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Organocatalytic asymmetric chlorinative dearomatization of naphthols
Alternative Title有机催化萘酚的不对称氯化去芳构化反应
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)
2015
Source PublicationChem. Sci.
Volume6Issue:7Pages:4179-4183
AbstractAn 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.
Subtype论文
Subject Area金属有机化学
DOI10.1039/c5sc00494b
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000356176200064
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39609
Collection金属有机化学国家重点实验室
Corresponding AuthorYou SL(游书力)
Affiliation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
Recommended Citation
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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