Highly Stereoselective Reductions of α-Alkyl-1,3-diketones and α-Alkyl-β-keto Esters Catalyzed by Isolated NADPH-Dependent Ketoreductases
The biocatalytic reduction of α-alkyl-1,3-diketones and α-alkyl-β-keto esters employing 1 of 20 different isolated NADPH-dependent ketoreductases proved to be a highly efficient method for the preparation of optically pure keto alcohols or hydroxy esters.
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Veröffentlicht in: | Organic letters 2005-10, Vol.7 (22), p.4799-4801 |
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creator | Kalaitzakis, Dimitris Rozzell, J. David Kambourakis, Spiros Smonou, Ioulia |
description | The biocatalytic reduction of α-alkyl-1,3-diketones and α-alkyl-β-keto esters employing 1 of 20 different isolated NADPH-dependent ketoreductases proved to be a highly efficient method for the preparation of optically pure keto alcohols or hydroxy esters. |
doi_str_mv | 10.1021/ol051166d |
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subjects | Catalysis Esters - chemistry Esters - metabolism Ketones - chemistry Ketones - metabolism Molecular Structure NADP - chemistry Oxidation-Reduction Oxidoreductases - chemistry Stereoisomerism |
title | Highly Stereoselective Reductions of α-Alkyl-1,3-diketones and α-Alkyl-β-keto Esters Catalyzed by Isolated NADPH-Dependent Ketoreductases |
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