Synthesis of α-hydroxy ketones and vicinal (R,R)-diols by Bacillus clausii DSM 8716T butanediol dehydrogenase
Author:
Affiliation:
1. Institute of Nano- and Biotechnologies
2. Aachen University of Applied Sciences
3. 52428 Jülich
4. Germany
5. IBG-1: Biotechnology
6. Forschungszentrum Jülich
7. 52425 Jülich
Abstract
Reduction of symmetric or asymmetric vicinal diketones with BcBDH leads to the synthesis of either α-hydroxyketones or vicinal diols.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA02066D
Reference50 articles.
1. 2,3-Hexanediols as Sex Attractants and a Female-produced Sex Pheromone for Cerambycid Beetles in the Prionine Genus Tragosoma
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3. New and Convenient Chemoenzymatic Syntheses of (S)-2-Hydroxy-3-octanone, the Major Pheromone Component of Xylotrechus spp., and Its R-Enantiomer
4. Generation of Odorous Acyloins by Yeast Pyruvate Decarboxylases and Their Occurrence in Sherry and Soy Sauce
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