American Journal of Analytical Chemistry

Volume 1, Issue 1 (May 2010)

ISSN Print: 2156-8251   ISSN Online: 2156-8278

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Enantioresolution of a Series of Chiral Benzyl Alcohols by HPLC on a Dinitrobenzoylphenylglycine Stationary Phase after Achiral Pre-Column Derivatization*

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DOI: 10.4236/ajac.2010.11001    5,953 Downloads   12,326 Views  Citations

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ABSTRACT

High performance liquid chromatography method for the separation of a series of chiral benzyl alcohols on N-(3,5-dinitrobenzoyl)-D-phenylglycine stationary phase (Macherey Nagel, Chiral-2) after pre-column achiral derivatization was developed. Cheap and easy available aromatic acid chlorides were used as derivatization agents. Good to excellent separations of the enantiomers were achieved in all cases in relatively short analytical runs. It was shown that the enantiorecognition depends on the substituents both in the starting alcohol and in the acid chloride. The method presents an efficient alternative to the direct analyses on polysaccharide and cyclodextrine-derived stationary phases.

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S. Simeonov, A. Simeonov, A. Todorov and V. Kurteva, "Enantioresolution of a Series of Chiral Benzyl Alcohols by HPLC on a Dinitrobenzoylphenylglycine Stationary Phase after Achiral Pre-Column Derivatization*," American Journal of Analytical Chemistry, Vol. 1 No. 1, 2010, pp. 1-13. doi: 10.4236/ajac.2010.11001.

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