Selenocatalytic alpha-halogenation.
Through a 2e- oxidation-reduction cycle, phenylselenides catalytically activate N-chlorosuccinimide toward electrophilic reactions with ketones, resulting in alpha-haloketones.
Journal Article↗
Biomedical subjects
Publications and source records attributed to Jon Tunge.
Through a 2e- oxidation-reduction cycle, phenylselenides catalytically activate N-chlorosuccinimide toward electrophilic reactions with ketones, resulting in alpha-haloketones.