Sammanfattning
One-pot synthesis of R-1-phenylethyl acetate was investigated starting from hydrogenation of acetophenone over a metal-supported catalyst followed by acylation of the formed R-1-phenylethanol over an immobilized lipase. The most promising catalyst for the hydrogenation step was Pd/Al2O3, which in combination with an immobilized lipase yielded maximally 22% R-1-phenylethyl acetate. The support acidity had a crucial effect on the selectivity towards the desired product.
Originalspråk | Engelska |
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Sidor (från-till) | 70-73 |
Antal sidor | 4 |
Tidskrift | Catalysis Today |
Volym | 140 |
Nummer | 1-2 |
DOI | |
Status | Publicerad - 15 feb. 2009 |
MoE-publikationstyp | A1 Tidskriftsartikel-refererad |