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.

Authors
Zubkov F.I. 1 , Zaitsev V.P. 1 , Peregudov A.S.2 , Mikhailova N.M. 1 , Varlamov A.V. 1
Number of issue
5
Language
English
Pages
1063-1079
Status
Published
Volume
56
Year
2007
Organizations
  • 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
Keywords
Furfurylamines; Intramolecular Diels-Alder reaction; Isoindolo[2,1-a]quinolines; Povarov reaction; Tetrahydroquinolines
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