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Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines
Alternative Title通过钯催化的吲哚啉烯丙基胺化/氧化对映选择性的合成N-烯丙基吲哚
Zhao Q(赵强); Zhuo CX(卓春祥); You SL(游书力)
2014
Source PublicationRSC Adv.
Volume4Issue:21Pages:10875-10878
AbstractA highly efficient synthesis of N-allylindoles was realized via palladium-catalyzed asymmetric allylic amination/oxidation sequential reaction of indolines. The N-alkylated indole derivatives were obtained with up to 91% yield and 97% ee.
Subject Area金属有机化学
DOI10.1039/c4ra00701h
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Indexed BySCI
Language英语
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Cited Times:6[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39040
Collection金属有机化学国家重点实验室
Corresponding AuthorYou SL(游书力)
Affiliation中科院上海有机化学研究所
Recommended Citation
GB/T 7714
Zhao Q,Zhuo CX,You SL. Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines[J]. RSC Adv.,2014,4(21):10875-10878.
APA 赵强,卓春祥,&游书力.(2014).Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines.RSC Adv.,4(21),10875-10878.
MLA 赵强,et al."Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines".RSC Adv. 4.21(2014):10875-10878.
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