On the decarboxylation of 2-methyl-1-tetralone-2-carboxylic acid-oxidation of the enol intermediate by triplet oxygen
The formation of 2-methyl-1-tetralone from the metal-free and base-free decarboxylation of 2-methyl-1-tetralone-2-carboxylic acid involves 2-methyl-3,4-dihydro-1-naphthol as an intermediate. The reaction of this enol with atmospheric oxygen leads to 2-hyd
Selective hydrogenation of naphthols to tetralones over supported palladium catalysts in supercritical carbon dioxide solvent
Naphthols were selectively hydrogenated to the corresponding tetralones over supported palladium metal catalysts in supercritical carbon dioxide solvent. Copyright