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Boron trifluoride is observed to promote a variety of C-H insertion reactions of benzynes bearing pendant alkyl groups. Computations and various mechanistic studies indicate that BF 3 engages the strained π-bond to confer carbene-like character on the adjacent, noncoordinated benzyne carbon. This represents an unprecedented catalytic role for a non-transition metal such as BF 3 .

BF3-Promoted, Carbene-like, C–H Insertion Reactions of Benzynes

BF₃-Promoted, Carbene-like, C–H Insertion Reactions of Benzynes