Bioreduction of α-Acetoxymethyl Enones: Proposal for an SN2′ Mechanism Catalyzed by Enereductase

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-lactams

(2015) Elisabetta Brenna et al.   ADVANCED SYNTHESIS & CATALYSIS

Enantioselective Synthesis of (R)-2-Arylpropanenitriles Catalysed by Ene-Reductases in Aqueous Media and in Biphasic Ionic Liquid-Water Systems

(2014) Elisabetta Brenna et al.   ChemCatChem

New developments in ‘ene’-reductase catalysed biological hydrogenations

(2014) Helen S Toogood et al.   CURRENT OPINION IN CHEMICAL BIOLOGY

Substrate scope and synthetic applications of the enantioselective reduction of α-alkyl-β-arylenones mediated by Old Yellow Enzymes

(2013) Elisabetta Brenna et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Enantiodivergence in the reduction of α-methyl and α-halomethyl enones by microorganisms

(2013) Bruno R.S. de Paula et al.   TETRAHEDRON-ASYMMETRY

X-ray Crystallography Reveals How Subtle Changes Control the Orientation of Substrate Binding in an Alkene Reductase

(2013) Yuri A. Pompeu et al.   ACS Catalysis

Ene Reductase-Catalysed Synthesis of (R)-Profen Derivatives

(2012) Jörg Pietruszka et al.   ADVANCED SYNTHESIS & CATALYSIS

Cascade Coupling of Ene Reductases with Alcohol Dehydrogenases: Enantioselective Reduction of Prochiral Unsaturated Aldehydes

(2012) Elisabetta Brenna et al.   ChemCatChem

On the stereochemistry of the Baker's Yeast-mediated reduction of regioisomeric unsaturated aldehydes: Examples of enantioselectivity switch promoted by substrate-engineering

(2012) Elisabetta Brenna et al.   JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC

Reductive dehalogenation of β-haloacrylic ester derivatives mediated by ene-reductases

(2012) Gábor Tasnádi et al.   Catalysis Science & Technology

Stereopreferences of Old Yellow Enzymes: Structure Correlations and Sequence Patterns in Enoate Reductases

(2011) Gustav Oberdorfer et al.   ChemCatChem

Asymmetric Synthesis of (R)-3-Hydroxy-2-methylpropanoate (‘Roche Ester’) and Derivatives via Biocatalytic CC-Bond Reduction

(2010) Clemens Stueckler et al.   ADVANCED SYNTHESIS & CATALYSIS

Bioreduction of α-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial™ and Helional™

(2010) Clemens Stueckler et al.   DALTON TRANSACTIONS

Stereochemical Course of Baker's Yeast Mediated Reduction of the Tri- and Tetrasubstituted Double Bonds of Substituted Cinnamaldehydes

(2009) Giovanni Fronza et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors

(2009) Elisabetta Brenna et al.   TETRAHEDRON-ASYMMETRY

Asymmetric Bioreduction of CC Bonds using Enoate Reductases OPR1, OPR3 and YqjM: Enzyme-Based Stereocontrol

(2008) Mélanie Hall et al.   ADVANCED SYNTHESIS & CATALYSIS

Highly Enantioselective Synthesis of Optically Active Ketones by Iridium-Catalyzed Asymmetric Hydrogenation

(2008) Sheng-Mei Lu et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Opposite Stereochemical Courses for Enzyme-Mediated Alkene Reductions of an Enantiomeric Substrate Pair

(2008) Despina J. Bougioukou et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY