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- W2072639842 abstract "A novel chiral stationary phase (CSP) for high-performance liquid chromatography was prepared by covalently bonding (S)-2,2′-dihydroxy-1,1′-binaphthyl to silica gels. This CSP showed enantioselectivity mainly for secondary and tertiary amines. The experimental results suggested that the free hydroxyl groups of the binaphthol moiety play a very important phase in the retention and the chiral recognition on this CSP. Addition of trifluoroacetic acid or diethylamine to a mobile phase affected the peak shape and the enantioselectivity. Trifluoroacetic acid improved the resolution between enantiomers for many analytes." @default.
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- W2072639842 date "1996-06-01" @default.
- W2072639842 modified "2023-10-18" @default.
- W2072639842 title "Preparation and enantioselectivity of (S)-binaphthol-bonded phase for high-performance liquid chromatography" @default.
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- W2072639842 doi "https://doi.org/10.1016/0021-9673(95)01329-6" @default.
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