Abstract
Abstract A novel chiral stationary phase, [(1R,2S)-2-hydroxy-1-methyl-2-phenylethylamino]acetic acid, was prepared from (−)-norephedrine, and its sodium salt was bound to silica gel pretreated with [3-(glycidyloxy)propyl]trimethoxysilane. The chiral stationary phase was found to be effective for the optical resolution of amino acids and their derivatives by ligand-exchange high-performance liquid chromatography using aq copper(II) sulfate solution as an eluent.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
