Enantiorecognition ability of peptoids with α-chiral, aromatic side chains

被引：14
|
作者：
Wu, Haibo [1 ]
Liang, Tu [1 ]
Yin, Chenghua [1 ]
Jin, Yu [1 ]
Ke, Yanxiong [1 ]
Liang, Xinmiao [1 ,2 ]
机构：
[1] E China Univ Sci & Technol, Sch Pharm, Minist Educ, Engn Res Ctr Pharmaceut Proc Chem, Shanghai 200237, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
来源：
ANALYST | 2011年 / 136卷 / 21期
关键词：
STATIONARY PHASES; RECOGNITION; CHROMATOGRAPHY; DERIVATIVES; RESOLUTION; OLIGOMERS; LENGTH; SEPARATION; SELECTORS; SILICA;
D O I：
10.1039/c1an15485k
中图分类号：
O65 [分析化学];
学科分类号：
070302 ; 081704 ;
摘要：
The enantiorecognition ability of oligomeric N-substituted glycines or "peptoids" with alpha-chiral, aromatic side chains was investigated by HPLC and H-1 NMR studies.
引用
收藏
页码：4409 / 4411
页数：3
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