An unprecedented highly stereoselective synthesis of
pyrrolo[1,2-d][1,4]oxazepin-3(2H)-ones has been accomplished
via photoredox/N-heterocyclic carbene (NHC) relay
catalysis. A wide range of substituted dibenzoxazepines and aryl/hetereoaryl
enals were well accommodated under the organic photoredox catalysis-promoted
amine oxidation to generate the imines, followed by a NHC-catalyzed
[3 + 2] annulation reaction to achieve excellent diastereo- and enantioselectivities
of the dibenzoxazepine-fused pyrrolidinones.