posted on 2024-08-01, 20:43authored bySuraj Kashyap, Bharat Singh, Manas K. Ghorai
A transition
metal-free, atom-economical, and highly
stereospecific
synthetic approach to Friedel–Crafts-type alkylation of arenes/heteroarenes
has been developed. The protocol involves the catalytic aminium radical-cation
salt (Magic Blue)-initiated SN2-type nucleophilic ring
opening of activated aziridines with arenes/heteroarenes to give the
corresponding 2,2-diarylethylamines up to 99% yield and 85% ee (for
nonracemic aziridines) in a very short reaction time. Moreover, on
reaction with 1,3-dimethylindole and benzofuran, aziridines undergo
domino-ring-opening cyclization (DROC) to give the various biologically
significant heterocyclic scaffolds in moderate to good yields.