查耳酮衍生物与丙二酸二酯的不对称迈克尔加成反应研究  

Research of asymmetric Michael addition reaction of chalcone derivatives with malonate ester

作　　者：贾永兵 张睿[1] 谢彬[1] 陈国术[1] 刘天穗[1] 陈亿新[1] 

机构地区：[1]广州大学化学化工学院,广东广州510006

出　　处：《广州大学学报（自然科学版）》2014年第3期47-51,共5页Journal of Guangzhou University:Natural Science Edition

基　　金：国家自然科学基金资助项目(21072036)

摘　　要：查尔酮或带有查尔酮片段的衍生物具有抗炎症、抗细菌、除草等功效.以(R)-ALB为催化剂,叔丁醇钾作碱源,通过不对称迈克尔加成反应合成了一系列具有光学活性查耳酮片段的1,5-二羰基化合物,并且取得了良好的产率和极高的对映选择性.反应收率最高可达84%,反应的对映选择性最高可达98%.Some chalcones and their analogues showed excellent biological activities , such as antibacterial , an-tiviral, antifungal, antitumor activities and inhibiting the growth of weed .Herein a series of 1, 5-dicarbonyl compounds were synthesized from the asymmetric Michael addition reaction between chalcone derivatives and es -ter with （ R）-ALB complex as catalyst and then got better yield and highly enantioselective .The corresponding adducts were obtained in up to 84%and 98%ee.

关 键 词：查耳酮 不对称迈克尔加成反应 (R)-ALB 1 5-二羰基化合物 

分 类 号：O632[理学—高分子化学]