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 Научная публикация

Журнал

Mendeleev Communications
ISSN: 0959-9436

Вых. Данные

Год: 1996, Том: 6, Номер: 5, Страницы: 202-203 Страниц : 2 DOI: 10.1070/MC1996v006n05ABEH000646

Авторы

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

Организации

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

Опубликована в печати:

1 янв. 1996 г.

Scopus	2-s2.0-25044480548
РИНЦ	13249517
OpenAlex	W2951455027