Abstrakti
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.
Alkuperäiskieli | Englanti |
---|---|
Sivut | 70-73 |
Sivumäärä | 4 |
Julkaisu | Catalysis Today |
Vuosikerta | 140 |
Numero | 1-2 |
DOI - pysyväislinkit | |
Tila | Julkaistu - 15 helmik. 2009 |
OKM-julkaisutyyppi | A1 Julkaistu artikkeli, soviteltu |