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Results: 3
Enzymes in organic chemistry. Part 10: Chemo-enzymatic synthesis of L-phosphaserine and L-phosphaisoserine and enantioseparation of amino-hydroxyethylphosphonic acids by non-aqueous capillary electrophoresis with quinine carbamate as chiral ion pair agent
Authors: Hammerschmidt, F Lindner, W Wuggenig, F Zarbl, E
Citation: F. Hammerschmidt et al., Enzymes in organic chemistry. Part 10: Chemo-enzymatic synthesis of L-phosphaserine and L-phosphaisoserine and enantioseparation of amino-hydroxyethylphosphonic acids by non-aqueous capillary electrophoresis with quinine carbamate as chiral ion pair agent, TETRAHEDR-A, 11(14), 2000, pp. 2955-2964
Direct liquid chromatographic enantioseparation of chiral alpha- and beta-aminophosphonic acids employing quinine-derived chiral anion exchangers: determination of enantiomeric excess and verification of absolute configuration
Authors: Zarbl, E Lammerhofer, M Hammerschmidt, F Wuggenig, F Hanbauer, M Maier, NM Sajovic, L Lindner, W
Citation: E. Zarbl et al., Direct liquid chromatographic enantioseparation of chiral alpha- and beta-aminophosphonic acids employing quinine-derived chiral anion exchangers: determination of enantiomeric excess and verification of absolute configuration, ANALYT CHIM, 404(2), 2000, pp. 169-177
Enzymes in organic chemistry. Part 9: Chemo-enzymatic synthesis of phosphonic acid analogues of L-valine, L-leucine, L-isoleucine, L-methionine and L-alpha-aminobutyric acid of high enantiomeric excess
Authors: Hammerschmidt, F Wuggenig, F
Citation: F. Hammerschmidt et F. Wuggenig, Enzymes in organic chemistry. Part 9: Chemo-enzymatic synthesis of phosphonic acid analogues of L-valine, L-leucine, L-isoleucine, L-methionine and L-alpha-aminobutyric acid of high enantiomeric excess, TETRAHEDR-A, 10(9), 1999, pp. 1709-1721
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