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- W2364697187 abstract "A chiral stationary phase( CSP) based on amylose 2-benzoate-3-( 3,5-dimethylphenylcarbamate)-6-(( S)-1-phenylethylcarbamate) was prepared,characterized,and evaluated for HPLC enantioseparations under reversed-phase conditions.For the separation of neutral chiral compounds,investigations indicated that the retention and resolution of the racemates were influenced by the nature and the content of the organic additive in the mobile phase.Compared with using acetonitrile as the mobile phase additive,when methanol was used,the CSP exhibited higher chiral recognition and stronger retention was attained.Compared with the resolution data under normal phase conditions,the CSP generally exhibited lower chiral recognition under reversed-phase conditions,while racemate 1was generally better resolved with a higher α value.Also,the resolution of acidic and basic chiral compounds were carried out;however,none of them were separated." @default.
- W2364697187 created "2016-06-24" @default.
- W2364697187 creator A5006532649 @default.
- W2364697187 date "2015-01-01" @default.
- W2364697187 modified "2023-09-24" @default.
- W2364697187 title "Evaluation of Amylose 2-Benzoate-3-( 3,5-dimethylphenylcarbamate)-6-(( S)-1-phenylethylcarbamate) under Reversed-phase Conditions" @default.
- W2364697187 hasPublicationYear "2015" @default.
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