中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Aldol Reaction Catalyzed by the Self-assembled Nanostructures of L-Proline Containing Amphiphilic Dipeptide: A Morphological Dependence

文献类型:期刊论文

作者Shao, Mingzhe; Jin, Qingxian; Zhang, Li; Liu, Minghua
刊名CHEMISTRY LETTERS
出版日期2012-10-05
卷号41期号:10页码:1349-1350
ISSN号0366-7022
DOI10.1246/cl.2012.1349
英文摘要An L-proline containing amphiphilic dipeptide was found to self-assemble into nanosphere and nanofiber structures. These nanostructures could catalyze an asymmetric aldol reaction in water. Good reactivity and enantiomeric selectivity was observed for the nanosphere structure. Although the reaction could be catalyzed by the nanofiber structure, its enantioselectivity was remarkably decreased. It was suggested that the appropriate packing of the chiral assemblies can selectively control the access of the reactants and thus lead to a higher enantioselectivity in the chirality matched structures.
语种英语
WOS记录号WOS:000310931600116
出版者CHEMICAL SOC JAPAN
源URL[http://ir.iccas.ac.cn/handle/121111/48699]  
专题中国科学院化学研究所
通讯作者Zhang, Li
作者单位Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, CAS Key Lab Colloid Interface & Chem Thermodynam, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Shao, Mingzhe,Jin, Qingxian,Zhang, Li,et al. Asymmetric Aldol Reaction Catalyzed by the Self-assembled Nanostructures of L-Proline Containing Amphiphilic Dipeptide: A Morphological Dependence[J]. CHEMISTRY LETTERS,2012,41(10):1349-1350.
APA Shao, Mingzhe,Jin, Qingxian,Zhang, Li,&Liu, Minghua.(2012).Asymmetric Aldol Reaction Catalyzed by the Self-assembled Nanostructures of L-Proline Containing Amphiphilic Dipeptide: A Morphological Dependence.CHEMISTRY LETTERS,41(10),1349-1350.
MLA Shao, Mingzhe,et al."Asymmetric Aldol Reaction Catalyzed by the Self-assembled Nanostructures of L-Proline Containing Amphiphilic Dipeptide: A Morphological Dependence".CHEMISTRY LETTERS 41.10(2012):1349-1350.

入库方式: OAI收割

来源:化学研究所

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