Aminonitrone-N-hydroxyaminoimine tautomeric equilibrium in the series of 1-hydroxy-2-imidazolines Full article
Journal |
Journal of Molecular Structure
ISSN: 0022-2860 , E-ISSN: 1872-8014 |
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Output data | Year: 2004, Volume: 697, Number: 1-3, Pages: 49-60 Pages count : DOI: 10.1016/j.molstruc.2004.02.028 | ||||
Tags | tautomerism; ab initio calculations; 2-imidazoline; 4,5-Dihydro-1H-imidazole; nitrone | ||||
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Abstract:
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.
Cite:
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
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
Dates:
Published print: | Jul 1, 2004 |
Identifiers:
Web of science | WOS:000222521900007 |
Scopus | 2-s2.0-2942590957 |
Elibrary | 13468506 |
OpenAlex | W2072660507 |