中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly Enantioselective Michael Addition of 2-Oxindole-3-carboxylate Esters to Nitroolefins Promoted by Cinchona Alkaloid-Thiourea-Bronsted Acid Cocatalysts

文献类型:期刊论文

作者Chen, Xianjie1,2,3; Zhu, Wei1; Qian, Wangke1; Feng, Enguang1; Zhou, Yu1; Wang, Jinfang1; Jiang, Hualiang1,2,3; Yao, Zhu-Jun2,3; Liu, Hong1
刊名ADVANCED SYNTHESIS & CATALYSIS
出版日期2012-08
卷号354期号:11-12页码:2151-2156
关键词nitroolefins 2-oxindole-3-carboxylate esters spirooxindoles thiourea-Bronsted cocatalysis
ISSN号1615-4150
DOI10.1002/adsc.201200206
文献子类Article
英文摘要A highly efficient organocatalyzed Michael addition of 2-oxindole-3-carboxylate esters to nitroolefins using a Cinchona alkaloid-thiourea and an achiral Bronsted acid as cooperative organocatalysts is reproted that affords significantly improved enantioselectivity and diastereoselectivity. It also provides an efficient approach to the synthesis of spirooxindole derivatives with high enantioselectivity.
WOS关键词PICTET-SPENGLER REACTIONS ; ASYMMETRIC MICHAEL ; CONJUGATE ADDITION ; 3,3'-DISUBSTITUTED OXINDOLES ; QUATERNARY STEREOCENTERS ; 1,3-DICARBONYL COMPOUNDS ; 3-SUBSTITUTED OXINDOLES ; SPIROCYCLIC OXINDOLES ; CONCISE SYNTHESIS ; CONSTRUCTION
资助项目National Basic Research Program of China[2009CB940903] ; National Basic Research Program of China[2012CB518000] ; National Natural Science Foundation of China[20721003] ; National Natural Science Foundation of China[81025017] ; National S&T Major Projects[2012ZX09103-101-072] ; Silver Project[260644]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000307376400016
出版者WILEY-V C H VERLAG GMBH
源URL[http://119.78.100.183/handle/2S10ELR8/277989]  
专题药物化学研究室
中科院受体结构与功能重点实验室
新药研究国家重点实验室
药物发现与设计中心
药理学第一研究室
通讯作者Yao, Zhu-Jun
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
2.Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China;
3.Nanjing Univ, Nanjing Natl Lab Microstruct, Nanjing 210093, Jiangsu, Peoples R China;
推荐引用方式
GB/T 7714
Chen, Xianjie,Zhu, Wei,Qian, Wangke,et al. Highly Enantioselective Michael Addition of 2-Oxindole-3-carboxylate Esters to Nitroolefins Promoted by Cinchona Alkaloid-Thiourea-Bronsted Acid Cocatalysts[J]. ADVANCED SYNTHESIS & CATALYSIS,2012,354(11-12):2151-2156.
APA Chen, Xianjie.,Zhu, Wei.,Qian, Wangke.,Feng, Enguang.,Zhou, Yu.,...&Liu, Hong.(2012).Highly Enantioselective Michael Addition of 2-Oxindole-3-carboxylate Esters to Nitroolefins Promoted by Cinchona Alkaloid-Thiourea-Bronsted Acid Cocatalysts.ADVANCED SYNTHESIS & CATALYSIS,354(11-12),2151-2156.
MLA Chen, Xianjie,et al."Highly Enantioselective Michael Addition of 2-Oxindole-3-carboxylate Esters to Nitroolefins Promoted by Cinchona Alkaloid-Thiourea-Bronsted Acid Cocatalysts".ADVANCED SYNTHESIS & CATALYSIS 354.11-12(2012):2151-2156.

入库方式: OAI收割

来源:上海药物研究所

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