104406-67-9Relevant academic research and scientific papers
ROUTE THE STABLE NITROXIDES WITH ALKOXY GROUPS AT α-CARBON-THE DERIVTIVES OF 2- AND 3-IMIDAZOLINES
Grigor'ev, I. A.,Volodarsky, L. B.,Starichenko, V. F.,Shchukin, G. I.,Kirilyuk, I. A.
, p. 5085 - 5088 (2007/10/02)
Oxidation of 1-hydroxy-5,5-dimethyl-3-imidazoline-3-oxides containing one or two hydrogen atoms in position 2 of the heterocycle with lead dioxide in alcohol leads to stable nitroxides with alkoxy groups at α-carbon, the derivatives of 2- and 3-imidazolines, via the intermediate formation of 4H-imidazol-1,3-dioxides.
