Encyclopedia

  • Regular paperChloroformates and isothiocyanates derived from 2-arylpropionic acids as chiral reagents: synthetic routes and chromatographic behaviour of the derivatives
  • Add time:09/06/2019         Source:sciencedirect.com

    Chiral derivatization with an enantiomerically pure reagent is an economical and effective way to separate the enantiomers of optically active drugs on achiral HPLC columns. This paper describes the preparation and analytical testing of two novel chiral derivatizing agents (CDAs) deriving from the 2-arylpropionic acid (S)-(+)-naproxen, viz., 1-(6-methoxy-2-naphthyl)ethyl isothiocyanate (NAP-IT) and 2-(6-methoxy-2-naphthyl)-1-propyl chloroformate (NAP-C). Both are suitable reagents for the derivatization of amino compounds (e.g., β-adrenoceptor antagonists, antiarrhythmic agents). The diastereomeric derivatives of these chiral drugs are resolved on reversed-phase HPLC columns and/or silica gel stationary phases. The high UV absorbance and an additional intrinsic fluorescence of both CDAs facilitates the detection of the derivatization products.

    We also recommend Trading Suppliers and Manufacturers of (R)-(-)-1-(1-NAPHTHYL)ETHYL ISOTHIOCYANATE (cas 138617-82-0). Pls Click Website Link as below: cas 138617-82-0 suppliers


    Prev:Anticancer Mechanisms and Researches of Isothiocyanates
    Next: Synthesis and antiproliferative activity of novel α- and β-dialkoxyphosphoryl isothiocyanates)

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View