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.
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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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