An efficient synthesis of isoindolo[2,1-a]quinoline derivatives via imino Diels-Alder and intramolecular Diels-Alder reactions with furan

The straightforward synthesis of new isoindolo[2,1-a]quinoline derivatives from 2,4-disubstituted 1,2,3,4-tetrahydroquinolines bearing a furan fragment via the intramolecular Diels-Alder reaction is reported. The synthesis of key precursors was realized with excellent levels of diastereoselectivity either by Povarov reaction or by a multicomponent condensation approach. © Georg Thieme Verlag Stuttgart.

Авторы
Kouznetsov V.V.1 , Cruz U.M.1 , Zubkov F.I. 2 , Nikitina E.V. 2
Журнал
Номер выпуска
3
Язык
Английский
Страницы
375-384
Статус
Опубликовано
Год
2007
Организации
  • 1 Laboratorio de Química Orgánica Y Biomolecular, CIBIMOL, Universidad Industrial de Santander, A.A. 678, Bucaramanga, Colombia
  • 2 Organic Chemistry Department, Russian Peoples Friendship University, 6 Miklukho-Maklayia St, Moscow, 117198, Russian Federation
Ключевые слова
Furans; Intramolecular Diels-Alder reaction; Isoindolo[2,1-a]quinolines; Povarov reaction; Quinolines
Дата создания
19.10.2018
Дата изменения
13.08.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/3274/
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