ENANTIOSELECTIVITY AND REACTIVITY OF IMMOBILIZED LIPASE IN SUPERCRITICAL CARBON-DIOXIDE

被引:22
作者
CERNIA, E [1 ]
PALOCCI, C [1 ]
GASPARRINI, F [1 ]
MISITI, D [1 ]
FAGNANO, N [1 ]
机构
[1] UNIV ROMA LA SAPIENZA,DIPARTIMENTO STUDI CHIM & TECNOL SOSTANZE BIOL ATT,I-00185 ROME,ITALY
来源
JOURNAL OF MOLECULAR CATALYSIS | 1994年 / 89卷 / 1-2期
关键词
CARBON DIOXIDE; ENZYMES; LIPASE; SUPERCRITICAL FLUIDS;
D O I
10.1016/0304-5102(93)E0289-S
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:L11 / L18
页数:8
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