Aminonitrone-N-hydroxyaminoimine tautomeric equilibrium in the series of 1-hydroxy-2-imidazolines

Aminonitrone-N-hydroxyaminoimine tautomeric equilibrium in the series of 1-hydroxy-2-imidazolines Научная публикация

Журнал

Journal of Molecular Structure
ISSN: 0022-2860 , E-ISSN: 1872-8014

Вых. Данные

Год: 2004, Том: 697, Номер: 1-3, Страницы: 49-60 Страниц : DOI: 10.1016/j.molstruc.2004.02.028

Ключевые слова

tautomerism; ab initio calculations; 2-imidazoline; 4,5-Dihydro-1H-imidazole; nitrone

Авторы

Popov SA , Andreev RV , Romanenko GV , Ovcharenko VI , Reznikov VA

Организации

1	(Данные Web of science) Russian Acad Sci, NN Vorozhtsov Inst Organ Chem, Siberian Branch, Novosibirsk, Russia
2	(Данные Web of science) Russian Acad Sci, Int Tomog Ctr, Siberian Branch, Novosibirsk, Russia

A series of 2-substituted 1-hydroxy-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazoles have been synthesized. Various effects on the state of the aminonitrone-N-hydroxyaminoimine tautomeric equilibrium, including solvent effects and substituent effect in the 2 position of heterocycle, have been studied. (C) 2004 Elsevier B.V. All rights reserved.

Popov S. , Andreev R. , Romanenko G. , Ovcharenko V. , Reznikov V.
Aminonitrone-N-hydroxyaminoimine tautomeric equilibrium in the series of 1-hydroxy-2-imidazolines
Journal of Molecular Structure. 2004. V.697. N1-3. P.49-60. DOI: 10.1016/j.molstruc.2004.02.028 WOS Scopus РИНЦ

Опубликована в печати:

1 июл. 2004 г.

Web of science	WOS:000222521900007
Scopus	2-s2.0-2942590957
РИНЦ	13468506
OpenAlex	W2072660507