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Preparation of 2-unsubstituted 5-aryl(hetaryl)-1-hydroxy-1H-imidazoles from of 4-aryl(hetaryl)-1-hydroxy-2,5-dihydro-1H-imidazole-2-carboxylic acid 3-oxides Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2023, Volume: 59, Number: 11-12, Pages: 752-757 Pages count : 6 DOI: 10.1007/s10593-024-03268-5
Tags glyoxylic acid hydroxyaminooximes 1-hydroxy-2,5-dihydro-1H-imidazole 3-oxides 1-hydroxy-1H-imidazoles
Authors Nikolaenkova Elena B. 1 , Grishchenko Stanislav Yu. 1 , Rybalova Tatyana V. 1 , Tikhonov Alexei Ya. 1
Affiliations
1 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences

Abstract: Alkylaromatic 1-hydroxyamino-2-oximes reacted at the hydroxyamino group with glyoxylic acid hydrate, providing 4-aryl(hetaryl)-1-hydroxy-2,5-dihydro-1H-imidazole-2-carboxylic acid 3-oxides that were converted upon heating into 5-aryl(hetaryl)-1-hydroxy-1H-imidazoles containing a hydrogen atom at the heterocycle position 2.
Cite: Nikolaenkova E.B. , Grishchenko S.Y. , Rybalova T.V. , Tikhonov A.Y.
Preparation of 2-unsubstituted 5-aryl(hetaryl)-1-hydroxy-1H-imidazoles from of 4-aryl(hetaryl)-1-hydroxy-2,5-dihydro-1H-imidazole-2-carboxylic acid 3-oxides
Chemistry of Heterocyclic Compounds. 2023. V.59. N11-12. P.752-757. DOI: 10.1007/s10593-024-03268-5 WOS РИНЦ OpenAlex
Dates:
Submitted: Apr 18, 2023
Accepted: Sep 19, 2023
Identifiers:
Web of science: WOS:001138394700002
Elibrary: 65147488
OpenAlex: W4390779666
Citing:
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Web of science 1
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