Comparison of several polysaccharide-derived chiral stationary phases for the enantiomer separation ofN-fluorenylmethoxy-carbonyl α-amino acids by hplc-Reference-Cited by-同舟云学术

Comparison of several polysaccharide-derived chiral stationary phases for the enantiomer separation ofN-fluorenylmethoxy-carbonyl α-amino acids by hplc

Published:2007-05 Issue:5 Volume:30 Page:659-664
ISSN:0253-6269
Container-title:Archives of Pharmacal Research
language:en
Short-container-title:Arch Pharm Res

Author:

Jin Jing Yu,Lee Kyung-Ah,Kang Jong Seong,Kang Young Koo,Baek Chae-Sun,Lee Wonjae

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF02977663.pdf

Reference19 articles.

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2. Burgess, K., Solid-Phase Organic Synthesis. John Wiley & Sons Inc, 3rd Ed., New York, (2000).

3. Czerwenka, C., Lämmerhofer, M., and Lindner, W., Structure- enantioselectivity relationships for the study of chiral recognition in peptide enantiomer separation on cinchona alkaloid- based chiral stationary phases by HPLC: Influence of theN- terminal protecting group.J. Sep. Sci., 26, 1499–1508 (2003).

4. Einarsson, S., Folestad, S., Josefsson, B., and Lagerkvist, S., High-resolution reversed-phase liquid chromatography system for the analysis of complex solutions of primary and secondary amino acids.Anal. Chem., 58, 1638–1643 (1986).

5. Ekborg-Ott, K. H., Liu, Y., and Armstrong, D. W., Highly enantioselective HPLC separations using the covalently bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase.Chirality, 10, 434–483 (1998).

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