Abstract
AbstractThe title compounds are obtained by a general method involving the sequential stereoselective fluoride‐catalyzed nucleophilic addition of PhSCF2SiMe3 as gem‐difluoromethylene building block to easily available chiral nitrones followed by reductive cleavage of the hydroxy group, N‐alkylation of the obtained pyrrolidines, intramolecular radical cyclization, and hydrogenolysis of the protecting group.
Published Version
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.
