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Convenient Synthesis of Indene Derivatives via Intramolecular Friedel-Crafts Cyclization of Tetraaryl Substituted 1,3-Butadienes
作者姓名:孙逊  泉铉治  胡昌奇  林国强
作者单位:[1]Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China [2]Department of Chemistry of Natural Drugs, School of Pharmacy, Fudan University, Shanghai 200032, China
基金项目:Project supported by the National Natural Science Foundation of China (No, 203900506) and the Shanghai Municipal Committee of Science and Technology (Nos, 05JC14057, 054319901),
摘    要:

关 键 词:合成  茚衍生物  分子间环化作用  四芳基取代  1  3-丁二烯  Friedel-Crafts反应  双键转移  刘易斯酸
收稿时间:2005-08-25
修稿时间:2005-08-252005-12-19

Convenient Synthesis of Indene Derivatives via Intramolecular Friedel-Crafts Cyclization of Tetraaryl Substituted 1,3-Butadienes
Sun Xun;Quan XuanZhi;Hu ChangJi;Lin GuoJiang.Convenient Synthesis of Indene Derivatives via Intramolecular Friedel-Crafts Cyclization of Tetraaryl Substituted 1,3-Butadienes[J].Chinese Journal of Chemistry,2006,24(3):430-434.
Authors:Sun Xun;Quan XuanZhi;Hu ChangJi;Lin GuoJiang
Abstract:A convenient and efficient method for the highly regioselecfive synthesis of indene derivatives 4 and 5 from tetraaryl substituted 1,3-butadienes 3 was described. The method involves an intramolecular Friedel-Crafts cyclization and a corresponding double-bond positional shift of isomers 4 and 5 in the presence of different Lewis acids under mild conditions with higher than 90% yields.
Keywords:multiaryl substituted indene derivative  intramolecular cyclization  Friedel-Crafts reaction  doublebond positional shift  Lewis acid
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