Reaction of B-2(o-tol)(4) with CO and Isocyanides: Cleavage of the C O Triple Bond and Direct C-H Borylations

The reaction of highly Lewis acidic tetra(o-tolyl) diborane(4) with CO afforded a mixture of boraindane and boroxine by the cleavage of the C O triple bond. C-13 labeling experiments confirmed that the carbon atom in the boraindane stems from CO. Simultaneously, formation of boroxine 3 could be considered as borylene transfer to capture the oxygen atom from CO. The reaction of diborane(4) with Bu-t-NC afforded an azaallene, while the reaction with Xyl-NC furnished cyclic compounds by direct C-H borylations.