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

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 OpenAlex
Dates:
Published print: Jul 1, 2004
Identifiers:
Web of science: WOS:000222521900007
Scopus: 2-s2.0-2942590957
Elibrary: 13468506
OpenAlex: W2072660507
Citing:
DB Citing
Web of science 19
Scopus 16
Elibrary 16
OpenAlex 15
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