Preparation of novel chiral stationary phase based on click chemistry for ligand exchange chromatography

Click chemistry was applied to immobilize L-proline derivative onto azide-modified silica gel to give a novel chiral stationary phase (denoted as click-CSP) for ligand exchange chromatography. The developed protocol combines the benefits of operational simplicity, exceptionally mild conditions and h...

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Bibliographic Details
Published inChinese chemical letters Vol. 20; no. 11; pp. 1345 - 1347
Main Authors Fu, Chun Mei, Shi, Hong Yu, Qian, Guang Sheng, Li, Zhang Wan
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.11.2009
Graduate School of the Chinese Academy of Sciences,Beijing 100049,China
West China School of Pharmacy,Sichuan University,Chengdu 610041,China%Chengdu Institute of Organic Chemistry,Chinese Academy of Sciences,Chengdu 610041,China
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Summary:Click chemistry was applied to immobilize L-proline derivative onto azide-modified silica gel to give a novel chiral stationary phase (denoted as click-CSP) for ligand exchange chromatography. The developed protocol combines the benefits of operational simplicity, exceptionally mild conditions and high surface loadings. The enantioselectivity α of some DL-arnino acids on the click- CSP were found to be in the range from 1.13 to 3.46. The chromatographic resolutions of some DL-amino acids and the stability study firmly illustrate the potential of click chemistry for preparation chiral stationary phase for ligand exchange chromatography.
Bibliography:11-2710/O6
vL-amino acids
Click chemistry; Ligand exchange chromatography; Chiral stationary phase; vL-amino acids
O657.72
Chiral stationary phase
Click chemistry
Ligand exchange chromatography
O629.711
ISSN:1001-8417
1878-5964
DOI:10.1016/j.cclet.2009.05.011