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- W2079697561 abstract "Abstract The asymmetric bioreduction of C=C‐bonds bearing an electron‐withdrawing group, such as an aldehyde, ketone, imide, nitro, carboxylic acid, or ester moiety by a novel enoate reductase from Zymomonas mobilis and Old Yellow Enzymes OYE 1–3 from yeasts furnished the corresponding saturated products in up to >99 % ee . Depending on the substrate type, stereocontrol was achieved by variation of the substrate structure, by switching the ( E / Z ) geometry of the alkene or by choice of the appropriate enzyme. This substrate‐ orenzyme‐based stereocontrol allowed access to the opposite enantiomeric products.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)" @default.
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- W2079697561 date "2008-03-01" @default.
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- W2079697561 title "Asymmetric Bioreduction of Activated C=C Bonds Using <i>Zymomonas mobilis</i> NCR Enoate Reductase and Old Yellow Enzymes OYE 1–3 from Yeasts" @default.
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- W2079697561 doi "https://doi.org/10.1002/ejoc.200701208" @default.
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