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Journal of Biotechnology|July 13, 2020
Process properties of an l-amino acid oxidase from Hebeloma cylindrosporum for the synthesis of phenylpyruvic acid from l-phenylalanineKeiko Oike, Harald GrögerBioorganic & Medicinal Chemistry|August 2, 2014
Enzymatic resolution of racemates with a 'remote' stereogenic center as an efficient tool in drug, flavor and vitamin synthesisMaria Alfaro Blasco, Harald GrögerChemsuschem|June 10, 2024
Overcoming a Conceptual Limitation of Industrial ε-Caprolactone Production via Chemoenzymatic Synthesis in Organic MediumLaura Maria Bernhard, Harald GrögerApplied Microbiology and Biotechnology|January 8, 2010
Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoestersJulia Parkot, Harald Gröger, Werner HummelAngewandte Chemie (International Ed. in English)|February 24, 2015
Cooperative catalysis of noncompatible catalysts through compartmentalization: wacker oxidation and enzymatic reduction in a one-pot process in aqueous mediaHirofumi Sato, Werner Hummel, Harald GrögerApplied Microbiology and Biotechnology|January 25, 2015
Development of a growth-dependent selection system for identification of L-threonine aldolasesDalia Bulut, Harald Gröger, Werner HummelAngewandte Chemie (International Ed. in English)|April 22, 2021
Rationalizing the Unprecedented Stereochemistry of an Enzymatic Nitrile Synthesis through a Combined Computational and Experimental ApproachHilmi Yavuzer, Yasuhisa Asano, Harald GrögerAdvances in Biochemical Engineering/Biotechnology|February 26, 2010
Regeneration of nicotinamide coenzymes: principles and applications for the synthesis of chiral compoundsAndrea Weckbecker, Harald Gröger, Werner HummelACS Catalysis|September 25, 2025
Unlocking the Versatility of Linalool Dehydratase Reactivity: Tunable Stereochemical Control in Olefin Formation via Organic SynthesisJianing Yang, Florian Walkling, Harald GrögerApplied Microbiology and Biotechnology|August 19, 2010
Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydansNina Richter, Harald Gröger, Werner HummelPageof 10