Pascal Weingart, Patrick Hütchen, Angelo Damone, Maximilian Kohns, Hans Hasse, Werner R. Thiel

• The Griffith-Ley oxidation of alcohols to aldehydes and ketones is performed with either RuCl3 ⋅ (H2O)x or a highly stable, well-defined ruthenium catalyst and with cheap trimethylamine N-oxide (TMAO) as the oxygen source. The use of n-heptane as the solvent, which forms a second phase with TMAO and a part of the alcohol, allows the reactions to be performed with a minimum amount of catalyst. This results in high local concentrations and thus to very rapid conversions. Detailed quantum chemical calculations suggest, that the Griffith-Ley oxidation not necessarily requires high oxidation states of ruthenium but can also proceed with RuII/RuIV species.