Abstract
Eight enantiopure (2 S,3 S)-2-aryl-5-oxotetrahydrofuran-3-carboxylic acids have been synthesized. The key step was a highly stereoselective aldol reaction between an N-acyl oxazolidinone and a corresponding aldehyde.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
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.
