Herein, we have developed a complementary
entry to enable hydroheteroarylation
of alkenes involving basically photoredox dearomatizative heterocyclic
carbon radical formation through acid-coupled electron transfer followed
by Giese addition. While protonic solvent and thiophenol additive
enabled two molecular hydroheteroarylations of alkenes, the nonproton
environment with BF3 altered the chemoselectivity over
cascade hydroheteroarylation of alkenes by radical addition of heteroaromatics
with two molecular alkenes. This chemoselectivity can be mechanistically
attributed to the dynamically favored hydrogen atom transfer via the
cyclic transition state.