Wolfgang Kroutil
biocatalysis.uni-graz.at
0000-0002-2151-6394
193 papers found
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Cover Feature: Natural Product Diversification by One‐Step Biocatalysis using Human P450 3A4 (ChemCatChem 1/2022)
Natural Product Diversification by One‐Step Biocatalysis using Human P450 3A4
Mechanistic Studies of the TRIP Catalyzed Allylation with Organozinc Reagents
Promiscuous activity of C-acyltransferase from Pseudomonas protegens: synthesis of acetanilides in aqueous buffer
Parallel anti-sense two-step cascade for alcohol amination leading to ω-amino fatty acids and α,ω-diamines
In vivo plug-and-play: a modular multi-enzyme single-cell catalyst for the asymmetric amination of ketoacids and ketones
One-Pot, Two-Module Three-Step Cascade To Transform Phenol Derivatives to Enantiomerically Pure ( R )- or ( S )- p -Hydroxyphenyl Lactic Acids
Enantioselective Reduction of Ethyl 3-Oxo-5-phenylpentanoate with Whole-Cell Biocatalysts
Regio- and Stereoselective Biocatalytic Monoamination of a Triketone Enables Asymmetric Synthesis of Both Enantiomers of the Pyrrolizidine Alkaloid Xenovenine Employing Transaminases
Stereoselective Cascade to C3-Methylated Strictosidine Derivatives Employing Transaminases and Strictosidine Synthases
Biocatalytic One-Pot Synthesis of l -Tyrosine Derivatives from Monosubstituted Benzenes, Pyruvate, and Ammonia
Chemoenzymatic Synthesis towards the Active Agent Travoprost
Inside Cover: Vinylation of Unprotected Phenols Using a Biocatalytic System (Angew. Chem. Int. Ed. 37/2015)
Vinylation of Unprotected Phenols Using a Biocatalytic System
Cobalamin-dependent enzymatic O-, N-, and S-demethylation
Investigation of Structural Determinants for the Substrate Specificity in the Zinc-Dependent Alcohol Dehydrogenase CPCR2 fromCandida parapsilosis
Biocatalytic Imine Reduction and Reductive Amination of Ketones
Cover Picture: Biocatalytic Imine Reduction and Reductive Amination of Ketones (Adv. Synth. Catal. 8/2015)
Biocatalytic Asymmetric Synthesis of Optically Pure Aromatic Propargylic Amines Employing ω-Transaminases
Biocatalysts for the formation of three- to six-membered carbo- and heterocycles
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