CHIRAL RECOGNITION BY CHROMATOGRAPHY AND COMPUTATIONAL CHEMISTRY

被引:11
作者
HANAI, T [1 ]
HATANO, H [1 ]
NIMURA, N [1 ]
KINOSHITA, T [1 ]
机构
[1] KITASATO UNIV,SCH PHARMACEUT SCI,MINATO KU,TOKYO 108,JAPAN
来源
JOURNAL OF LIQUID CHROMATOGRAPHY | 1993年 / 16卷 / 04期
关键词
D O I
10.1080/10826079308020935
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
After minimization of the energies of individual compounds including a chiral selector using MM2 calculation of CAChe(TM) a pair of molecules was brought together to form a complex, and non-bonded energy was minimized. The energy of R- & S-pairs of alanines and phenylalanines was lower than that of the R- & R- and S- & S-pairs of alanines and phenylalanines. The energy of several pairs of R- & S-N-4-nitrobenzoyl amino acids and a chiral selector, N-butylrylvalinetert-butylamide, also indicated the chiral recognition. The energies of pairs of the selctor and S-amino acids were lower than that of the selector and R-amino acids.
引用
收藏
页码:801 / 808
页数:8
相关论文
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[11]   EFFECT OF APOLAR DILUENTS ON THE BEHAVIOR OF CHIRAL STATIONARY PHASES IN GAS-CHROMATOGRAPHY - BINARY-MIXTURES OF N-LAUROYL-L-VALINE-TERT-BUTYLAMIDE WITH SQUALANE AND N-TETRACOSANE [J].
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