Clemens Stueckler

Asymmetric Bioreduction of CC Bonds using Enoate Reductases OPR1, OPR3 and YqjM: Enzyme‐Based Stereocontrol

Mélanie Hall, Clemens Stueckler, Heidemarie Ehammer et al. · Advanced Synthesis & Catalysis · 2008 · 187 citations

Asymmetric Bioreduction of Activated C=C Bonds Using <i>Zymomonas mobilis</i> NCR Enoate Reductase and Old Yellow Enzymes OYE 1–3 from Yeasts

Mélanie Hall, Clemens Stueckler, Bernhard Hauer et al. · European Journal of Organic Chemistry · 2008 · 181 citations

Engineering, Zymomonas Mobilis, Molecular Biology +17

Asymmetric Bioreduction of Activated Alkenes Using Cloned 12‐Oxophytodienoate Reductase Isoenzymes OPR‐1 and OPR‐3 from <i>Lycopersicon esculentum</i> (Tomato): A Striking Change of Stereoselectivity

Mélanie Hall, Clemens Stueckler, Wolfgang Kroutil et al. · Angewandte Chemie International Edition · 2007 · 169 citations · Full text

Plant Physiology, Engineering, Molecular Biology +16

Stereocomplementary Bioreduction of α,β-Unsaturated Dicarboxylic Acids and Dimethyl Esters using Enoate Reductases:  Enzyme- and Substrate-Based Stereocontrol

Clemens Stueckler, Mélanie Hall, Heidemarie Ehammer et al. · Organic Letters · 2007 · 108 citations

The Substrate Spectra of Pentaerythritol Tetranitrate Reductase, Morphinone Reductase, <i>N</i>‐Ethylmaleimide Reductase and Estrogen‐Binding Protein in the Asymmetric Bioreduction of Activated Alkenes

Nicole J. Mueller, Clemens Stueckler, Bernhard Hauer et al. · Advanced Synthesis & Catalysis · 2010 · 84 citations

Biosynthesis, Biotransformation, Biochemistry +15