Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions

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	Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions
	Ma AQ(马安琪) ; Ma DW(马大为)
刊名	Org. Lett.
	2010
卷号	12 期号:16 页码:3634-3637
ISSN号	1523-7060
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
通讯作者	马大为
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.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/ol101414b
语种	英语
WOS记录号	WOS:000280799100017
公开日期	2013-02-19
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/15635]
专题	上海有机化学研究所_生命有机化学国家重点实验室
推荐引用方式 GB/T 7714	Ma AQ,Ma DW. Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions[J]. Org. Lett.,2010,12(16):3634-3637.
APA	马安琪,&马大为.(2010).Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions.Org. Lett.,12(16),3634-3637.
MLA	马安琪,et al."Enantioselective Synthesis of Polysubstituted Cyclopentanones by Organocatalytic Double Michael Addition Reactions".Org. Lett. 12.16(2010):3634-3637.