Wolfgang Kroutil
biocatalysis.uni-graz.at
0000-0002-2151-6394
193 papers found
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A Highly Efficient ADH-Coupled NADH-Recycling System for the Asymmetric Bioreduction of Carbon-Carbon Double Bonds Using Enoate Reductases
Old Yellow Enzyme-Catalyzed Dehydrogenation of Saturated Ketones
Biocatalytic Enantioselective Oxidative CC Coupling by Aerobic CH Activation
Bicontinuous Microemulsion as Reaction Medium for ω-Transaminase Catalysed Biotransformations
Enzymatic Racemization of Amines Catalyzed by Enantiocomplementary ω-Transaminases
Creating a Biocatalyst for the Production of an Optically Pure Sterically Hindered Amine
Ostensible Enzyme Promiscuity: Alkene Cleavage by Peroxidases
Novel Developments Employing Redox Enzymes: Old Enzymes in New Clothes
Ketone-Alcohol Hydrogen-Transfer Equilibria: Is the Biooxidation of Halohydrins Blocked?
Testing of microorganisms for ω-transaminase activity
ω-Transaminases for the synthesis of non-racemic α-chiral primary amines
Highly Recyclable Chemo-/Biocatalyzed Cascade Reactions with Ionic Liquids: One-Pot Synthesis of Chiral Biaryl Alcohols
Chemo-promiscuity of alcohol dehydrogenases: reduction of phenylacetaldoxime to the alcohol
Deracemisation of Mandelic Acid to Optically Pure Non-Natural L-Phenylglycine via a Redox-Neutral Biocatalytic Cascade
Immobilization of ω-transaminases by encapsulation in a sol–gel/celite matrix
Cutting Long Syntheses Short: Access to Non-Natural Tyrosine Derivatives Employing an Engineered Tyrosine Phenol Lyase
Deracemisation of Secondary Alcohols via Biocatalytic Stereoinversion
Structural insights into substrate specificity and solvent tolerance in alcohol dehydrogenase ADH-‘A’ from Rhodococcus ruber DSM 44541
Chemoenzymatic asymmetric total synthesis of (S)-Rivastigmine using ω-transaminases
ω-Transaminases as efficient biocatalysts to obtain novel chiral selenium-amine ligands for Pd-catalysis
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