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Enantiomeric separation of amino acid derivatives by non-aqueous capillary electrophoresis using quinine and related compounds as chiral additives

โœ Scribed by V. Piette; M. Fillet; W. Lindner; J. Crommen

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
47 KB
Volume
14
Category
Article
ISSN
0269-3879

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๐Ÿ“œ SIMILAR VOLUMES

Enantiomeric separation of N-protected a
Enantiomeric separation of N-protected amino acids by non-aqueous capillary electrophoresis using quinine or Tert-butyl carbamoylated quinine as chiral additive
โœ Veronique Piette; Michael Lammerhofer; Wolfgang Lindner; Jacques Crommen ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 137 KB ๐Ÿ‘ 1 views

A capillary electrophoretic (CE) method for the enantioseparation of N-protected chiral amino acids was developed using quinine and tert-butyl carbamoylated quinine as chiral selectors added to nonaqueous electrolyte solutions (NACE). A series of various N-derivatized amino acids were tested as chir

Enantiomeric separation of some amino ac
Enantiomeric separation of some amino acids and derivatives by capillary electrophoresis with 18-crown-6-tetracarboxylic acid as chiral selector
โœ Katleen Verleysen; Pat Sandra ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 124 KB ๐Ÿ‘ 2 views

A number of amino acids and derivatives, bought or synthesized, were ลฝ . analyzed by capillary electrophoresis CE with optical active 18-crown-6-tetra-ลฝ . carboxylic acid 18C6H as chiral selector. Besides the primary interaction, i.e., 4 inclusion of the protonated primary amino function in the crow