Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10247114 | Journal of Molecular Catalysis A: Chemical | 2005 | 6 Pages |
Abstract
An aqueous palladium catalyst that is stabilized by a water-soluble biquinoline-based ligand was employed for the aerobic oxidation of secondary and primary alcohols. Secondary alcohols afforded the corresponding ketones while aliphatic primary alcohols were fully oxidized to carboxylic acid products. Water is used as the only reaction solvent and air is used as the oxidant, thus these conversions could serve as environmentally benign “green” alternatives to traditional oxidation methods.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Brian P. Buffin, James P. Clarkson, Nadine L. Belitz, Abhijit Kundu,