Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines

	Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines
其他题名	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
发表期刊	RSC Adv.
卷号	4 期号:21 页码:10875-10878
摘要	A 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.
学科领域	金属有机化学
DOI	10.1039/c4ra00701h
URL	查看原文
收录类别	SCI
语种	英语
引用统计
文献类型	期刊论文
条目标识符	http://ir.sioc.ac.cn/handle/331003/39040
专题	金属有机化学国家重点实验室
通讯作者	You SL(游书力)
作者单位	中科院上海有机化学研究所
推荐引用方式 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.