Benzoxazines bearing a C4-quaternary stereocenter have been accomplished via the rhodium-catalyzed electrophilic trapping of zwitterionic intermediates by isatins and imines, respectively. The key intermediates of the strategy are proposed to generate from the reaction of donor-acceptor rhodium carbenes with secondary amides. Usage of chiral BINOL-phosphoric acid co-catalyst resulted in enrichment of enantioselectivity in the trapping process with imines.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.9b01207 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!