Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Nina G. Schmidt"'
Publikováno v:
Chemcatchem
Functionalization of aromatic compounds by acylation has considerable significance in synthetic organic chemistry. As an alternative to chemical Friedel‐Crafts acylation, the C‐acyltransferase from Pseudomonas protegens has been found to catalyze
Publikováno v:
Chemical Communications. 54:3387-3390
Amide bond formation has considerable significance in synthetic chemistry. Although the C-acyltransferase from Pseudomonas protegens has been found to catalyze C-C bond formation in nature as well as in in vitro experiments with non-natural substrate
Autor:
Nina G. Schmidt, Wolfgang Kroutil
Publikováno v:
European Journal of Organic Chemistry. 2017:5865-5871
The Friedel–Crafts acylation is a broadly applied reaction that can be conducted using various types of catalyst. However, a biocatalytic alternative has only been reported recently. In this study, the scope of acetyl donors is described, showing t
Autor:
Nina G. Schmidt, Nina Richter, Karl Gruber, Birgit Wiltschi, Wolfgang Kroutil, Tea Pavkov-Keller
Publikováno v:
Angewandte Chemie (International Ed. in English)
The Friedel–Crafts acylation is commonly used for the synthesis of aryl ketones, and a biocatalytic version, which may benefit from the chemo‐ and regioselectivity of enzymes, has not yet been introduced. Described here is a bacterial acyltransfe
Publikováno v:
Advanced Synthesis & Catalysis. 357:1815-1821
Autor:
Birgit Wiltschi, Valerie Ruppert, Anna Żądło-Dobrowolska, Nina G. Schmidt, Wolfgang Kroutil, Christian Höflehner
Publikováno v:
Applied Microbiology and Biotechnology
The formation of C-C bonds by using CoA independent acyltransferases may have significant impact for novel methods for biotechnology. We report the identification of Pseudomonas strains with CoA-independent acyltransferase activity as well as the het
Autor:
Thomas Dr. Haas, Walter M. F. Fabian, Nina G. Schmidt, Kurt Faber, Johannes Gross, Aashrita Rajagopalan, Michael Fuchs, Wolfgang Kroutil, Katharina Tauber, Jan Pfeffer
Publikováno v:
Green Chem.. 16:2117-2121
The oxidation of the renewable diols isosorbide and isomannide was successfully achieved using a TEMPO/laccase system. Furthermore, various TEMPO-derivatives were tested leading to conversions of up to >99% for the oxidation of isosorbide, isomannide
Publikováno v:
ChemInform. 46
Autor:
Christiane Wuensch, Barbara Grischek, Kurt Faber, Johannes Gross, Silvia M. Glueck, Nina G. Schmidt
Publikováno v:
Journal of biotechnology. 168(3)
The enzymatic carboxylation of electron-rich aromatics, which represents a promising 'green' equivalent to the chemical Kolbe-Schmitt reaction, is thermodynamically disfavored and is therefore impeded by incomplete conversions. Optimization of the re
Autor:
Nina G. Schmidt, Tea Pavkov-Keller, Nina Richter, Karl Gruber, Wolfgang Kroutil, Birgit Wiltschi
Publikováno v:
New Biotechnology. 33:S98