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学科主题: 天然产物有机化学
题名: 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
作者: Huang YM(黄有铭); Zheng CW(郑昌武); Zhao G(赵刚)
通讯作者: 赵刚
刊名: J. Org. Chem.
发表日期: 2015
DOI: 10.1021/jo502904n
卷: 80, 期:8, 页:3798-3805
收录类别: SCI
文章类型: 论文
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.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000353315000008
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/39784
Appears in Collections:中科院天然产物有机化学重点实验室_期刊论文

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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

Recommended Citation:
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.
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