Abstract
A new electrophilic monofluoromethylthiolating reagent
N-fluoromethylthiophthalimide PhthSCH2F 1 was developed. Reagent 1 could
be readily synthesized from easily available starting materials benzyl
mercaptan and CH2FCl in three steps. N-fluoromethylthiophthalimide 1 is
a powerful electrophilic monofluoromethylthiolating reagent that allows
the monofluorome-thylthiolation of a wide range of nucleophiles
including alkynes, aryl/vinyl boronic acids, electron-rich
heteroarenes,-ketoesters and oxindoles, as well as thiols under mild
conditions.