Some results and some general observations on the reactivity of different substrates in lipase-catalyzed reactions in supercritical carbon dioxide are reported. Chiral 1 -phenylethanol, 2-octanol, 6-methyl-5-hepten-2-ol and trans-3-penten-2-ol have been prepared in high enantiomeric excess (ee > 80%) by enantioselective acetylation of the corresponding racemic alcohols using immobilized crude lipase (Pseudomonas sp. from Amano) in supercritical carbon dioxide.
Enantioselectivity and reactivity of immobilized lipase in supercritical carbon dioxide / Cernia, Enrico; Palocci, Cleofe; Gasparrini, Francesco; Misiti, Domenico; N., Fagnano. - In: JOURNAL OF MOLECULAR CATALYSIS. - ISSN 0304-5102. - STAMPA. - 89(1994), pp. 11-18. [10.1016/0304-5102(93)E0289-S]
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Titolo: | Enantioselectivity and reactivity of immobilized lipase in supercritical carbon dioxide | |
Autori: | ||
Data di pubblicazione: | 1994 | |
Rivista: | ||
Citazione: | Enantioselectivity and reactivity of immobilized lipase in supercritical carbon dioxide / Cernia, Enrico; Palocci, Cleofe; Gasparrini, Francesco; Misiti, Domenico; N., Fagnano. - In: JOURNAL OF MOLECULAR CATALYSIS. - ISSN 0304-5102. - STAMPA. - 89(1994), pp. 11-18. [10.1016/0304-5102(93)E0289-S] | |
Handle: | http://hdl.handle.net/11573/50302 | |
Appartiene alla tipologia: | 01a Articolo in rivista |