Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Philipp N. Scheller"'
Autor:
Lars Lauterbach, Niels Borlinghaus, Bettina M. Nestl, Bernhard Hauer, Anne-Sophie Coquel, Claus Lattemann, Leonie Weinmann, Philipp N. Scheller, Florian Krimpzer, Ammar Al-Shameri
Publikováno v:
ChemCatChem. 11:5738-5742
Autor:
Ammar Al-Shameri, Niels Borlinghaus, Leonie Weinmann, Philipp N. Scheller, Bettina M. Nestl, Lars Lauterbach
Publikováno v:
Green Chemistry. 21:1396-1400
We designed a novel H2-driven cascade for the biosynthesis ofN-heterocycles.
Publikováno v:
Protein Expression and Purification. 133:199-204
The reductive amination is one of the most important reactions in the synthesis of chiral amines. Imine reductases (IREDs) are novel enzymes that catalyze the asymmetric reduction of imines and reductive aminations using NADPH as hydride donor. In th
Publikováno v:
Proteins: Structure, Function, and Bioinformatics. 84:600-610
Chiral amines are valuable building blocks for the production of a variety of pharmaceuticals, agrochemicals and other specialty chemicals. Only recently, imine reductases (IREDs) were discovered which catalyze the stereoselective reduction of imines
Publikováno v:
Proteins. 84(5)
Chiral amines are valuable building blocks for the production of a variety of pharmaceuticals, agrochemicals and other specialty chemicals. Only recently, imine reductases (IREDs) were discovered which catalyze the stereoselective reduction of imines
Imine reductases (IREDs) have emerged as promising biocatalysts for the synthesis of chiral amines. In this study, the asymmetric imine reductase-catalyzed intermolecular reductive amination with NADPH as the hydrogen source was investigated. A highl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b4c788e3fb8ea8cdccf738607368637
https://pub.uni-bielefeld.de/record/2949723
https://pub.uni-bielefeld.de/record/2949723
Autor:
Philipp N. Scheller, Bernhard Hauer, Nicholas J. Turner, Jürgen Pleiss, Friedemann Leipold, Silvia Fademrecht, Sebastian Hofelzer, Bettina M. Nestl
Publikováno v:
Scheller, P N, Fademrecht, S, Hofelzer, S, Pleiss, J, Leipold, F, Turner, N, Nestl, B & Hauer, B 2014, ' Enzyme Toolbox: Novel Enantiocomplementary Imine Reductases ', CHEMBIOCHEM, vol. 15, no. 15, pp. 2201-2204 . https://doi.org/10.1002/cbic.201402213
Reducing reactions are among the most useful transformations for the generation of chiral compounds in the fine-chemical industry. Because of their exquisite selectivities, enzymatic approaches have emerged as the method of choice for the reduction o
Publikováno v:
Proteins: Structure, Function, and Bioinformatics. 84:C4-C4