中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones

文献类型:期刊论文

作者Huang YM(黄有铭); Zheng CW(郑昌武); Zhao G(赵刚)
刊名J. Org. Chem.
出版日期2015
卷号80期号:8页码:3798-3805
其他题名Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones
通讯作者赵刚
英文摘要Enantioselective Robinson-type annulation reaction between beta-ketoamide and alpha,beta-unsaturated ketone was developed by utilizing the amino acid derived primary secondary diamine catalysts. The less reactive acyclic beta-ketoamides employed as both electrophile and nucleophile are reported in this asymmetric tandem reaction. A number of chiral cyclohexenone derivatives containing an amide group were obtained in high yields and good selectivities.
学科主题天然产物有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/jo502904n
语种英语
WOS记录号WOS:000353315000008
源URL[http://ir.sioc.ac.cn/handle/331003/39784]  
专题上海有机化学研究所_中科院天然产物有机化学重点实验室
作者单位中科院上海有机化学研究所, 天然产物有机合成化学重点实验室
推荐引用方式
GB/T 7714
Huang YM,Zheng CW,Zhao G. Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones[J]. J. Org. Chem.,2015,80(8):3798-3805.
APA 黄有铭,郑昌武,&赵刚.(2015).Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones.J. Org. Chem.,80(8),3798-3805.
MLA 黄有铭,et al."Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones".J. Org. Chem. 80.8(2015):3798-3805.

入库方式: OAI收割

来源:上海有机化学研究所

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