Asymmetric bioreduction of activated c= c bonds Using Zymomonas mobilis NCR Enoate reductase and Old Yellow Enzymes OYE 1–3 from yeasts
…, C Stueckler, B Hauer, R Stuermer…
Index: Hall, Melanie; Stueckler, Clemens; Hauer, Bernhard; Stuermer, Rainer; Friedrich, Thomas; Breuer, Michael; Kroutil, Wolfgang; Faber, Kurt European Journal of Organic Chemistry, 2008 , # 9 p. 1511 - 1516
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Citation Number: 68
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 ...
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