首页 | 本学科首页   官方微博 | 高级检索  
     


A convenient synthesis of quinolines by reactions of o-isocyano-β-methoxystyrenes with nucleophiles
Authors:Kazuhiro Kobayashi  Keiichi Yoneda  Kazuna Miyamoto  Osamu Morikawa  Hisatoshi Konishi
Affiliation:Department of Materials Science, Faculty of Engineering, Tottori University, Koyama-minami, Tottori 680-8552, Japan
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:Isocyanide   Lithium amide   Organolithium   Quinoline   Styrene
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号