Hydrodeoxygenation of isocyanates: snapshots of a magnesium-mediated CO bond cleavage

Abstract

-bis(boryl)hemiaminal species have been identified as intermediates during the reductive catalysis, the overall reduction and C-O activation is metal-mediated and proposed to occur through the further intermediacy of well-defined magnesium formamidato, formamidatoborate and magnesium boryloxide derivatives. Examples of all these species have been identified and fully characterised through stoichiometric reactivity studies and the stability of the borate species leads us to suggest that, under catalytic conditions, the onward progress of the deoxygenation reaction is crucially dependent on the further activation provided by the Lewis acidic HBpin substrate. These deductions have been explored and ratified through a DFT study.