Highlighting the role of the chlorine substituents in the glycopeptide antibiotic balhimycin for chiral recognition in capillary electrophoresis

The vancomycin‐type glycopeptide antibiotic balhimycin (I) and its dehaloanalogue dechlorobalhimycin (III), which is characterized by the total substitution of the two chlorine atoms of I by hydrogen, were employed as chiral selectors for the enantioresolution of 11 racemic dansyl amino acids and si...

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Veröffentlicht in:	Electrophoresis 2006-03, Vol.27 (5-6), p.1154-1162
Hauptverfasser:	Jiang, Zhengjin, Bertazzo, Marcelo, Süssmuth, Roderich D., Yang, Zhuohong, Smith, Norman Williams, Schurig, Volker
Format:	Artikel
Sprache:	eng
Schlagworte:	Anti-Bacterial Agents - chemistry Balhimycin Binding Sites Binding, Competitive Capillary electrophoresis Chlorine - chemistry Electrophoresis, Capillary - methods Enantioseparation Glycopeptide antibiotics Ligands Molecular Structure Stereoisomerism Vancomycin - analogs & derivatives Vancomycin - chemistry
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