6-O-(Hydroxypropyltrimethylammonia)-β-cyclodextrin with Low Degree of Substitution: Convenient Preparation and its Application as a Chiral Selector in Capillary Electrophoresis

Ming Gang ZHAO Ai You HAO Jian LI Xiu Li LIN

引用本文: Ming Gang ZHAO,  Ai You HAO,  Jian LI,  Xiu Li LIN. 6-O-(Hydroxypropyltrimethylammonia)-β-cyclodextrin with Low Degree of Substitution: Convenient Preparation and its Application as a Chiral Selector in Capillary Electrophoresis[J]. Chinese Chemical Letters, 2006, 17(3): 407-410. shu
Citation:  Ming Gang ZHAO,  Ai You HAO,  Jian LI,  Xiu Li LIN. 6-O-(Hydroxypropyltrimethylammonia)-β-cyclodextrin with Low Degree of Substitution: Convenient Preparation and its Application as a Chiral Selector in Capillary Electrophoresis[J]. Chinese Chemical Letters, 2006, 17(3): 407-410. shu

6-O-(Hydroxypropyltrimethylammonia)-β-cyclodextrin with Low Degree of Substitution: Convenient Preparation and its Application as a Chiral Selector in Capillary Electrophoresis

摘要: A cationic cyclodextrin derivative 6-O-(hydroxypropyltrimethylammonia)-β-cyclodextrin (GTA-β-CD) with low degree of substitution was prepared through a convenient method in solid phase. The product could be used as a valuable chiral selector in the capillary electrophoresis (CE) separation of some acidic drug enantiomers such as naproxen, ofloxacin, ibuprofen and warfarin.

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  • 收稿日期:  2005-09-01
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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