Orchestration of concurrent oxidation and reduction cycles for stereoinversion and deracemisation of sec-alcohols

被引:154
|
作者
Voss, Constance V. [1 ]
Gruber, Christian C. [1 ]
Faber, Kurt [1 ]
Knaus, Tanja [2 ]
Macheroux, Peter [2 ]
Kroutil, Wolfgang [1 ]
机构
[1] Graz Univ, Dept Chem Organ & Bioorgan Chem, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Biochem, A-8010 Graz, Austria
基金
奥地利科学基金会;
关键词
D O I
10.1021/ja804816a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Black and white are opposites as are oxidation and reduction. Performing an oxidation, for example, of a sec-alcohol and a reduction of the corresponding ketone in the same vessel without separation of the reagents seems to be an impossible task. Here we show that oxidative cofactor recycling of NADP(+) and reductive regeneration of NADH can be performed simultaneously in the same compartment without significant interference. Regeneration cycles can be run in opposing directions beside each other enabling one-pot transformation of racemic alcohols to one enantiomer via concurrent enantioselective oxidation and asymmetric reduction employing defined alcohol dehydrogenases with opposite stereo- and cofactor-preference. Thus, by careful selection of appropriate enzymes, NADH recycling can be performed in the presence of NADP(+) recycling to achieve overall, for example, deracemisation of sec-alcohols or stereoinversion representing a possible concept for a "green" equivalent to the chemical-intensive Mitsunobu inversion.
引用
收藏
页码:13969 / 13972
页数:4
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