Welcome to LookChem.com Sign In | Join Free

Science Details

Home > Chemical Encyclopedia > Science List > Details
  • Short communicationFacile determination of the absolute configurations of α-hydroxy acids by chiral derivatization coupled with liquid chromatography–mass spectrometry analysis

  • Add time:09/24/2019    Source:sciencedirect.com

    α-Hydroxy acids are commonly encountered in natural bioactive molecules. For convenient determination of the absolute configurations of α-hydroxy acids, a simple method, named the “O-Marfey method” was developed using a chiral derivatization strategy with (1-fluoro-2,4-dinitrophenyl-5)-l-alanine amide (l-FDAA). The liquid chromatography–mass spectrometry (LC–MS) analysis of the derivatives clearly determined the absolute configurations of various α-hydroxy acids based on their elution times and sequences. This new method is operationally simple with short reaction time and sensitive enough for application at a sub-milligram scale without any purification. This method also enables the simultaneous chirality analysis of α-hydroxy acids and α-amino acids. The absolute configuration of a natural depsipeptide bearing an α-hydroxy acid and α-amino acids was successfully determined by our O-Marfey application.

    We also recommend Trading Suppliers and Manufacturers of L-LEUCIC ACID (cas 13748-90-8). Pls Click Website Link as below: cas 13748-90-8 suppliers

    Prev:Sequential polydepsipeptides containing tripeptide sequences and α-hydroxy acids as biodegradable carriers
    Next:Homologation of α-hydroxy acids to α-unsubstituted β-hydroxy carboxamides via Arndt–Eistert reaction)

  • Back】【Close 】【Print】【Add to favorite
Periodic Table
    Related Products