Article ID Journal Published Year Pages File Type
9614814 Journal of Molecular Catalysis A: Chemical 2005 5 Pages PDF
Abstract
The preferential adsorption of α,β-unsaturated carboxylic acids during their enantioselective hydrogenation over cinchonidine-modified Pd catalysts is directed by the nature of the substituent (alkyl or aryl) situated in β position.
Keywords
Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
Preview
Enantioselective hydrogenation of α,β-unsaturated carboxylic acids over cinchonidine-modified Pd catalysts: effect of substrate structure on the adsorption mode
Authors
, , , ,