Highly Stereoselective 7-Endo-Trig/Ring Contraction Cascade To Construct Pyrrolo[1,2-a]quinoline Derivatives
Li XY(李新宇) ; Li C(李程) ; Zhang WJ(张文婧) ; Lu X(鲁翔) ; Han SQ(韩世清) ; Hong R(洪然)
刊名Org. Lett.
2010
卷号12期号:8页码:1696-1699
ISSN号1523-7060
其他题名高立体选择性的7-Endo-Trig/缩环串联反应合成吡咯[1,2-a]喹啉衍生物
通讯作者洪然
英文摘要With the cooperation of Cram's phenonium ion, a novel cascade reaction was illustrated to construct pyrrolo[1,2-a]quinolines as a sole diastereoisomer in good to excellent yields. Preliminary mechanistic studies revealed that the gamma-lactam ring and electron-rich arene are important driving forces for ring contraction.
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/10.1021/ol100220c
语种英语
WOS记录号WOS:000276562600013
公开日期2013-08-29
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/28583]  
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
Li XY,Li C,Zhang WJ,et al. Highly Stereoselective 7-Endo-Trig/Ring Contraction Cascade To Construct Pyrrolo[1,2-a]quinoline Derivatives[J]. Org. Lett.,2010,12(8):1696-1699.
APA 李新宇,李程,张文婧,鲁翔,韩世清,&洪然.(2010).Highly Stereoselective 7-Endo-Trig/Ring Contraction Cascade To Construct Pyrrolo[1,2-a]quinoline Derivatives.Org. Lett.,12(8),1696-1699.
MLA 李新宇,et al."Highly Stereoselective 7-Endo-Trig/Ring Contraction Cascade To Construct Pyrrolo[1,2-a]quinoline Derivatives".Org. Lett. 12.8(2010):1696-1699.
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