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Diastereo- and Enantioselective Catalytic Tandem Michael Addition/Mannich Reaction: Access to Chiral Isoindolinones and Azetidines with Multiple Stereocenters
Department羰基合成与选择氧化国家重点实验室
Guo SM(郭生梅); Xie YJ(谢银君); Hu XQ(胡信全); Xia CG(夏春谷); Huang HM(黄汉民)
2010
Source PublicationAngew. Chem. Int.Ed.
ISSN1521-3773
Volume49Pages:2728-2731
KeywordAsymmetric Catalysis Mannich Reaction Michael Addition Tandem Reactions
Subject Area有机功能材料
Funding Organizationthe Chinese Academy of Sciences and the National Natural Science Foundation of China (20802085,20625308)
Indexed BySCI
Language英语
Funding Project清洁催化与生物转化研究组
Citation statistics
Cited Times:106[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/415
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorHuang HM(黄汉民)
Recommended Citation
GB/T 7714
Guo SM,Xie YJ,Hu XQ,et al. Diastereo- and Enantioselective Catalytic Tandem Michael Addition/Mannich Reaction: Access to Chiral Isoindolinones and Azetidines with Multiple Stereocenters[J]. Angew. Chem. Int.Ed.,2010,49:2728-2731.
APA 郭生梅,谢银君,胡信全,夏春谷,&黄汉民.(2010).Diastereo- and Enantioselective Catalytic Tandem Michael Addition/Mannich Reaction: Access to Chiral Isoindolinones and Azetidines with Multiple Stereocenters.Angew. Chem. Int.Ed.,49,2728-2731.
MLA 郭生梅,et al."Diastereo- and Enantioselective Catalytic Tandem Michael Addition/Mannich Reaction: Access to Chiral Isoindolinones and Azetidines with Multiple Stereocenters".Angew. Chem. Int.Ed. 49(2010):2728-2731.
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