中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly enantioselective hydrogenation of alpha-aryl-beta-substituted acrylic acids catalyzed by Ir-SpinPHOX

文献类型:期刊论文

作者Zhang, Yi1,2; Han, Zhaobin2; Li, Fuying1; Ding, Kuiling2; Zhang, Ao1
刊名CHEMICAL COMMUNICATIONS
出版日期2010
卷号46期号:1页码:156-158
ISSN号1359-7345
DOI10.1039/b919902k
文献子类Article
英文摘要The enantioselective hydrogenation of a series of challenging substrates, alpha-aryl-beta-substituted acrylic acids, was realized with high efficiency and enantioselectivity (up to 96%) under the catalysis of Ir(I) complex of Spiro-based P,N ligand, SpinPHOX.
WOS关键词ALPHA,BETA-UNSATURATED CARBOXYLIC-ACIDS ; ASYMMETRIC HYDROGENATION ; GLUCOKINASE ACTIVATORS ; DIPHOSPHINE LIGANDS ; DIABETES THERAPY ; COMPLEXES ; PSN-GK1 ; AGENTS
资助项目NSFC[20632060] ; NSFC[20821002] ; NSFC[20620140429] ; NSFC[30772625] ; Chinese Academy of Sciences[00000000] ; Major Basic Research Development Program of China[2010CB833300] ; Science and Technology Commission of Shanghai Municipality[00000000] ; Merck Research Laboratories[00000000]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000272679200036
出版者ROYAL SOC CHEMISTRY
源URL[http://119.78.100.183/handle/2S10ELR8/279003]  
专题药物化学研究室
通讯作者Ding, Kuiling
作者单位1.Chinese Acad Sci, Synthet Organ & Med Chem Lab, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
2.Chinese Acad Sci, State Lab Organometall Chem, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China;
推荐引用方式
GB/T 7714
Zhang, Yi,Han, Zhaobin,Li, Fuying,et al. Highly enantioselective hydrogenation of alpha-aryl-beta-substituted acrylic acids catalyzed by Ir-SpinPHOX[J]. CHEMICAL COMMUNICATIONS,2010,46(1):156-158.
APA Zhang, Yi,Han, Zhaobin,Li, Fuying,Ding, Kuiling,&Zhang, Ao.(2010).Highly enantioselective hydrogenation of alpha-aryl-beta-substituted acrylic acids catalyzed by Ir-SpinPHOX.CHEMICAL COMMUNICATIONS,46(1),156-158.
MLA Zhang, Yi,et al."Highly enantioselective hydrogenation of alpha-aryl-beta-substituted acrylic acids catalyzed by Ir-SpinPHOX".CHEMICAL COMMUNICATIONS 46.1(2010):156-158.

入库方式: OAI收割

来源:上海药物研究所

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