Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines

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	Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines
	Dai XY(戴小鸯) ; Wu XY(吴小余) ; Fang HH(房辉辉) ; Nie LL(聂凛凛) ; Chen J(陈结) ; Deng HM(邓红梅) ; Cao WG(曹卫国) ; Zhao G(赵刚)
刊名	Tetrahedron
	2011
卷号	67 期号:17 页码:3034-3040
ISSN号	0040-4020
其他题名	对映选择性有机催化串联反应合成高度官能团化喹嗪烷类生物碱
通讯作者	吴小余 ; 曹卫国 ; 赵刚
英文摘要	An organocatalyzed one-pot Michael addition-Pictet-Spengler sequence of beta-ketoamides and alpha,beta-unsaturated aldehydes was developed, which provided access to highly substituted indolo[2,3-alpha]quinolizidines and benzo[alpha]quinolizidines in moderate to good yields and good to excellent enantioselectivities. For aromatic alpha,beta-unsaturated aldehydes 1a-j products 10a-r containing a stable enol configuration were obtained. (C) 2011 Elsevier Ltd. All rights reserved.
学科主题	天然产物有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1016/j.tet.2011.03.007
语种	英语
WOS记录号	WOS:000290053500003
公开日期	2013-02-26
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/20809]
专题	上海有机化学研究所_中科院天然产物有机化学重点实验室
推荐引用方式 GB/T 7714	Dai XY,Wu XY,Fang HH,et al. Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines[J]. Tetrahedron,2011,67(17):3034-3040.
APA	戴小鸯.,吴小余.,房辉辉.,聂凛凛.,陈结.,...&赵刚.(2011).Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines.Tetrahedron,67(17),3034-3040.
MLA	戴小鸯,et al."Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines".Tetrahedron 67.17(2011):3034-3040.