Demonstration of redox potential of Metschnikowia koreensis for stereoinversion of secondary alcohols/1,2-Diols

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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. This ecofriendly method afforded the product in high yield (88%) and excellent optical purity (>98% ee), minimizing the requirement of multistep reaction and expensive cofactor. © 2014 Vachan Singh Meena et al.

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Meena, V. S., Banoth, L., & Banerjee, U. C. (2014). Demonstration of redox potential of Metschnikowia koreensis for stereoinversion of secondary alcohols/1,2-Diols. BioMed Research International, 2014. https://doi.org/10.1155/2014/410530

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