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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

Реферат: 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.
Библиографическая ссылка: 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 OpenAlex
Даты:
Опубликована в печати: 1 янв. 1996 г.
Идентификаторы БД:
Scopus: 2-s2.0-25044480548
РИНЦ: 13249517
OpenAlex: W2951455027
Цитирование в БД:
БД Цитирований
Scopus 1
РИНЦ 1
OpenAlex 1
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