Reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- And 2-thienyl magnesium bromides: A new approach to alkylaromatic α-hydroxyaminoketones

Reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- And 2-thienyl magnesium bromides: A new approach to alkylaromatic α-hydroxyaminoketones Full article

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 1996, Volume: 6, Number: 5, Pages: 202-203 Pages count : 2 DOI: 10.1070/MC1996v006n05ABEH000646

Authors

Khlestkin V.K. ¹ , Reznikov V.A. ¹ , Mazhukin D.G. ¹ , Tikhonov A.Ya. ¹ , Volodarsky L.B. ¹

Affiliations

1	Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

The reaction of N-(1-cyano-1-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.

Khlestkin V.K. , Reznikov V.A. , Mazhukin D.G. , Tikhonov A.Y. , Volodarsky L.B.
Reaction of N-(1-cyano-1-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- And 2-thienyl magnesium bromides: A new approach to alkylaromatic α-hydroxyaminoketones
Mendeleev Communications. 1996. V.6. N5. P.202-203. DOI: 10.1070/MC1996v006n05ABEH000646 Scopus РИНЦ

Published print:

Jan 1, 1996

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