Abstract
The use of gem-bis-metalated-alkenes, i.e.,
vinyl gemdiboron-compound, as light-labile substrates is explored for
the first time. The knowledge gained provided us with an in-depth understanding
of the reactivity of novel radical intermediates of geminal-metalated
ethane. This methodology can serve as the late-stage diversification of
bioactive molecules and simple organic molecules in which it drives the synthesis
of gemdiborylalkanes.