Вид документа : Статья из журнала Шифр издания : Г/C 73 Автор(ы) : Savchuk M. I., Kopchuk D. S., Egorov I. N., Khasanov A. F., Rybakova S. S., Zyryanov G. V., Rusinov V. L., Chupakhin O. N. Заглавие : Combination of the Snh/aza-diels–alder reactions as effective synthetic approach to 8-hydroxy(methoxy)-substituted 2-[6-(1-methylindol-3-yl)pyridin-2-yl]quinoline ligands/fluorophores Место публикации : Russian Journal of General Chemistry. - 2021. - Vol. 91, № 5. - С. 779-784 ББК : Г Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ Ключевые слова (''Своб.индексиров.''): aza-diels–alder reaction--1,2,4-triazines--8-methoxyquinoline--demethylation--autoclave Аннотация: 8-Hydroxy(methoxy)-substituted 2-[6-(1-methylindol-3-yl)pyridin-2-yl]quinoline ligands were synthesized by means of combination of SNH reaction between 8-methoxy-substituted 2-(6-aryl-1,2,4-triazin-3-yl)quinolones and indole and aza-Diels–Alder reaction of the obtained 1,2,4-triazines with 2,5-norbornadiene. The demethylation of quinoline moiety of 1,2,4-triazine precursor during aza-Diels–Alder reaction in autoclave was demonstrated. Доп.точки доступа: Savchuk, M. I.; Kopchuk, D. S.; Egorov, I. N.; Khasanov, A. F.; Rybakova, S. S.; Zyryanov, G. V.; Rusinov, V. L.; Chupakhin, O. N.