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One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles
Alternative Title一锅法催化不对称合成四氢咔唑
Liu QJ(刘琼杰)1; Yan WG(严文广)1; Wang LJ(王丽佳)1; Zhang XP(张小平)1; Tang Y(唐勇)1
2015
Source PublicationOrg. Lett.
Volume17Issue:16Pages:4014-4017
AbstractA one-pot asymmetric synthesis of 1,2,3,4-tetrahydrocarbizoles has been developed via an enantioselective [3 + 3] annulation of 2-alkynylindoles and donor acceptor cyclopropanes. In the presence of chiral Lewis acids as catalysts, a series of optically active tetrahydrocarbazoles were furnished in high yields (63-87%) With good to excellent levels of enantioselectivity (up to 94% ee).
Subtype论文
Subject Area金属有机化学
DOI10.1021/acs.orglett.5b01909
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000360102900020
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39635
Collection金属有机化学国家重点实验室
Corresponding AuthorZhang XP(张小平); Tang Y(唐勇)
Affiliation1.中科院上海有机化学研究所, 金属有机化学国家重点实验室
2.美国南佛罗里达大学
Recommended Citation
GB/T 7714
Liu QJ,Yan WG,Wang LJ,et al. One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles[J]. Org. Lett.,2015,17(16):4014-4017.
APA 刘琼杰,严文广,王丽佳,张小平,&唐勇.(2015).One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles.Org. Lett.,17(16),4014-4017.
MLA 刘琼杰,et al."One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles".Org. Lett. 17.16(2015):4014-4017.
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