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学科主题: 有机化学
题名: Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions
其他题名: 通过有机催化的双Michael加成反应对映选择的合成多取代的环戊酮
作者: Ma AQ(马安琪) ; Ma DW(马大为)
通讯作者: 马大为
刊名: Org. Lett.
发表日期: 2010
卷: 12, 期:16, 页:3634-3637
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: The O-TMS-protected diphenylprolinol-catalyzed cascade double Michael addition reactions of alpha,beta-unsaturated aldehydes with a beta-keto ester bearing a highly electron-deficient olefin unit occur smoothly to afford polysubstituted cyclopentanones. This process allows formation of four contiguous stereocenters in the cyclopentanone ring in one-step with excellent enantioselectivity.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000280799100017
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/15635
Appears in Collections:生命有机化学国家重点实验室_期刊论文

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Recommended Citation:
Ma AQ,Ma DW. Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions[J]. Org. Lett.,2010,12(16):3634-3637.
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