Literature DB >> 15058577

Preparation and chiral recognition of a novel chiral stationary phase for high-performance liquid chromatography, based on mono(6A-N-allylamino-6A-deoxy)-perfunctionalized beta-cyclodextrin and covalently bonded silica gel.

Xiang-Hua Lai1, Siu-Choon Ng.   

Abstract

A novel chiral stationary phase (CSP) was prepared by immobilizing mono(6A-N-allylamino-6A-deoxy)-perphenylcarbamoylated beta-cyclodextrin onto the surface of silica gel via hydrosilylation. The chromatographic properties of this column were tested with a wide range of structurally diverse racemic compounds and drugs under reverse phases. Separation mechanisms involved are also discussed.

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Year:  2004        PMID: 15058577     DOI: 10.1016/j.chroma.2003.11.018

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  3 in total

1.  Chiral recognition of aromatic compounds by beta-cyclodextrin based on bimodal complexation.

Authors:  Wensheng Cai; Yanmin Yu; Xueguang Shao
Journal:  J Mol Model       Date:  2005-05-18       Impact factor: 1.810

Review 2.  Analysis of carbohydrates and glycoconjugates by matrix-assisted laser desorption/ionization mass spectrometry: An update for 2003-2004.

Authors:  David J Harvey
Journal:  Mass Spectrom Rev       Date:  2009 Mar-Apr       Impact factor: 10.946

3.  Linkage of α-cyclodextrin-terminated poly(dimethylsiloxanes) by inclusion of quasi bifunctional ferrocene.

Authors:  Helmut Ritter; Berit Knudsen; Valerij Durnev
Journal:  Beilstein J Org Chem       Date:  2013-07-01       Impact factor: 2.883

  3 in total

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