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This article is cited in 2 scientific papers (total 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.
Citation:
V. K. Khlestkin, V. A. Reznikov, D. G. Mazhukin, A. Ya. Tikhonov, L. B. Volodarsky, “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”, Mendeleev Commun., 6:5 (1996), 202–203
Linking options:
https://www.mathnet.ru/eng/mendc4980 https://www.mathnet.ru/eng/mendc/v6/i5/p202
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