REACTION OF N-(1-CYANO-1-METHYLETHYL)-ALPHA-PHENYLNITRONE WITH PHENYL-MAGNESIUM, 2-PYRIDYL-MAGNESIUM AND 2-THIENYL-MAGNESIUM BROMIDES - A NEW APPROACH TO ALKYLAROMATIC ALPHA-HYDROXYAMINOKETONES

Authors
KHLESTKIN VK REZNIKOV VA MAZHUKIN DG TIKHONOV AY VOLODARSKY LB
Citation
Vk. Khlestkin et al., REACTION OF N-(1-CYANO-1-METHYLETHYL)-ALPHA-PHENYLNITRONE WITH PHENYL-MAGNESIUM, 2-PYRIDYL-MAGNESIUM AND 2-THIENYL-MAGNESIUM BROMIDES - A NEW APPROACH TO ALKYLAROMATIC ALPHA-HYDROXYAMINOKETONES, Mendeleev communications, (5), 1996, pp. 202-203
Citations number
16
Categorie Soggetti
Chemistry
Journal title
Mendeleev communications → ACNP
ISSN journal
09599436
Issue
5
Year of publication
1996
Pages
202 - 203
Database
ISI
SICI code
0959-9436(1996):5<202:RONWP>2.0.ZU;2-3
Abstract
The reaction of N-(1-cyano-1-methylethyl)-alpha-phenylnitrone with phe nyl-, 2-pyridyl- and 2-thienyl magnesium bromides affords 3-imidazolin es which hydrolyse to alkylaromatic alpha-hydroxyaminoketones, synthon s for stable nitroxides.