Sammanfattning
Acylation of (R,S)-1-phenylethanol, which is a product of acetophenone hydrogenation, over a Pd-supported catalyst, was studied in ethyl acetate with an immobilized lipase. It was demonstrated that in the presence of hydrogen and Pd/C in the reaction medium the (R,S)-1-phenylethanol acylation rate is not hindered, whereas the selectivity was strongly altered in the latter case, leading to significant amounts of side products.
Originalspråk | Engelska |
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Sidor (från-till) | 245-252 |
Antal sidor | 8 |
Tidskrift | Research on Chemical Intermediates |
Volym | 36 |
Nummer | 3 |
DOI | |
Status | Publicerad - apr. 2010 |
MoE-publikationstyp | A1 Tidskriftsartikel-refererad |