Abstract
The asymmetric synthesis of (S)-malic esters was carried out by reduction of β-ketosulfoxides derived from β-ketoesters as well as the transformation of (S)-malic esters into syn and anti-1,2-diols via the reduction of β-keto-γ-alkoxy-sulfoxides. An application to the preparation of 2-deoxy-D-ribose and 2-deoxy-L-xylose derivatives is described.
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.
