Results 161 to 170 of about 5,957 (202)
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Streptavidin chiral stationary phase for the separation of adenosine enantiomers

Journal of Chromatography A, 2004
In this paper, a microbore column packed with streptavidin particles was used, at various temperatures (0-24 degrees C), to separate the adenosine enantiomers by HPLC. Using an aqueous mobile phase, the apparent enantioseparation was high for a small molecule, varying from 11.5 at 0 degrees C to 6.2 at 24 degrees C.
Corinne, Ravelet   +5 more
openaire   +2 more sources

Enantioseparation behavior of chiral stationary phases AD, AS and OD

Chinese Journal of Chromatography, 2016
Over the past decades, HPLC enantioseparation with chiral stationary phases (CSPs) has been widely applied in chiral analysis and preparation of new pharmaceuticals, pesticides, food, etc. Herein, enantioseparation of 20 chiral compounds have been carried out on three polysaccharide-based CSPs (EnantioPak AD, AS and OD) with normal phases by HPLC ...
Liqun, Li   +6 more
openaire   +2 more sources

Chiral Differentiation of Chiral Lactides and Chiral Diketones on Native and Phenylcarbamoylated Cyclodextrin Chiral Stationary Phases

Chirality
ABSTRACTInclusion complexation, hydrogen bonds, π–π interaction, dipole–dipole interaction, and steric hindrance effect all contribute to the enantioseparation ability of cyclodextrin (CD) or CD derivatives. In this work, one native cationic CD chiral stationary phases (SHCDCSP) and four derivatized CD‐CSPs, namely, per(4‐trifluoromethyl ...
Xiaoxuan Li   +3 more
openaire   +2 more sources

Antibody-Mimicking Polymers as Chiral Stationary Phases in HPLC

Analytical Chemistry, 1996
Antibody-mimicking synthetic polymers, selective for various optically active amino acid derivatives and peptides, were prepared by noncovalent molecular imprinting. A novel approach, in which the branched, trifunctional cross-linkers pentaerythritol triacrylate and 2,2-bis(hydroxymethyl)butanol trimethacrylate were copolymerized with methacrylic acid,
openaire   +2 more sources

Chiral stationary phases for the liquid chromatographic separation of pharmaceuticals

Journal of Pharmaceutical and Biomedical Analysis, 1988
Biological systems exhibit remarkable enantioselectivity which is important in biosynthesis, metabolism, storage and transport processes. It is, therefore, not surprising that the chirality of, for example, pharmaceuticals, pesticides and agrochemicals, has become the focus of extensive research in many laboratories throughout the world.
openaire   +2 more sources

Chiral stationary phase design

Journal of Chromatography A, 1993
William H. Pirkle, Patrick G. Murray
openaire   +1 more source

Synthesis and Spectroscopic Evaluation of Chiral Selectors in Crial Stationary Phases

2005
The enhanced demand for enantiomerically pure compounds (EPC) has led to the development of a variety of enantioselective separation methods. Like very useful one emerged liquid chromatography which use chiral stationary phases (CSPs). One of the most used CSPs named brush or Pirkle type CSPs consist of small optically active compounds covalently bound
Kontrec, Darko   +2 more
openaire   +1 more source

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