V. K. Khlestkin, V. A. Reznikov, D. G. Mazhukin, A. Ya. Tikhonov, L. B. Volodarsky, “Reaction of <i>N</i>-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones”, Mendeleev Commun., 1996, Volume 6, Issue 5,Pages <nobr>202

This article is cited in 2 papers

Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones

V. K. Khlestkin, V. A. Reznikov, D. G. Mazhukin, A. Ya. Tikhonov, L. B. Volodarsky

N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: The reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides affords 3-imidazolines which hydrolyse to alkylaromatic α-hydroxyaminoketones, synthons for stable nitroxides.

Language: English

DOI: 10.1070/MC1996v006n05ABEH000646