Title of article
A convenient synthesis of quinolines by reactions of o-isocyano-β-methoxystyrenes with nucleophiles
Author/Authors
Kazuhiro Kobayashi، نويسنده , , Keiichi Yoneda، نويسنده , , Kazuna Miyamoto، نويسنده , , Osamu Morikawa، نويسنده , , Hisatoshi Konishi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
7
From page
11639
To page
11645
Abstract
2,4-Disubstituted quinolines have been synthesized by reactions of o-isocyano-β-methoxystyrenes, which can be easily prepared from commercially available o-aminophenyl ketones in three steps, with alkyl(or aryl)lithiums in generally good yields. Subsequently, o-isocyano-β-methoxystyrenes have also proved to react efficiently with lithium dialkylamides to afford the corresponding 4-substituted N,N-dialkylquinolin-2-amines in satisfactory yields.
Keywords
organolithium , Quinoline , Styrene , isocyanide , lithium amide
Journal title
Tetrahedron
Serial Year
2004
Journal title
Tetrahedron
Record number
1087382
Link To Document