Enantiomer selective acylation of racemic alcohols by lipases in continuous-flow bioreactors

被引:86
作者
Csajagi, Csaba [1 ]
Szatzker, Gabor [2 ,3 ]
Toke, Eniko Rita [2 ,3 ]
Uerge, Laszlo [1 ]
Darvas, Ferenc [1 ]
Poppe, Laszlo [2 ,3 ]
机构
[1] ThalesNano Nanotechnol Inc, Graphisoft Pk, H-1031 Budapest, Hungary
[2] Budapest Univ Technol & Econ, Hungarian Acad Sci, Dept Organ Chem & Technol, H-1111 Budapest, Hungary
[3] Budapest Univ Technol & Econ, Hungarian Acad Sci, Res Grp Alkaloid Chem, H-1111 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
D O I
10.1016/j.tetasy.2008.01.002
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Continuous-flow mode enantiomer selective acetylations of racemic 1-phenylethanol, 1-cyclohexylethanol, and 1-phenylpropan-2-ol (rac-1a-c, respectively) with vinyl acetate were performed in small stainless steel packed-bed reactors filled with different commercial lipase preparations. In several lipase-filled columns, highly enantiomer selective (E> 100) kinetic resolutions of these alcohols were achieved. In most cases, comparison of the continuous-flow and batch mode (shake flask) biotransformations indicated similar enantiomer selectivities (E) but higher productivities (specific reaction rate: r) in the corresponding continuous-flow reaction. The effect of temperature (0-60 degrees C) and pressure (1-120 bar) on the continuous-flow acetylation of racemic 1-phenylpropan-2-ol was investigated in an immobilized Candida antarctica lipase B (CaLB) filled reactor. Pressure had no significant effect on r and E. Expectedly, a monotonous increase of specific reaction rate (r) was observed within this temperature range. Most surprisingly, the enantiomer selectivity had a maximum (E similar to 25, at 20 degrees C) and a minimum (E similar to 7, at 50 degrees C). The continuous-flow reactions in CaLB-filled columns were successfully applied for preparative scale kinetic resolutions of rac-1a-c. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:237 / +
页数:12
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