High-performance liquid chromatographic separation of enantiomers of 1,1′-binaphthyl-substituted α-aminoisobutyric acid

被引：11
|
作者：
Péter, A
Török, G
Mazaleyrat, JP
Wakselman, M
机构：
[1] Attila Jozsef Univ, Dept Inorgan & Analyt Chem, H-6701 Szeged, Hungary
[2] Univ Versailles, SIRCOB, F-78000 Versailles, France
来源：
JOURNAL OF CHROMATOGRAPHY A | 1997年 / 790卷 / 1-2期
基金：
匈牙利科学研究基金会;
关键词：
enantiomer separation; aminoisobutyric acid; binaphthyl substituted; glycines;
D O I：
10.1016/S0021-9673(97)00750-4
中图分类号：
Q5 [生物化学];
学科分类号：
071010 ; 081704 ;
摘要：
The direct and indirect stereochemical resolution of the enantiomers of free and N-protected (R,S)-2',1':1,2;1 ",2 ":3,4-dinaphthcyclohepta-1,3-diene-6-amino-6-carboxylic acid (Bin) was achieved by high-performance liquid chromatographic methods. The direct separation was carried out on a beta-cyclodextrin-based chiral stationary phase, ChiraDex, and the indirect resolution by applying pre-column derivatization with 2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl isothiocyanate. (C) 1997 Elsevier Science B.V.
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页码：41 / 46
页数：6
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