicals with a hydrogen atom at α-carbon atom of nitroxyl group
Reznikov,Gutorov,Gatilov,Rybalova,Volodarsky
, p. 384 - 392 (2007/10/03)
Nitroxyl radicals containing the diphenylmethyl group as one of the substituents at the nitroxyl group are stable compounds that can be isolated in an individual state. N-(2-Hydroxy-3-methyl-2-phenylcyclohexyl)-N-diphenylmethylnitroxyl was characterized b
Interaction of Heterocyclic Nitrones With Organometallic Reagents As a Method For the Synthesis of New Types of Nitroxides
Reznikov, Vladimir A.,Volodarsky, Leonid B.
, p. 10669 - 10692 (2007/10/02)
The reactions of heterocyclic nitroxides: 3-imidazoline-3-oxides, 2H- (4H)-imidazole mono- and dioxides, dihydropyrazine-1,4-dioxides, with organometallic reagents and subsequent oxidation led to heterocyclic nitroxides of 3-(2)-imidazoline and 3-(2)-imidazoline-3-oxide, dihydropyrazine oxide, monocyclic imidazolidine biradicals and stable acyclic nitroxides with hydrogen at the α-carbon atom.
