Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins
Ju YD(鞠亚东); Xu LW(徐利文); Li L(李莉); Lai GQ(来国桥); Qiu HY(邱化玉); Jiang JX(蒋剑雄); Lu YX(卢一新)
刊名Tetrahedron Letters
2008
卷号49页码:6773-6777
关键词Primary amine Dual activation Michael addition Organocatalysis
ISSN号0040-4039
通讯作者徐利文
中文摘要Noyori’s Ts-DPEN ligand bearing an amino sulfonamide moiety and with a primary amino group on a chiral scaffold was found to be a simple and efficient bifunctional organocatalyst for the asymmetric Michael addition of 1,3-dicarbonyl compounds to nitroolefins, which gave highly functional Michael adduct with quaternary stereocenters in good enantioselectivities (up to 84%ee) and dr (up to 5.7:1 dr).
学科主题物理化学
收录类别SCI
资助信息Hangzhou Normal University;the National Nature Science Foundation of China (Project No. 20572114)
语种英语
公开日期2012-11-09
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/1979]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
GB/T 7714
Ju YD,Xu LW,Li L,et al. Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins[J]. Tetrahedron Letters,2008,49:6773-6777.
APA Ju YD.,Xu LW.,Li L.,Lai GQ.,Qiu HY.,...&Lu YX.(2008).Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins.Tetrahedron Letters,49,6773-6777.
MLA Ju YD,et al."Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins".Tetrahedron Letters 49(2008):6773-6777.
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