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12Gaetano Cantarella, Carlo Galli and Patrizia Gentili.
Oxidation of non-phenolic substrates with the laccase/N-hydroxyacetanilide system: Structure of the key intermediate from the mediator and mechanistic insight, New J. Chem., 2004, 28, 366. Jóhannes ReynissonCurrent address: Institute of Cancer Research, Cancer Therapeutics, 15 Cotswold Road, Sutton, Surrey, SM2 5NG, UK. E-mail: Johannes.Reynisson@icr.ac.uk and Steen Steenken.
Hydrogen bonding between histidine and lignin model compounds or redox mediators as calculated with the DFT method. Effects on the ease of oxidation, Org. Biomol. Chem., 2004, 2, 578. Umsetzungen von Acetanilid und Acetylphenylhydroxylamin im Organismus, Naunyn-Schmiedebergs Archiv f??r experimentelle Pathologie und Pharmakologie Investigation of conformational equilibria in a series of substituted N-acetylphenyl hydroxylamines and their methyl ethers by NMR and IR spectroscopy, Journal of Applied Spectroscopy NMR study of retarded internal rotation in N-acetylphenylhydroxylamine and its methyl ether, Journal of Applied Spectroscopy Investigation of hydroxamic acids as laccase-mediators for pulp bleaching, Applied Microbiology and Biotechnology Laccase applications in biofuels production: current status and future prospects, Applied Microbiology and Biotechnology Intensification of Biocatalytical Processes by Synergistic Substrate Conversion. Fungal Peroxidase Catalyzed N-Hydroxy Derivative Oxidation in Presence of 10-Propyl Sulfonic Acid Phenoxazine, Applied Biochemistry and Biotechnology