Asymmetric Dearomatization of beta-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction

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	Asymmetric Dearomatization of beta-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction
	Wang SG(王守国)1; Liu XJ(刘喜佳)1; Zhao QC(赵群超)1; Zheng C(郑超)1; Wang SB(王少博)1; You SL(游书力)1
刊名	Angew. Chem.-Int. Edit.
	2015
卷号	54 期号:49 页码:14929-14932
其他题名	双功能硫脲催化的Michael反应实现β-萘酚的不对称去芳构化
通讯作者	游书力
英文摘要	An intermolecular asymmetric dearomatization reaction of beta-naphthols with nitroethylene through a chiralthiourea-catalyzed Michael reaction is described. Enantioen-riched functionalized beta-naphthalenones with an all-carbon quaternary stereogenic center could thus be easily constructed from simple naphthol derivatives in good yields and excellent enantioselectivity (up to 79% yield, 98% ee).
学科主题	金属有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1002/anie.201507998
语种	英语
WOS记录号	WOS:000367723400062
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/39683]
专题	上海有机化学研究所_金属有机化学国家重点实验室
作者单位	1.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.天津化学化工协同创新中心
推荐引用方式 GB/T 7714	Wang SG,Liu XJ,Zhao QC,et al. Asymmetric Dearomatization of beta-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction[J]. Angew. Chem.-Int. Edit.,2015,54(49):14929-14932.
APA	王守国,刘喜佳,赵群超,郑超,王少博,&游书力.(2015).Asymmetric Dearomatization of beta-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction.Angew. Chem.-Int. Edit.,54(49),14929-14932.
MLA	王守国,et al."Asymmetric Dearomatization of beta-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction".Angew. Chem.-Int. Edit. 54.49(2015):14929-14932.