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Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols

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 an...

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Detalles Bibliográficos
Autores principales: Meena, Vachan Singh, Banoth, Linga, Banerjee, U. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921931/
https://www.ncbi.nlm.nih.gov/pubmed/24592389
http://dx.doi.org/10.1155/2014/410530
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author Meena, Vachan Singh
Banoth, Linga
Banerjee, U. C.
author_facet Meena, Vachan Singh
Banoth, Linga
Banerjee, U. C.
author_sort Meena, Vachan Singh
collection PubMed
description 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.
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spelling pubmed-39219312014-03-03 Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols Meena, Vachan Singh Banoth, Linga Banerjee, U. C. Biomed Res Int Research Article 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. Hindawi Publishing Corporation 2014 2014-01-27 /pmc/articles/PMC3921931/ /pubmed/24592389 http://dx.doi.org/10.1155/2014/410530 Text en Copyright © 2014 Vachan Singh Meena et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Meena, Vachan Singh
Banoth, Linga
Banerjee, U. C.
Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols
title Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols
title_full Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols
title_fullStr Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols
title_full_unstemmed Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols
title_short Demonstration of Redox Potential of Metschnikowia koreensis for Stereoinversion of Secondary Alcohols/1,2-Diols
title_sort demonstration of redox potential of metschnikowia koreensis for stereoinversion of secondary alcohols/1,2-diols
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921931/
https://www.ncbi.nlm.nih.gov/pubmed/24592389
http://dx.doi.org/10.1155/2014/410530
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