Organocatalytic asymmetric chlorinative dearomatization of naphthols
Yin Q(殷勤); Wang SG(王守国); Liang XW(梁小伟); Gao DW(高得伟); Zheng J(郑军); You SL(游书力)
刊名Chem. Sci.
2015
卷号6期号:7页码:4179-4183
其他题名有机催化萘酚的不对称氯化去芳构化反应
通讯作者游书力
英文摘要An organocatalytic asymmetric chlorinative dearomatization of naphthols was realized for the first time, providing chiral naphthalenones with a Cl-containing all-substituted stereocenter in excellent yields and enantioselectivity (up to 97% yield and 96% ee). The reaction features mild reaction conditions, good tolerance of diverse functional groups and simple reaction operation.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c5sc00494b
语种英语
WOS记录号WOS:000356176200064
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39609]  
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
推荐引用方式
GB/T 7714
Yin Q,Wang SG,Liang XW,et al. Organocatalytic asymmetric chlorinative dearomatization of naphthols[J]. Chem. Sci.,2015,6(7):4179-4183.
APA 殷勤,王守国,梁小伟,高得伟,郑军,&游书力.(2015).Organocatalytic asymmetric chlorinative dearomatization of naphthols.Chem. Sci.,6(7),4179-4183.
MLA 殷勤,et al."Organocatalytic asymmetric chlorinative dearomatization of naphthols".Chem. Sci. 6.7(2015):4179-4183.
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