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- W2053775737 abstract "Novel amylose ester derivatives were synthesized and their chiral recognition abilities as chiral stationary phases for high-performance liquid chromatography were evaluated. Compared with amylose benzoate derivatives, cinnamate derivatives showed a higher chiral recognition ability and some racemates could be efficiently resolved. The recognition abilities of these derivatives varied significantly depending on the types and positions of substituents introduced into the phenyl group. Among the prepared derivatives, the nonsubstituted cinnamate derivative showed a relatively high chiral recognition, and interestingly, its ability was influenced by the preparation conditions of packing materials using silica gel as a support. Novel amylose ester derivatives were synthesized and their chiral recognition abilities as chiral stationary phases for high-performance liquid chromatography were evaluated. Among the prepared derivatives, the nonsubstituted cinnamate derivative showed a relatively high chiral recognition, and interestingly, its ability was influenced by the preparation conditions of packing materials using silica gel as a support." @default.
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- W2053775737 date "2010-01-01" @default.
- W2053775737 modified "2023-09-26" @default.
- W2053775737 title "Enantioseparation using amylose esters as chiral stationary phases for high-performance liquid chromatography" @default.
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- W2053775737 doi "https://doi.org/10.1038/pj.2009.300" @default.
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