Synthesis of 2-aryl(hetaryl)-1-hydroxyimidazoles by the reaction of aliphatic 1,2-hydroxylamino oximes with aromatic and heteroaromatic aldehydes Full article
Journal |
Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171 |
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Output data | Year: 2013, Volume: 62, Number: 5, Pages: 1232-1237 Pages count : DOI: 10.1007/s11172-013-0169-z | ||
Tags | 1-hydroxy-2-aryl(hetaryl)-4,5-dialkylimidazoles; hydroxylamino oximes; aromatic aldehydes; alpha-aryl(hetaryl)nitrones | ||
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Abstract:
A reaction of aliphatic 1,2-hydroxylamino oximes bearing the hydroxylamino group at the secondary carbon atom with aromatic and heteroaromatic aldehydes in acetic acid leads to the corresponding 1-hydroxy-2-aryl(hetaryl)-4,5-dialkylimidazoles in high yields. alpha-Aryl(hetaryl)nitrones initially formed by the condensation of 1,2-hydroxylamino oximes with aldehydes are quantitatively converted to the corresponding imidazoles.
Cite:
Selivanov B.A.
, Tikhonov A.Y.
Synthesis of 2-aryl(hetaryl)-1-hydroxyimidazoles by the reaction of aliphatic 1,2-hydroxylamino oximes with aromatic and heteroaromatic aldehydes
Russian Chemical Bulletin. 2013. V.62. N5. P.1232-1237. DOI: 10.1007/s11172-013-0169-z WOS Scopus РИНЦ
Synthesis of 2-aryl(hetaryl)-1-hydroxyimidazoles by the reaction of aliphatic 1,2-hydroxylamino oximes with aromatic and heteroaromatic aldehydes
Russian Chemical Bulletin. 2013. V.62. N5. P.1232-1237. DOI: 10.1007/s11172-013-0169-z WOS Scopus РИНЦ
ArticleLinkType.TRANSLATED_TO_ORIGINAL:
Селиванов Б.А.
, Тихонов А.Я.
Синтез 2-арил(гетарил)-1-гидроксиимидазолов взаимодействием алифатических 1,2-гидроксил-аминооксимов с ароматическими и гетероароматическими альдегидами
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2013. №5. С.1232. РИНЦ
Синтез 2-арил(гетарил)-1-гидроксиимидазолов взаимодействием алифатических 1,2-гидроксил-аминооксимов с ароматическими и гетероароматическими альдегидами
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2013. №5. С.1232. РИНЦ
Dates:
Published print: | May 1, 2013 |
Published online: | Feb 18, 2014 |
Identifiers:
Web of science | WOS:000332793600014 |
Scopus | 2-s2.0-84894666508 |
Elibrary | 21912781 |
OpenAlex | W2072363937 |