strain 发表于 2025-3-27 00:05:45
Enantiomer Separation on Dissolved Cyclodextrin Derivatives by High-Resolution Gas Chromatography: rview on the properties and use of cyclodextrins, a new phase, i.e., heptakis(2,6-O-dimethyl-3-O-heptafluorobutanoyl)-β-cyclodextrin, dissolved in OV-1701 or OV-225 is introduced which shows some complementary behaviour to existing phases in enantiomer separation. For the first time, thermodynamic dneuron 发表于 2025-3-27 02:13:28
Chiral Chromatography on the Process Scale,more practical to use a less complicated synthesis followed by a chromatographic separation of the components of a racemic mixture. This will be true particularly when the unwanted isomers can be recycled back into the synthetic process. However, the relatively low capacity of preparative chromatogr放牧 发表于 2025-3-27 05:47:20
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Optimisation of Chiral Separation of Doxazosin Enantiomers by High-Performance Liquid Chromatograph range 2.6 to 520 ng (on column) with relative standard deviations of 4.0 and 4.9% for the first and second eluting enantiomers, respectively. The limit of detection for the first and second eluting enantiomers, using UV detection at 254 nm, was 1.3 and 1.7 ng, respectively, on column.以烟熏消毒 发表于 2025-3-28 04:20:42
Enantiomer Separation on Dissolved Cyclodextrin Derivatives by High-Resolution Gas Chromatography: ata of enantiomer discrimination involving cyclodextrin derivatives are described. The determination of the temperature dependence of enantiomer separation shows that both the entropie and enthalpie parameters favourably contribute to chiral recognition, and that an isoenantioselective temperature is absent.打包 发表于 2025-3-28 09:29:40
http://reply.papertrans.cn/83/8227/822640/822640_39.png小教堂 发表于 2025-3-28 13:26:38
Chromatographic Chiral Separations on Immobilised Proteins: Does High-Performance Liquid Chromatogrhas demonstrated a direct relationship between . protein binding and chromatographic retention. In addition, the use of enantiomeric solutes has shown that the BSACSP can be used to probe the number and relative affinities of various binding sites on the protein.