Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution
Li GQ(李公强) ; Li Y(李毅) ; Dai LX(戴立信) ; You SL(游书力)
刊名Adv. Synth. Catal.
2008
卷号350期号:9页码:1258-1262
ISSN号1615-4150
其他题名Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution
通讯作者游书力
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.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/adsc.200800071
语种英语
WOS记录号WOS:000256976100013
公开日期2013-02-19
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/15971]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
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.
APA 李公强,李毅,戴立信,&游书力.(2008).Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution.Adv. Synth. Catal.,350(9),1258-1262.
MLA 李公强,et al."Enantioselective synthesis of cis-4-formyl-beta-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution".Adv. Synth. Catal. 350.9(2008):1258-1262.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace