首页 | 本学科首页   官方微博 | 高级检索  
     检索      

以森田-贝里斯-希尔曼(MBH)碳酸酯为原料合成多取代1,4-二氢喹啉类衍生物
引用本文:史鸿燕,钟莹,赵志刚.以森田-贝里斯-希尔曼(MBH)碳酸酯为原料合成多取代1,4-二氢喹啉类衍生物[J].有机化学,2021(2):677-687.
作者姓名:史鸿燕  钟莹  赵志刚
作者单位:西南民族大学化学与环境保护工程学院
基金项目:西南民族大学中央高校基本科研业务费专项资金(No.2018NQN35)资助项目.
摘    要:以森田-贝里斯-希尔曼(MBH)碳酸酯和活泼亚甲基类化合物为原料,在叔胺的催化下,经历两次亲核取代反应得到关键叠氮中间体,再与三苯基膦作用经连续的Staudinger反应、分子内aza-Wittig反应及异构化等,在温和的反应条件下合成了17个新的多取代1,4-二氢喹啉类衍生物.中间体及目标化合物均为新化合物,其结构均...

关 键 词:1  4-二氢喹啉  氮杂Wittig反应  MBH碳酸酯  叠氮化物

Synthesis of Multi-substituted 1,4-Dihydroquinoline Derivatives from Morita-Baylis-Hillman(MBH)Carbonates
Shi Hongyan,Zhong Ying,Zhao Zhigang.Synthesis of Multi-substituted 1,4-Dihydroquinoline Derivatives from Morita-Baylis-Hillman(MBH)Carbonates[J].Chinese Journal of Organic Chemistry,2021(2):677-687.
Authors:Shi Hongyan  Zhong Ying  Zhao Zhigang
Institution:(College of Chemistry&Environment Protection Engineering,Southwest Minzu Universily,Chengdu 610041)
Abstract:Using Morita-Baylis-Hillman(MBH) carbonates and active methylene compounds as raw materials, the key azide intermediates were obtained through two nucleophilic substitution reactions catalyzed by tertiary amine. Then, seventeen new multi-substituted 1,4-dihydroquinoline derivatives were obtained by sequential Staudinger/intramolecular aza-Wittig/isomerization reactions of the azide intermediates with triphenylphosphine under mild conditions. The intermediates and target compounds are all new compounds, and their structures have been confirmed by IR, HRMS, 1H NMR and 13C NMR techniques.
Keywords:1  4-dihydroquinolines  aza-Wittig reaction  Morita-Baylis-Hillman(MBH)carbonate  azide
本文献已被 维普 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