ENANTIOSEPARATIONS BY CAPILLARY ELECTROPHORESIS USING CHIRAL GLYCOSIDIC SURFACTANTS. II. COMPARISONOF CHIRAL CYCLOHEXYL-ALKYL-β-D-MALTOSIDE SURFACTANTS
ENANTIOSEPARATIONS BY CAPILLARY ELECTROPHORESIS USING CHIRAL GLYCOSIDIC SURFACTANTS. II. COMPARISONOF CHIRAL CYCLOHEXYL-ALKYL-β-D-MALTOSIDE SURFACTANTS
复制标题
使用手性糖苷表面活性剂通过毛细管电泳进行对映体分离 II。
DOI:
10.1081/jlc-100101434
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发表时间:
2000
影响因子:
1.3
通讯作者:
Z. El Rassi
中科院分区:
文献类型:
--
作者:
M. Ju;Z. El Rassi
Three different glycosidic surfactants, namely cyclohexyl-butyl-β-D-maltoside (CYMAL-4), cyclohexyl-pentyl-β-D-maltoside (CYMAL-5), and cyclohexyl-hexyl-β-D-maltoside (CYMAL-6), were compared in the enantioseparation of some dansyl amino acids and methylated tryptophans. The three CYMAL surfactants have the same chiral maltoside head group but differ in the length of the hydrophobic tail. Increasing the length of the hydrophobic tail seems to shift the optimum surfactant concentration for maximum enantioresolution towards lower concentration values. In order to extend the range of optimum surfactant concentration over which maximum enantioresolution can be achieved, mixed CYMAL surfactant systems were introduced and evaluated. They consisted of mixing CYMAL-6 with either cyclohexyl-methyl-β-D-maltoside (CYMAL-1) or cyclohexyl-ethyl-β-D-maltoside (CYMAL-2).