We
describe the first general transition-metal-free synthesis of gem-diboromethyl-substituted bicyclo[1.1.1]pentane (BCP)
and other related C(sp3)-rich carbocyclic
benzene bioisosteres from their corresponding p-tosylhydrazones.
These novel functionalized benzene bioisosteres demonstrated unique
reactivities toward palladium-catalyzed C(sp2)–C(sp3) cross couplings.
The overall transformation can be applied to relatively complex substrates
with potential utility in drug discovery