中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Michael Addition of Oxindoles to Allenoate Catalyzed by N-Acyl Aminophosphine: Construction of Functionalized Oxindoles with Quaternary Stereogenic Center

文献类型:期刊论文

作者Chen JH(陈锦浩)1; Cai YP(蔡跃鹏)1; Zhao G(赵刚)1
刊名Adv. Synth. Catal.
出版日期2014
卷号356期号:2-3页码:359-363
其他题名氮-乙酰基氨基膦催化氧化吲哚对联烯酸酯不对称加成: 构筑含季碳中心的官能化的氧化吲哚
通讯作者蔡跃鹏 ; 赵刚
英文摘要A novel reaction between ethyl allenoate and oxindoles that enables the asymmetric synthesis of 3,3-bisubstituted oxindoles with our previously established bifunctional N-acyl aminophosphine catalysts is reported. These products bearing a chiral quaternary carbon center at the C-3 position of the oxindoles may have potential significance in the synthesis of related structures. The best performance of these processes provides adducts with 92% yield and 94% ee. imageWILEY-VCH
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.201300695
语种英语
源URL[http://ir.sioc.ac.cn/handle/331003/38972]  
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1.华南师范大学
2.中科院上海有机化学研究所
推荐引用方式
GB/T 7714
Chen JH,Cai YP,Zhao G. Asymmetric Michael Addition of Oxindoles to Allenoate Catalyzed by N-Acyl Aminophosphine: Construction of Functionalized Oxindoles with Quaternary Stereogenic Center[J]. Adv. Synth. Catal.,2014,356(2-3):359-363.
APA 陈锦浩,蔡跃鹏,&赵刚.(2014).Asymmetric Michael Addition of Oxindoles to Allenoate Catalyzed by N-Acyl Aminophosphine: Construction of Functionalized Oxindoles with Quaternary Stereogenic Center.Adv. Synth. Catal.,356(2-3),359-363.
MLA 陈锦浩,et al."Asymmetric Michael Addition of Oxindoles to Allenoate Catalyzed by N-Acyl Aminophosphine: Construction of Functionalized Oxindoles with Quaternary Stereogenic Center".Adv. Synth. Catal. 356.2-3(2014):359-363.

入库方式: OAI收割

来源:上海有机化学研究所

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