2,2,2-TRIFLUOROETHYL CHLOROFORMATE AS A RAPID DERIVATIZING REAGENT OF AMINO-ACIDS FOR FAST ENANTIOMER SEPARATION BY GAS-CHROMATOGRAPHY

被引:11
作者
ABE, I
FUJIMOTO, N
NAKAHARA, T
机构
关键词
D O I
10.1246/cl.1995.113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amino acids were derivatized rapidly into N(O)-2,2,2-trifluoroethoxycarbonyl 2',2',2'-trifluoroethyl esters for enantiomer separation by chiral phase capillary gas chromatography. All the derivatives showed considerable reduction in retention times compared with N(O)-ethoxycarbonyl ethyl ester derivatives with almost complete separation of their enantiomers.
引用
收藏
页码:113 / 114
页数:2
相关论文
共 4 条
[1]   ENANTIOMER SEPARATION OF AMINO-ACIDS AFTER DERIVATIZATION WITH ALKYL CHLOROFORMATES BY CHIRAL PHASE CAPILLARY GAS-CHROMATOGRAPHY [J].
ABE, I ;
NISHIYAMA, T ;
NAKAHARA, T .
ANALYTICAL SCIENCES, 1994, 10 (03) :501-504
[2]  
ABE I, 1994, J HIGH RES CHROMATOG, V17, P9
[3]   RAPID DERIVATIZATION AND GAS-CHROMATOGRAPHIC DETERMINATION OF AMINO-ACIDS [J].
HUSEK, P .
JOURNAL OF CHROMATOGRAPHY, 1991, 552 (1-2) :289-299
[4]  
Konig W. A., 1987, PRACTICE ENANTIOMER