Heterocyclization reaction of alpha-imino carbonyl compounds - Derivatives of 2,5-dihydro-1H-imidazole nitroxides

Heterocyclization reaction of alpha-imino carbonyl compounds - Derivatives of 2,5-dihydro-1H-imidazole nitroxides Full article

Journal

European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690

Output data

Year: 2003, Volume: 2003, Number: 22, Pages: 4432-4437 Pages count : DOI: 10.1002/ejoc.200300212

Tags

heterocycles; ketones; luminescence; nitroxides; radiochemistry

Authors

Roshchupkina GA , Pervukhina NV , Rybalova TV , Gatilov YV , Burdukov AB , Reznikov VA

Affiliations

1	(Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
2	(Данные Web of science) Russian Acad Sci, Inst Inorgan Chem, Siberian Div, Novosibirsk 630090, Russia
3	(Данные Web of science) Russian Acad Sci, NN Vorozhtsov Inst Organ Chem, Siberian Div, Novosibirsk 630090, Russia

alpha-Imino carbonyl compounds - derivatives of 3-imidazoline nitroxides - were found to undergo heterocyclization reactions, yielding oxazole and 1,3,5-triazine derivatives. The most probable course of the reaction was suggested by the radioactive label method. The structures of the heterocycles synthesized were verified by X-ray analysis of the mixed-ligand complexes with copper hexafluoroacetylacetonate. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 2003).

Roshchupkina G. , Pervukhina N. , Rybalova T. , Gatilov Y. , Burdukov A. , Reznikov V.
Heterocyclization reaction of alpha-imino carbonyl compounds - Derivatives of 2,5-dihydro-1H-imidazole nitroxides
European Journal of Organic Chemistry. 2003. V.2003. N22. P.4432-4437. DOI: 10.1002/ejoc.200300212 WOS Scopus РИНЦ OpenAlex

Published print:

Nov 1, 2003

Web of science:	WOS:000186735000016
Scopus:	2-s2.0-0344442697
Elibrary:	13439093
OpenAlex:	W2026797925

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Scopus	5
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