3-[(3-Dehydroabietamidopropyl)dimethylammonio]-1-propane-sulfonate as a new type of chiral surfactant for enantiomer separation in micellar electrokinetic chromatography

Zhao, Shulin; Wang, Hengshan; Pan, Yingming; He, Min; Zhao, Zhicai

doi:10.1016/j.chroma.2007.01.139

Cited by 17 publications

(7 citation statements)

References 18 publications

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“…Recently, novel Rosin- [97,98] and sugar-based chiral surfactants [99,100] have been synthesized and applied to the MEKC enantioseparation of amino acids. In the sugar-based chiral surfactants, it has been revealed that the surfactant structures of the carbohydrate head groups including their anomeric configurations have significant effects on the enantiomeric separation and the migration behavior in MEKC [99].…”

Section: Mekcmentioning

confidence: 99%

Recent progress in capillary electrophoretic analysis of amino acid enantiomers

Kitagawa

Otsuka

2011

Journal of Chromatography B

103

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Section: Mekcmentioning

confidence: 99%

Recent progress in capillary electrophoretic analysis of amino acid enantiomers

Kitagawa

Otsuka

2011

Journal of Chromatography B

103

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“…In both cases, diterpenic acids were used as naturally occurring chiral starting materials. Thus, dehydroabietic acid was employed for the synthesis of 3‐[(3‐dehydroabietamidopropyl)dimethylammonio]‐1‐propanesulfonate 100 and rosin ((−)‐levopimaric acid) was used as starting compound for the preparation of sodium maleopimaric acid 101. With both novel surfactants, several NDA‐AAs such as NDA‐tryptophan (Trp) or NDA‐kynurenine could be baseline resolved using alkaline borate buffer as BGE.…”

Section: Mekc and Meekcmentioning

confidence: 99%

Advances in enantioselective separations using electromigration capillary techniques

2009

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The most recent literature dealing with enantioselective separations and stereoselective analyses of chiral entities including especially pharmaceuticals, phytochemicals, biochemicals, agrochemicals, fine chemicals and specific test compounds by electromigration techniques such as CE, MEKC, MEEKC, CEC and microchip CE is reviewed. The review covers literature from 2007 until mid-2008, i.e. studies that were published after the appearance of the latest review article on that topic in Electrophoresis by Gübitz and Schmid (see Electrophoresis 2007, 28, 114). Particular attention is given to the description of new chiral selector systems, studies on separation mechanisms and applications in the above-specified electromigration techniques.

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“…These compounds were separated using borate buffer and 25 mM surfactant, with resolution for the various compounds in the range of 1.56-5.40 [55].…”

Section: Chiral Surfactantsmentioning

confidence: 99%

Recent advances in amino acid analysis by CE

et al. 2007

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This paper describes a number of articles that have been published on amino acid (AA) analysis using CE during the period from June 2005 to May 2007. This review article follows the format of the previous articles of Smith (Electrophoresis 1999, 20, 3078-3083), Prata et al.. (Electrophoresis 2001, 22, 4129-4138), and Poinsot et al.. (Electrophoresis 2003, 24, 4047-4062 and Electrophoresis 2006, 27, 176-194). Several new developments in AA analysis with CE are reported describing the use of laser-emitting diodes for LIF, MS, and chips. In addition, we describe articles concerning clinical studies and neuroclinical applications.

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3-[(3-Dehydroabietamidopropyl)dimethylammonio]-1-propane-sulfonate as a new type of chiral surfactant for enantiomer separation in micellar electrokinetic chromatography

Cited by 17 publications

References 18 publications

Recent progress in capillary electrophoretic analysis of amino acid enantiomers

Recent progress in capillary electrophoretic analysis of amino acid enantiomers

Advances in enantioselective separations using electromigration capillary techniques

Recent advances in amino acid analysis by CE

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