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 Научная публикация

Журнал

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

Вых. Данные

Год: 2003, Том: 2003, Номер: 22, Страницы: 4432-4437 Страниц : DOI: 10.1002/ejoc.200300212

Ключевые слова

heterocycles; ketones; luminescence; nitroxides; radiochemistry

Авторы

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

Организации

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

Опубликована в печати:

1 нояб. 2003 г.

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

БД	Цитирований
Web of science	4
Scopus	5
РИНЦ	5
OpenAlex	5