The fusion of transition-metal catalysis with radical chemistry provides a versatile
platform for the asymmetric radical carboazidation of alkenes to enable the rapid
assembly of highly functionalized chiral azide compounds. Here, we present an iron-catalyzed
asymmetric three-component radical carboazidation that processes electron-deficient
alkenes by direct activation of aliphatic C–H bonds. This strategy provides access
to a range of valuable chiral azides from readily available chemical feedstocks bearing
a tetrasubstituted carbon stereocenter, and their synthetic potential is further showcased
through straightforward transformations to provide other valuable enantioenriched
building blocks.
Key words
carboazidation - hydrocarbons - ligands - asymmetric synthesis - radical ligand transfer
- trimethylsilyl azide