Stephen P. Thomas, Varinder K. Aggarwal
Abstract
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A breakthrough in the asymmetric hydroboration of notoriously difficult 1,1-disubstituted alkenes using a new family of highly effective hydroboration reagents is described (see scheme). The intermediate boranes can be oxidized to alcohols or used in Suzuki-Miyaura cross-coupling reactions.
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A breakthrough in the asymmetric hydroboration of notoriously difficult 1,1-disubstituted alkenes using a new family of highly effective hydroboration reagents is described (see scheme). The intermediate boranes can be oxidized to alcohols or used in Suzuki-Miyaura cross-coupling reactions.
Key concepts: Hydroboration, Boranes, Chemistry, Reagent, Organic chemistry, Combinatorial chemistry, Coupling (piping), Boron