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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Published in | Chinese chemical letters Vol. 20; no. 11; pp. 1345 - 1347 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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 |
Subjects | |
Online Access | Get full text |
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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. |
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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 |