Solvent‐Promoted Oxidation of Aromatic Alcohols/Aldehydes to Carboxylic Acids by a Laccase‐TEMPO System: Efficient Access to 2,5‐Furandicarboxylic Acid and 5‐Methyl‐2‐Pyrazinecarboxylic Acid
A practical and eco-friendly protocol for the oxidation of alcohols into carboxylic acids and ketones under metal-, base- and additive-free conditions is reported.
A simple, efficient, sustainable and economical method for the oxidation of alcohols and amines has been developed using chloride, a sea abundant anionic catalyst for the synthesis of a range of carboxylic acids, ketones and imines.