(硫)脲催化剂催化杂原子Michael加成反应的研究进展  

New Advance in Study of Hetero-Michael Reactions Catalyzed by (Thio) Urea

作　　者：王慧[1] 卢楠[1] 

机构地区：[1]山东师范大学化学化工与材料科学学院,山东济南250014

出　　处：《山东化工》2010年第12期21-28,32,共9页Shandong Chemical Industry

基　　金：国家基础研究资助项目(973项目;2007CB936000);国家自然科学基金资助项目(20975064)

摘　　要：(硫)脲催化剂已被证实是一种高效的有机催化剂,被广泛应用于各种Michael加成反应中。关于C-C键生成的Michael加成反应的综述较多,但关于杂原子的Michael加成反应的文章较少。本论文简述了(硫)脲催化剂在杂原子Michael加成反应中的研究新进展。（Thio） urea catalyst has been proved to be an effective organocatalyst. It has been used for the Michael reaction extensively. There were a lot of reviews about Michael reaction of C - C bond formation. However, there was little review about the hetero- Michael reaction. So the hetero- Michael reactions catalyzed by （thio）urea organocatalysts were summarized.

关 键 词：(硫)脲催化剂 杂原子迈克尔加成 有机催化 不对称合成 

分 类 号：O621.251[理学—有机化学]