Chiral separation of amino acids by ligand-exchange capillary electrochromatography using continuous beds

A chiral ligand‐exchange phase for capillary electrochromatography based on continuous bed technology was developed. The chiral stationary phase is prepared by a one‐step in situ copolymerization procedure using methacrylamide, piperazine diacrylamide, vinylsulfonic acid and N‐(2‐hydroxy‐3‐allyloxyp...

Full description

Saved in:
Bibliographic Details
Published inElectrophoresis Vol. 21; no. 15; pp. 3141 - 3144
Main Authors Schmid, Martin G., Grobuschek, Nina, Tuscher, Claudia, Gübitz, Gerald, Végvári, Ákos, Machtejevas, Egidijus, Maruška, Andrius, Hjertén, Stellan
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2000
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A chiral ligand‐exchange phase for capillary electrochromatography based on continuous bed technology was developed. The chiral stationary phase is prepared by a one‐step in situ copolymerization procedure using methacrylamide, piperazine diacrylamide, vinylsulfonic acid and N‐(2‐hydroxy‐3‐allyloxypropyl)‐L‐4‐hydroxyproline. These chiral continuous beds are inexpensive and easy to prepare. They also have several advantages over silica‐based packed capillaries. Since the bed is covalently attached to the capillary wall, no frit is required. The applicability of this new approach to the chiral separation of underivatized amino acids is demonstrated.
Bibliography:ArticleID:ELPS3141
istex:F9B9BD0A03B50FDBD3D4CA78DA78BB3EB8738602
ark:/67375/WNG-NX55R818-5
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0173-0835
1522-2683
DOI:10.1002/1522-2683(20000901)21:15<3141::AID-ELPS3141>3.0.CO;2-T