Divergent reactivity of nucleophilic 1-bora-7a-azaindenide anions

The reactions of 1-bora-7a-azaindenide anions, prepared in moderate to excellent yields by reduction of the appropriate 1-bora-7a-azaindenyl chlorides with KC in THF, with alkyl halides and carbon dioxide were studied. With alkyl halides (CH Cl , CH I and BrCH(D)CH(D) Bu), the anions behave as boron anions, alkylating the boron centre via a classic S 2 mechanism. This was established with DFT methods and via experiments utilizing the neo-hexyl stereoprobe BrCH(D)CH(D) Bu. These reactions were in part driven by a re-aromatization of the six membered pyridyl ring upon formation of the product. Conversely, in the reaction of the 1-bora-7a-azaindenide anions with CO , a novel carboxylation of the C-2 carbon alpha to boron was observed. Computations indicated that while carboxylation of the boron centre was kinetically feasible, the products of B-carboxylation were not thermodynamically favored relative to the observed C-2 carboxylated species, which were formed preferably due to the generation of both C-C and B-O bonds. In these products, the pyridyl ring remains non-aromatic, in part accounting for the observed reversibility of carboxylation.