Articles with "hydroxyacetophenone" as a keyword



Highly efficient bioreduction of 2-hydroxyacetophenone to (S)- and (R)-1-phenyl-1,2-ethanediol by two substrate tolerance carbonyl reductases with cofactor regeneration.

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Published in 2017 at "Journal of biotechnology"

DOI: 10.1016/j.jbiotec.2016.12.016

Abstract: Optically pure 1-phenyl-1,2-ethanediol is a very important chiral building block and intermediate in fine chemical and pharmaceutical industries. Reduction of 2-hydroxyacetophenone provides a straightforward approach to access these important compounds. In this study, two enantiocomplementary… read more here.

Keywords: phenyl ethanediol; carbonyl reductases; cofactor regeneration; ped ped ... See more keywords

Using deep eutectic solvents to improve the biocatalytic reduction of 2-hydroxyacetophenone to (R)-1-phenyl-1,2-ethanediol by Kurthia gibsonii SC0312

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Published in 2020 at "Molecular Catalysis"

DOI: 10.1016/j.mcat.2020.110773

Abstract: Abstract The effects of five deep eutectic solvents (DESs) on the production of (R)-1-phenyl-1,2-ethanediol from 2-hydroxyacetophenone catalyzed by Kurthia gibsonii SC0312 were investigated in this study. Of these, choline chloride/1,4-butanediol (ChCl/Bd) showed excellent biocompatibility and… read more here.

Keywords: phenyl ethanediol; hydroxyacetophenone; gibsonii sc0312;
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The keto–enol equilibrium and thermal conversion kinetics of 2- and 4-hydroxyacetophenone in the gas phase: a DFT study

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Published in 2018 at "Molecular Physics"

DOI: 10.1080/00268976.2017.1374483

Abstract: ABSTRACT Keto–enol tautomeric equilibrium and the mechanism of thermal conversion of 2- and 4-hydroxyacetophenone in gas phase have been studied by means of electronic structure calculations using density functional theory (DFT). A topological analysis of… read more here.

Keywords: mechanism; keto enol; hydroxyacetophenone gas; thermal conversion ... See more keywords