Separation and Control of the Elution Order of N-t-Butyloxycarbonyl Amino Acids D/L Isomers by Reversed-phase HPLC Using Cyclodextrins as Chiral Selectors for the Mobile Phase.-Reference-Cited by-同舟云学术

Separation and Control of the Elution Order of N-t-Butyloxycarbonyl Amino Acids D/L Isomers by Reversed-phase HPLC Using Cyclodextrins as Chiral Selectors for the Mobile Phase.

Published:2002 Issue:1 Volume:18 Page:73-76
ISSN:0910-6340
Container-title:Analytical Sciences
language:en
Short-container-title:Anal. Sci.

Author:

WATANABE Shin¹,KAWAHARA Mizue¹,MIURA Kaoru¹,ASO Isao¹

Affiliation:

1. RC Research Laboratory, Tokuyama Corporation

Publisher

Springer Science and Business Media LLC

Subject

Analytical Chemistry

Link

http://www.jstage.jst.go.jp/article/analsci/18/1/18_1_73/_pdf

Reference11 articles.

1. Comparison of enantioselective separation of N-tert.-butyloxycarbonyl amino acids and their non-blocked analogues on teicoplanin-based chiral stationary phase

2. Enantioseparation of selected N-tert.-butyloxycarbonyl amino acids in high-performance liquid chromatography and capillary electrophoresis with a teicoplanin chiral selector

3. Direct separation of carboxylic acid enantiomers by high-performance liquid chromatography with amide and urea derivatives bonded to silica gel as chiral stationary phases

4. Facile Resolution OF N-tert-Butoxy-Carbonyl Amino Acids: The Importance of Enantiomeric Purity in Peptide Synthesis

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