Abstract
Abstract A method is described for the diastereomeric resolution of carotenoids with an 2-hydroxy-β-end group (β,β-caroten-2-ol and β,β-carotene-2,2′-diol) and an 2-hydroxy-4-oxo-β-end group (2-hydroxyechinenone). The separation of each carotenoid into individual optical isomers was achieved by using a chiral resolution column, Sumipax OA-2000, after conversion into the corresponding benzoates.
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.
