Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andreas Präg"'
Publikováno v:
Chembiochem
Partially reduced aromatic polyketides are bioactive secondary metabolites or intermediates in the biosynthesis of deoxygenated aromatics. For the antibiotic GTRI‐02 (mensalone) in different Streptomyces spp., biosynthesis involving the reduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb8a19fc39985bc8cff2d60413fc53b4
https://doi.org/10.1002/cbic.201900357
https://doi.org/10.1002/cbic.201900357
Autor:
Dennis Wetzl, Michael Müller, Sascha Ferlaino, Hans Iding, Steffen Lüdeke, Andreas Präg, Beat Wirz, Cindy Wechsler, Sebastian Roth, Marija Marolt, Nicolas Sandon
Publikováno v:
Chembiochem : a European journal of chemical biology. 18(17)
NADP(H)-dependent imine reductases (IREDs) are of interest in biocatalytic research due to their ability to generate chiral amines from imine/iminium substrates. In reaction protocols involving IREDs, glucose dehydrogenase (GDH) is generally used to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8bf4ccffed6e27e02fd38214bf89cd2
https://pubmed.ncbi.nlm.nih.gov/28722796
https://pubmed.ncbi.nlm.nih.gov/28722796
Autor:
Lisa Schneider, Andreas Präg, Oliver Einsle, Michael Müller, Stefan Gerhardt, Tobias B. Huber
Publikováno v:
ChemCatChem. 6:2248-2252
The importance and structural diversity of chiral amines is well-demonstrated by the myriad nonenzymatic methods for their chemical production. In nature, the production of amines is performed by transamination rather than by reduction of an imine pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35746b01b5c78b11c3dcf87bdcb5034e
https://doi.org/10.1002/cctc.201402218
https://doi.org/10.1002/cctc.201402218
Autor:
Andriy Luzhetskyy, Steffen Lüdeke, Stefan Günther, Björn Grüning, Michael Müller, Michael Richter, Marta Luzhetska, Marcel Wilde, Andreas Präg, Matthias Häckh
Publikováno v:
Journal of the American Chemical Society. 136:6195-6198
Intermolecular oxidative phenol coupling is the main process in nature for the formation of atroposelective biaryl compounds. Although well defined in plants and fungi, this type of dimerization reaction in bacteria is poorly understood. Therefore, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::599a129bbb75cea08a3eb614ccffd113
https://doi.org/10.1021/ja501630w
https://doi.org/10.1021/ja501630w