Article ID Journal Published Year Pages File Type
10247114 Journal of Molecular Catalysis A: Chemical 2005 6 Pages PDF
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.
Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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