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

非对称取代脲的合成与应用
引用本文:薛燕,吴思忠,彭爱东,杨瑛,陆世维.非对称取代脲的合成与应用[J].有机化学,2002,22(8):529-535.
作者姓名:薛燕  吴思忠  彭爱东  杨瑛  陆世维
作者单位:中国科学院大连化学物理研究所国家催化工程技术研究中心,大连,116023
摘    要:总结了合成非对称取代脲的几种方法,分析了各种方法的利弊,介绍了非对称 取代脲的主要应用,指出直接利用一氧化碳进行硒催化的胺与硝基化合物的氧化还 原羰基化反应来合成非对称取代脲的方法是比较有发展前景的方法,并对硒催化的 氧化还原羰基化反应作了较为详细的介绍。

关 键 词:取代    合成  应用    催化  还原  羰基化作用  置换反应  光气
修稿时间:2001年7月2日

Synthesis and application of unsymmetrically substituted ureas
Institution:National Engineering Research Center for Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences,Dalian (116023)
Abstract:Unsymmetrically substituted ureas are widely used in agriculture, medicine and biology. Their main synthetic methods are summarized and analyzed in this article. According to their advantages and disadvantages, it is pointed out that the catalytic method of directly using carbon monoxide is more promising and efficient for the synthesis of unsymmetrical ureas. Combined with our own research work, the substituted reaction of ureas and amines, as well as selenium-catalyzed oxidative carbonylation of amines and reductive carbonylation of nitro compounds with carbon monoxide as a carbonyl reagent are recommended in detail. Through one-step or two-step, unsymmetrical ureas can be obtained easily and conveniently.
Keywords:unsymmetrically substituted urea  selenium catalyst  reductive carbonylation  substituted reaction
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《有机化学》浏览原始摘要信息
点击此处可从《有机化学》下载免费的PDF全文
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