Efficient bioreduction of 4-phenyl-2-butanone to drug precursor (S)-4-phenyl-2-butanol by a whole-cell biocatalyst using a novel hybrid design technique-Reference-Cited by-同舟云学术

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Efficient bioreduction of 4-phenyl-2-butanone to drug precursor (S)-4-phenyl-2-butanol by a whole-cell biocatalyst using a novel hybrid design technique

Published:2024-07 Issue: Volume:564 Page:114289
ISSN:2468-8231
Container-title:Molecular Catalysis
language:en
Short-container-title:Molecular Catalysis

Author:

Bayhan Beyzanur,Özdemir Akın,Dertli Enes,Şahin Engin^ORCID

Publisher

Elsevier BV

Reference32 articles.

1. Pharmacologically active compounds in the environment and their chirality;Kasprzyk-Hordern;Chem. Soc. Rev.,2010

2. Extreme halophilic alcohol dehydrogenase mediated highly efficient syntheses of enantiopure aromatic alcohols;Alsafadi;Org. Biomol. Chem.,2017

3. Synthesis of single-enantiomer bioactive molecules: a brief overview;Rouf;Chirality,2014

4. Biocatalysis: synthesis of key intermediates for development of pharmaceuticals;Patel RN;ACS Catal.,2011

5. Pharmacodynamic and pharmacokinetic differences between drug enantiomers in humans: an overview;Drayer;Clin. Pharmacol. Ther.,1986

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