2014
DOI: 10.1155/2014/410530
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Demonstration of Redox Potential ofMetschnikowia koreensisfor Stereoinversion of Secondary Alcohols/1,2-Diols

Abstract: The present work reports the Metschnikowia koreensis-catalyzed one-pot deracemization of secondary alcohols/1,2-diols and their derivatives with in vivo cofactor regeneration. Reaction is stereoselective and proceeds with sequential oxidation of (R)-secondary alcohols to the corresponding ketones and the reduction of the ketones to (S)-secondary alcohols. Method is applicable to a repertoire of racemic aryl secondary alcohols and 1,2-diols establishing a wide range of substrate specificity of M. koreensis. Thi… Show more

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Cited by 4 publications
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“…[94] This transformation was stereoselective and consisted of the sequential oxidation of the (R)-alcohol and subsequent reduction of the ketone formed to the (S)-enantiomer in high conversion (>88%) and excellent optical purity (>98%) in aqueous medium at 30 ºC.…”
Section: Stereoinversions Over Alcohol Derivatives Using Oxidoreductasesmentioning
confidence: 99%
“…[94] This transformation was stereoselective and consisted of the sequential oxidation of the (R)-alcohol and subsequent reduction of the ketone formed to the (S)-enantiomer in high conversion (>88%) and excellent optical purity (>98%) in aqueous medium at 30 ºC.…”
Section: Stereoinversions Over Alcohol Derivatives Using Oxidoreductasesmentioning
confidence: 99%