Abstract
The reduction of α,β-unsaturated (olefin) carbonyl compounds of the type using a 0.75 wt.% Pd catalyst supported on SiO2−AlPO4 (80∶20 w/w) in a Parr reactor at low hydrogen pressure is reported. Selectivity in the reduction of the C=C bond is 100% in every case, and the nature of the groups A and B affects reaction rate, thus suggesting a 1,4-hydrogen addition mechanism.
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