Abstract
A new metastable enol was prepared by the reaction of 2-benzyl acrolein with thiobenzoic acid in aprotic solvents. The enantioselective tautomerization of this enol was studied and enantiomeric excesses up to 71% were found. The absolute configuration of the resulting aldehyde was assigned.
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.
