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- Bioreduction of α-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial™ and Helional™. Clemens Stueckler, Nicole J. Mueller, Christoph K. Winkler, Silvia M. Glueck, Karl Gruber, Georg Steinkellner, Kurt Faber
, Dalton Trans.
, 2010
, 39
, 8472
- The flavoprotein-catalyzed reduction of aliphatic nitro-compounds represents a biocatalytic equivalent to the Nef-reaction. Katharina Durchschein, Bianca Ferreira-da Silva, Silvia Wallner, Peter Macheroux, Wolfgang Kroutil, Silvia Maria Glueck, Kurt Faber
, Green Chem.
, 2010
, 12
, 616
- Index pages
, Nat. Prod. Rep.
, 1997
, 14
, I1
- Index pages
, Nat. Prod. Rep.
, 1992
, 9
, I1
- Biosynthesis and synthetic biology of psychoactive natural products. Cooper S. Jamieson, Joshua Misa, Yi Tang, John M. Billingsley
, Chem. Soc. Rev.
, 2021
, 50
, 6950
- Enzyme engineering toolbox – a ‘catalyst’ for change. Helen S. Toogood, Nigel S. Scrutton
, Catal. Sci. Technol.
, 2013
, 3
, 2182
- Temperature dependence of dynamic, tunnelling and kinetic isotope effects in formate dehydrogenase. Maite Roca, J. Javier Ruiz-Pernía, Raquel Castillo, Mónica Oliva, Vicent Moliner
, Phys. Chem. Chem. Phys.
, 2018
, 20
, 25722
- Reaction mechanisms: polar reactions. Anna K. Croft, Erika Davies
, Annu. Rep. Prog. Chem., Sect. B: Org. Chem.
, 2011
, 107
, 287
- Enzymatic self-sufficient hydride transfer processes. Erika Tassano, Mélanie Hall
, Chem. Soc. Rev.
, 2019
, 48
, 5596
- Reductive biotransformation of nitroalkenes
via
nitroso-intermediates to oxazetes catalyzed by xenobiotic reductase A (XenA). Katharina Durchschein, Walter M. F. Fabian, Peter Macheroux, Klaus Zangger, Gregor Trimmel, Kurt Faber
, Org. Biomol. Chem.
, 2011
, 9
, 3364