New synthetic approach to epoxyisoindolo[2,1-a]quinolines based on cycloaddition reactions of 2-furyl-substituted tetrahydroquinolines with maleic anhydride and acryloyl chloride

A procedure was developed for the synthesis of hydrogenated furyl-substituted furo[3,2-c]quinolines, pyrano[3,2-c]quinolines, and 4-ethoxy-and 4-(2-oxopyrrolidin-1-yl)quinolines. The reactions of these compounds with acryloyl chloride and maleic anhydride produce epoxyisoindolo[2,1-a]quinoline derivatives through successive acylation at the quinoline nitrogen atom and intramolecular exo-[4+2]-cycloaddition at the furan moiety. © 2007 Springer Science+Business Media, Inc.

Авторы
Zubkov F.I. 1 , Zaitsev V.P. 1 , Peregudov A.S.2 , Mikhailova N.M. 1 , Varlamov A.V. 1
Номер выпуска
5
Язык
Английский
Страницы
1063-1079
Статус
Опубликовано
Том
56
Год
2007
Организации
  • 1 Peoples' Friendship University of Russia, 6 ul. Miklukho-Maklaya, Moscow 117198, Russian Federation
  • 2 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, Moscow 119991, Russian Federation
Ключевые слова
Furfurylamines; Intramolecular Diels-Alder reaction; Isoindolo[2,1-a]quinolines; Povarov reaction; Tetrahydroquinolines
Дата создания
19.10.2018
Дата изменения
13.08.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/3243/
Поделиться

Другие записи