Synthesis and application of dehydroabietylisothiocyante as a new chiral derivatizing agent for the enantiomeric separation of chiral compounds by capillary electrophoretic
		
		
		
			
Synthesis and application of dehydroabietylisothiocyante as a new chiral derivatizing agent for the enantiomeric separation of chiral compounds by capillary electrophoretic
Engineering Village 2
2006 Elsevier Inc.
Accession number:  06099734020 
 
 Title:  Synthesis and application of dehydroabietylisothiocyante as a new chiral derivatizing agent for the enantiomeric separation of chiral compounds by capillary electrophoretic 
 
 Authors:  Wang, Hengshan; Zhang, Rongcan; Zhao, Shulin; Tang, Lidong; Pan, Yinming  
 
 Author affiliation:  College of Chemistry and Chemical Engineering, Guangxi Normal University, 541004 Guilin, China 
 
 Serial title:  Analytica Chimica Acta 
 
 Abbreviated serial title:  Anal. Chim. Acta 
 
 Volume:  v 560 
 
 Issue:  n 1-2 
 
 Issue date:  Feb 23 2006 
 
 Publication year:  2006 
 
 Pages:  p 64-68 
 
 Language:  English 
 
 ISSN:  0003-2670 
 
 CODEN:  ACACAM 
 
 Document type:  Journal article (JA) 
 
 Publisher:  Elsevier, Amsterdam, 1000 AE, Netherlands 
 
 Abstract:  A new chiral derivatizing reagent, dehydroabietylisothiocyante (DHAIC), was synthesized and used for the enantiomeric separation of chiral compounds in capillary electrophoresis (CE). The synthetic route to obtain DHAIC is described. The separation conditions for the chiral separation of several chiral compounds, such as protein amino acids and chiral drug DOPA were optimized. Best results for the chiral separation of DHAIC derivatized amino acids and DOPA were obtained in a running buffer consisted of 50 mM borate (pH 9.5), 5 mM sodium dodecyl sulphate (SDS) and 20% acetonitrile for amino acids and 60 mM Na2HPO4 (pH 8.0), 17 mM SDS and 25% acetonitrile for DOPA. Under the conditions studied, chiral separation of five amino acids including Ser, Val, Ala, Thr, Cys and a chiral drug DOPA as their diastereomeric DHAIC derivatives has been achieved by micellar electrokinetic chromatography (MEKC). ? 2006 Elsevier B.V. All rights reserved. 
 
 Number of references:  18 
 
 Ei main heading:  Cyanides 
 
 Ei controlled terms:  Synthesis (chemical)  -  Derivatives  -  Electrophoresis  -  Capillarity  -  Amino acids  -  Chromatographic analysis 
 
 Uncontrolled terms:  Enantiomeric separation  -  Capillary electrophoresis  -  Derivatization 
 
 Ei classification codes:  804.2 Inorganic Compounds  -  802.2 Chemical Reactions  -  701.1 Electricity: Basic Concepts & Phenomena  -  801.3 Colloid Chemistry  -  801.4.1 Electrochemistry  -  631.1 Fluid Flow, General  -  804.1 Organic Compounds 
 
 Treatment:  Theoretical (THR) 
 
 DOI:  10.1016/j.aca.2005.12.041 
 
 Database:  Compendex 
 
   Compilation and indexing terms, ? 2006 Elsevier Inc. All rights reserved 
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