The catalytic activity of tris(3,4,5-trifluorophenyl)borane has been explored in the 1,2-hydroboration reactions of unsaturated substrates. Under conventional conditions, the borane was found to be active only in the hydroboration of aldehyde, ketone and imine substrates, with alkenes and alkynes not being reduced effectively. The use of microwave irradiation on the other hand has permitted alkenes and alkynes to be hydroborated in good yields. The experimental and NMR data are provided.
Research
results based upon these data are published at http://doi.org/10.1039/c8cc09459d
Funding
From Organic to Inorganic Chemistry: Exploiting the Isolobal Analogy to Develop Main Group Catalysts
Engineering and Physical Sciences Research Council