Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones
其他题名Asymmetric Robinson-Type Annulation Reaction between beta-Ketoamides and alpha,beta-Unsaturated Ketones
Huang YM(黄有铭); Zheng CW(郑昌武); Zhao G(赵刚)
2015
发表期刊J. Org. Chem.
卷号80期号:8页码:3798-3805
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.
文章类型论文
学科领域天然产物有机化学
DOI10.1021/jo502904n
URL查看原文
收录类别SCI
语种英语
WOS记录号WOS:000353315000008
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文献类型期刊论文
条目标识符http://ir.sioc.ac.cn/handle/331003/39784
专题中科院天然产物有机化学重点实验室
通讯作者Zhao G(赵刚)
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
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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.
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