Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Judith E. Farnberger"'
Publikováno v:
Microbial Cell Factories, Vol 16, Iss 1, Pp 1-17 (2017)
Abstract Background Transaminases have become a key tool in biocatalysis to introduce the amine functionality into a range of molecules like prochiral α-ketoacids and ketones. However, due to the necessity of shifting the equilibrium towards the pro
Externí odkaz:
https://doaj.org/article/c63de272235d46698fbe306f243d0428
Autor:
Nina Richter, Mattia Lazzarotto, Christopher Grimm, Wolfgang Kroutil, Johanna Schichler, Simona Pompei, Michael Fuchs, Judith E. Farnberger
Publikováno v:
ACS Catalysis
The cleavage of aryl methyl ethers is a common reaction in chemistry requiring rather harsh conditions; consequently, it is prone to undesired reactions and lacks regioselectivity. Nevertheless, O-demethylation of aryl methyl ethers is a tool to valo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45e92f4b599751550533aaa2d81e6f17
http://europepmc.org/articles/PMC7506938
http://europepmc.org/articles/PMC7506938
Autor:
Wolfgang Skibar, Ferdinand Zepeck, Katharina Hiebler, Judith E. Farnberger, Mathias Pickl, Sarah Bierbaumer, Wolfgang Kroutil, Nina Richter
Publikováno v:
Communications Chemistry, Vol 1, Iss 1, Pp 1-8 (2018)
Synthetically established methods for methylation of phenols and demethylation of methyl phenyl ethers rely in general on hazardous reagents or/and harsh reaction conditions and are irreversible. Consequently, alternative regioselective methods for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a083872bf2e82bbb6b8937e9016930ff
http://link.springer.com/article/10.1038/s42004-018-0083-2
http://link.springer.com/article/10.1038/s42004-018-0083-2
Autor:
Fernando López-Gallego, Javier González-Sabín, Nicolás Ríos-Lombardía, Lisa Marx, Judith E. Farnberger, Wolfgang Kroutil, Francisco Morís, Ana I. Benítez-Mateos, Per Berglund
Publikováno v:
Advanced Synthesis & Catalysis
Several chemoenzymatic routes have been explored for the preparation of cinacalcet, a calcimimetic agent. Transaminases (TAs) and ketoreductases (KREDs) turned out to be useful biocatalysts for the preparation of key optically active precursors. Thus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5ddc3b3b5329ac9f4731e978fb2e629
https://doi.org/10.1002/adsc.201701485
https://doi.org/10.1002/adsc.201701485
Autor:
Mathias Pickl, Johann H. Sattler, Georg Steinkellner, Karl Gruber, Ferdinand Zepeck, Robert C. Simon, Christine S. Fuchs, Wolfgang Kroutil, Judith E. Farnberger
Publikováno v:
Advanced Synthesis & Catalysis. 360:768-778
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35bea8305c0942a02194c5b329213049
https://doi.org/10.1002/adsc.201701449
https://doi.org/10.1002/adsc.201701449
Publikováno v:
Microbial Cell Factories, Vol 16, Iss 1, Pp 1-17 (2017)
Microbial Cell Factories
Microbial Cell Factories
Background Transaminases have become a key tool in biocatalysis to introduce the amine functionality into a range of molecules like prochiral α-ketoacids and ketones. However, due to the necessity of shifting the equilibrium towards the product side
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23d027bd8efd0d05603a9106f4a750ba
http://link.springer.com/article/10.1186/s12934-017-0750-5
http://link.springer.com/article/10.1186/s12934-017-0750-5
Autor:
Nina Richter, Ferdinand Zepeck, Christopher Grimm, Simona Pompei, Wolfgang Skibar, Wolfgang Kroutil, Judith E. Farnberger
Publikováno v:
Advanced Synthesis & Catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df75bb15b70b45eaa8361492f1ce7435
https://doi.org/10.1002/adsc.201801590
https://doi.org/10.1002/adsc.201801590
Autor:
Desiree Pressnitz, Nina Richter, Wolfgang Kroutil, Judith E. Farnberger, Horst Lechner, Ferdinand Zepeck
Publikováno v:
Green Chemistry. 17:2952-2958
Chiral amines are important building blocks for fine chemicals and pharmaceuticals. Consequently, various biocatalytic routes in particular using ω-transaminases (ω-TAs) have been developed recently. Although catalysts for the synthesis of both ena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1171a38348c572d3e33e86d21a4df0da
https://doi.org/10.1039/c4gc02363c
https://doi.org/10.1039/c4gc02363c
Autor:
Johann H. Sattler, Ferdinand Zepeck, Nina Richter, Wolfgang Kroutil, Judith E. Farnberger, Christine S. Fuchs, Robert C. Simon
Publikováno v:
Tetrahedron: Asymmetry. 25:284-288
Various enantiocomplementary ω-transaminases (ωTAs) were investigated in kinetic resolution and asymmetric reductive amination reactions to prepare silodosin amine. Whilst the enzymatic kinetic resolution gave moderate to good results with respect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbb5d7f485713fcb0c3bb5eab7c36d3c
https://doi.org/10.1016/j.tetasy.2013.12.012
https://doi.org/10.1016/j.tetasy.2013.12.012
Publikováno v:
ChemInform. 47
During the last decade the use of ω-transaminases has been identified as a very powerful method for the preparation of optically pure amines from the corresponding ketones. Their immense potential for the preparation of chiral amines, together with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feeb3eb6c723ac98e02b7d314b55ed34
https://doi.org/10.1002/chin.201602209
https://doi.org/10.1002/chin.201602209