about
A Rapid and High-Throughput Assay for the Estimation of Conversions of Ene-Reductase-Catalysed Reactions.Real-Time Screening of Biocatalysts in Live Bacterial Colonies.Synthetic and Therapeutic Applications of Ammonia-lyases and Aminomutases.Substrate scope and synthetic applications of the enantioselective reduction of α-alkyl-β-arylenones mediated by Old Yellow Enzymes.Investigation of the stereochemical course of ene reductase-catalysed reactions by deuterium labelling.Synthesis of D- and L-phenylalanine derivatives by phenylalanine ammonia lyases: a multienzymatic cascade process.Zymophore identification enables the discovery of novel phenylalanine ammonia lyase enzymes.One-Pot Multi-Enzymatic Synthesis of the Four Stereoisomers of 4-Methylheptan-3-ol.Biosynthesis and Characterization of Copper Nanoparticles Using Shewanella oneidensis: Application for Click Chemistry.Characterisation of a Bacterial Galactokinase with High Activity and Broad Substrate Tolerance for Chemoenzymatic Synthesis of 6-Aminogalactose-1-Phosphate and Analogues.Adenylation Activity of Carboxylic Acid Reductases Enables the Synthesis of Amides.Identification of fungal ene-reductase activity by means of a functional screening.Synthesis of Enantiomerically Pure Ring-Substituted l-Pyridylalanines by Biocatalytic Hydroamination.Rapid and sensitive monitoring of biocatalytic reactions using ion mobility mass spectrometry.One-Pot Biocatalytic Double Oxidation of α-Isophorone for the Synthesis of KetoisophoroneDiscovery and Investigation of Mutase-like Activity in a Phenylalanine Ammonia Lyase from Anabaena variabilis.Engineered Ammonia Lyases for the Production of Challenging Electron-Rich l-PhenylalaninesBiomimetic synthesis of 2-substituted N-heterocycle alkaloids by one-pot hydrolysis, transamination and decarboxylative Mannich reactionBiocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono- and di-amine transaminasesChemoenzymatic Synthesis of Optically Pure l- and d-Biarylalanines through Biocatalytic Asymmetric Amination and Palladium-Catalyzed ArylationThe Bacterial Ammonia Lyase EncP: A Tunable Biocatalyst for the Synthesis of Unnatural Amino AcidsThe characterisation of a galactokinase from Streptomyces coelicolorAsymmetric Bioreduction of β-Acylaminonitroalkenes: Easy Access to Chiral Building Blocks with Two Vicinal Nitrogen-Containing Functional GroupsBiocatalytic synthesis of chiral cyclic γ-oxoesters by sequential C–H hydroxylation, alcohol oxidation and alkene reductionSubstrate Scope Evaluation of the Enantioselective Reduction of β-Alkyl-β-arylnitroalkenes by Old Yellow Enzymes 1-3 for Organic Synthesis ApplicationsCascade Coupling of Ene-Reductases and ω-Transaminases for the Stereoselective Synthesis of Diastereomerically Enriched AminesMulti-enzyme cascade synthesis of the most odorous stereoisomers of the commercial odorant Muguesia®Opposite Enantioselectivity in the Bioreduction of (Z )-β-Aryl-β-cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R )- and (S )-β-Aryl-γ-lactamsSubstrate-engineering approach to the stereoselective chemo-multienzymatic cascade synthesis of Nicotiana tabacum lactoneEnantioselective Synthesis of (R)-2-Arylpropanenitriles Catalysed by Ene-Reductases in Aqueous Media and in Biphasic Ionic Liquid-Water SystemsRationalisation of the stereochemical outcome of ene-reductase-mediated bioreduction of α,β-difunctionalised alkenesOld Yellow Enzyme-mediated reduction of β-cyano-α,β-unsaturated esters for the synthesis of chiral building blocks: stereochemical analysis of the reactionSynthesis of Robalzotan, Ebalzotan, and Rotigotine Precursors via the Stereoselective Multienzymatic Cascade Reduction of α,β-Unsaturated AldehydesCascade Coupling of Ene Reductases with Alcohol Dehydrogenases: Enantioselective Reduction of Prochiral Unsaturated AldehydesEnoate Reductase-Mediated Preparation of Methyl (S)-2-Bromobutanoate, a Useful Key Intermediate for the Synthesis of Chiral Active Pharmaceutical IngredientsProductivity enhancement of CC bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymesStereochemical Outcome of the Biocatalysed Reduction of Activated Tetrasubstituted Olefins by Old Yellow Enzymes 1-3Steric Effects on the Stereochemistry of Old Yellow Enzyme-Mediated Reductions of Unsaturated Diesters: Flipping of the Substrate within the Enzyme Active Site Induced by Structural ModificationsBiocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched α-Halo-β-arylpropionic AcidsEnantioselective CC bond reduction of unsaturated α-chloro esters by old yellow enzymes
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-5861-9269
@en
name
Fabio Parmeggiani
@ast
Fabio Parmeggiani
@en
Fabio Parmeggiani
@es
Fabio Parmeggiani
@nl
type
label
Fabio Parmeggiani
@ast
Fabio Parmeggiani
@en
Fabio Parmeggiani
@es
Fabio Parmeggiani
@nl
prefLabel
Fabio Parmeggiani
@ast
Fabio Parmeggiani
@en
Fabio Parmeggiani
@es
Fabio Parmeggiani
@nl
P106
P21
P31
P496
0000-0001-5861-9269