Publication | Open Access
Efficient hydrosilylation of imines using catalysts based on iridium(<scp>iii</scp>) metallacycles
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References
2014
Year
Room TemperatureChemical EngineeringNovel OrganocatalystsEngineeringSlight ExcessOrganic ChemistryEfficient HydrosilylationOrganometallic CatalysisCatalysisMolecular CatalysisChemistryInorganic SynthesisCatalytic SynthesisOrganosilane Reagent
Ir(<bold>iii</bold>) metallacycles were applied as catalysts for the hydrosilylation of ketimines and aldimines by using sodium tetrakis[(3,5-trifluoromethyl)phenyl]borate, NaBArF<sub>24</sub>, as an additive. By using a slight excess of the organosilane reagent, the reactions proceeded rapidly and efficiently, at low catalyst loadings and at room temperature.
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