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学科主题: 金属有机化学
题名: Desymmetrization of Cyclohexadienones via Bronsted Acid-Catalyzed Enantioselective Oxo-Michael Reaction
其他题名: 通过手性布朗斯特酸催化的不对称氧杂Michael反应实现环己二烯酮的去对称化
作者: Gu Q(顾庆) ; Rong ZQ(荣子强) ; Zheng C(郑超) ; You SL(游书力)
通讯作者: 游书力
刊名: J. Am. Chem. Soc.
发表日期: 2010
卷: 132, 期:12, 页:4056-4057
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所
英文摘要: Desymmetrization of cyclohexadienones via enantioselective oxo-Michael reaction catalyzed by chiral phosphoric acid to afford highly enantioenriched 1,4-dioxane and tetrahydrofuran derivatives in excellent yields has been realized. The newly established methodology allows the facile enantioselective synthesis of cleroindicins C, D, and F.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000276009500013
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/22524
Appears in Collections:金属有机化学国家重点实验室_期刊论文

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Recommended Citation:
Gu Q,Rong ZQ,Zheng C,et al. Desymmetrization of Cyclohexadienones via Bronsted Acid-Catalyzed Enantioselective Oxo-Michael Reaction[J]. J. Am. Chem. Soc.,2010,132(12):4056-4057.
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