BEHAVIOR OF 1-HYDROXY-2,2,5,5-TETRAMETHYL-3-IMIDAZOLINE-3-OXIDE AND THE CORRESPONDING NITROXYL RADICALS IN SUPERACID MEDIA

BEHAVIOR OF 1-HYDROXY-2,2,5,5-TETRAMETHYL-3-IMIDAZOLINE-3-OXIDE AND THE CORRESPONDING NITROXYL RADICALS IN SUPERACID MEDIA Научная публикация

Журнал

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230

Вых. Данные

Год: 1991, Том: 40, Номер: 12, Страницы: 2399-2404 Страниц : 6 DOI: 10.1007/BF00959709

Авторы

Morozov S.V. ¹ , Volodarskii L.B. ¹ , Shubin V.G. ¹

Организации

1	Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, USSR

The protonation of 1-R-2,2,5,5-tetramethyl-3-imidazoline-3-oxides (R = OH, O) in superacid media was investigated with H-1 and C-13 NMR. The hydroxylamino dication forming on protonation can undergo imidazoline ring opening to form an isomeric mixture of diprotonated N-(2-hydroxyimino-1,1-dimethylethyl), alpha, alpha-dimethylnitrones.

Morozov S.V. , Volodarskii L.B. , Shubin V.G.
BEHAVIOR OF 1-HYDROXY-2,2,5,5-TETRAMETHYL-3-IMIDAZOLINE-3-OXIDE AND THE CORRESPONDING NITROXYL RADICALS IN SUPERACID MEDIA
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1991. V.40. N12. P.2399-2404. DOI: 10.1007/BF00959709 WOS Scopus РИНЦ

Опубликована в печати:

1 дек. 1991 г.

Web of science	WOS:A1991JH55200010
Scopus	2-s2.0-34249915843
РИНЦ	30975909
OpenAlex	W2080989006