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学科主题: 有机化学
题名: Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution
其他题名: Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution
作者: Li GQ(李公强) ; Li Y(李毅) ; Dai LX(戴立信) ; You SL(游书力)
通讯作者: 游书力
刊名: Adv. Synth. Catal.
发表日期: 2008
卷: 350, 期:9, 页:1258-1262
收录类别: SCI
部门归属: 上海有机所
英文摘要: An efficient synthesis of optically pure cis-4-formyl-beta-lactams (up to 99% ee) by a chiral NHC-catalyzed ring expansion reaction has been realized, featuring the ready availability of both the substrate and the catalyst, and the mild reaction conditions. The current method is also suitable for the synthesis of enantioenriched 4-formyl-beta-lactams and succinimides containing quaternary carbon centers.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000256976100013
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/15971
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:
Li GQ,Li Y,Dai LX,et al. Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution[J]. Adv. Synth. Catal.,2008,350(9):1258-1262.
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