中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to beta,gamma-Unsaturated alpha-Keto Esters

文献类型:期刊论文

作者Chen XK(陈兴宽) ; Zheng CW(郑昌武) ; Zhao SL(赵胜利) ; Chai Z(柴卓) ; Yang YQ(杨映权) ; Zhao G(赵刚) ; Cao WG(曹卫国)
刊名Adv. Synth. Catal.
出版日期2010
卷号352期号:10页码:1648-1652
ISSN号1615-4150
其他题名环状1,3-二羰基化合物对β,γ-不饱和α-酮酸酯的高对映选择性迈克加成
通讯作者赵刚 ; 曹卫国
英文摘要A highly enantioselective Michael addition of cyclic 1,3-dicarbonyl compounds to beta,gamma-unsaturated a-keto esters catalyzed by amino acid-derived thiourea-tertiary-amine catalysts is presented. Using 5 mol% of a novel tyrosine-derived thiourea catalyst, a series of chiral coumarin derivatives were obtained in excellent yields (up to 99%) and with up to 96% ee under very mild conditions within a short reaction time.
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/10.1002/adsc.201000045
语种英语
WOS记录号WOS:000280657900015
公开日期2013-02-26
源URL[http://202.127.28.38/handle/331003/20785]  
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
推荐引用方式
GB/T 7714
Chen XK,Zheng CW,Zhao SL,et al. Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to beta,gamma-Unsaturated alpha-Keto Esters[J]. Adv. Synth. Catal.,2010,352(10):1648-1652.
APA 陈兴宽.,郑昌武.,赵胜利.,柴卓.,杨映权.,...&曹卫国.(2010).Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to beta,gamma-Unsaturated alpha-Keto Esters.Adv. Synth. Catal.,352(10),1648-1652.
MLA 陈兴宽,et al."Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to beta,gamma-Unsaturated alpha-Keto Esters".Adv. Synth. Catal. 352.10(2010):1648-1652.

入库方式: OAI收割

来源:上海有机化学研究所

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