Here, we report a silver carbene-enabled single-carbon
insertion
reaction of indoles via a one-pot, two-step sequence to deliver a
dearomative quaternary center quinoline scaffold in a modular fashion.
Specifically, we used N-triftosylhydrazones as masked
donor–donor carbene precursors that facilitate the insertion
of carbon atoms bearing various functional groups to the library of
functionalized quinoline. Experimental and DFT evidence support the
transient presence of a cyclopropane species and removal of protecting
groups.