详细信息
A Br?nsted acid-promoted asymmetric intramolecular allylic amination of alcohols ( EI收录)
文献类型:期刊文献
英文题名:A Br?nsted acid-promoted asymmetric intramolecular allylic amination of alcohols
作者:Zhou, Jianqiao[1]; Xie, Hexin[1]
机构:[1] State Key Laboratory of Bioreactor Engineering, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, China
年份:2018
卷号:16
期号:3
起止页码:380
外文期刊名:Organic and Biomolecular Chemistry
收录:EI(收录号:20180404679125)
语种:英文
摘要:Reported herein is a chiral Br?nsted acid-catalyzed asymmetric intramolecular allylic amination reaction, allowing facile access to a range of biologically interesting chiral 2-substituted hydroquinolines in up to 90% yield and with up to 93% ee. Furthermore, a significant effect of an N-protecting group was observed in this asymmetric process. ? 2018 The Royal Society of Chemistry.
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