Enantioselective Construction of Spiroindolenines by Ir-Catalyzed Allylic Alkylation Reactions
Wu QF(武庆锋) ; He H(贺虎) ; Liu WB(刘文博) ; You SL(游书力)
刊名J. Am. Chem. Soc.
2010
卷号132期号:33页码:11418-11419
ISSN号0002-7863
其他题名金属铱催化Spiroindolenine骨架的不对称构建
通讯作者游书力
英文摘要With 2-methyl-1,2,3,4-tetrahydroquinoline-derived phosphoramidite ligand (R,R-a)-L-6, Ir-catalyzed intramolecular C-3 allylic alkylation of indoles has been realized to afford highly enantioenriched spiroindolenine derivatives in 92-98% yields with up to >99/1 dr and 97% ee.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ja105111n
语种英语
WOS记录号WOS:000281066400012
公开日期2013-03-04
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/22512]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Wu QF,He H,Liu WB,et al. Enantioselective Construction of Spiroindolenines by Ir-Catalyzed Allylic Alkylation Reactions[J]. J. Am. Chem. Soc.,2010,132(33):11418-11419.
APA 武庆锋,贺虎,刘文博,&游书力.(2010).Enantioselective Construction of Spiroindolenines by Ir-Catalyzed Allylic Alkylation Reactions.J. Am. Chem. Soc.,132(33),11418-11419.
MLA 武庆锋,et al."Enantioselective Construction of Spiroindolenines by Ir-Catalyzed Allylic Alkylation Reactions".J. Am. Chem. Soc. 132.33(2010):11418-11419.
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