Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Birgit Seisser"'
Autor:
Juergen Eck, Anita Emmerstorfer, Lucas Hammerer, Birgit Seisser, Wolfgang Kroutil, Aashrita Rajagopalan, Markus Schober, Harald Pichler, Karl Gruber, Frank Niehaus, Silvia M. Glueck, Anna Migglautsch
Publikováno v:
ChemBioChem. 14:2427-2430
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 90:118-122
Alkene cleavage is a widely employed oxidation reaction in organic chemistry. An enzyme preparation of the wood degrading fungus Trametes hirsuta is known to cleave the C C double bond adjacent to an aromatic ring to give the corresponding carbonyl c
Publikováno v:
Advanced Synthesis & Catalysis. 352:731-736
The chemical synthesis of 3-substituted tyrosine derivatives requires a minimum of four steps to access optically enriched material starting from commercial precursors. Attempting to short-cut the cumbersome chemical synthesis of 3-substituted tyrosi
Publikováno v:
ChemCatChem. 2:73-77
Various recombinant ω-transaminases, overexpressed in E. coli cells and employed as whole-cell catalysts, are tested for the synthesis of enantiomerically pure amines from the corresponding prochiral ketones. Optically pure (S)-amines are obtained b
Publikováno v:
European Journal of Organic Chemistry. 2009:2293-2298
A three-step, two-enzyme, one-pot reaction sequence starting from prochiral α-chloroketones leading to enantiopure β-azidoalcohols and β-hydroxynitriles is described. Asymmetric bioreduction of α-chloroketones by hydrogen transfer catalysed by an
Autor:
Joerg H. Schrittwieser, Iván Lavandera, Wolfgang Kroutil, Barbara Mautner, Jeffrey H. Lutje Spelberg, Birgit Seisser
Publikováno v:
Tetrahedron: Asymmetry. 20:483-488
Hydroxide-loaded anion exchangers have been successfully employed to shift the equilibrium of a one-pot, two-step, two-enzyme cascade reaction affording enantiopure epoxides starting from prochiral α-chloroketones. The α-chloroketones were asymmetr
Publikováno v:
Advanced Synthesis & Catalysis. 349:1399-1404
A novel one-pot, two-step, two-enzyme cascade is described. Pro-chiral α-chloro ketones are stereoselectively reduced to the corresponding halohydrins as an intermediate by a biocatalytic hydrogen transfer process. The intermediate is transformed to
Autor:
Kurt Faber, Andreas Hafner, Wolfgang Kroutil, Sandra F. Mayer, Klaus Edegger, Wolfgang Stampfer, Reinhold Oehrlein, Birgit Seisser
Publikováno v:
European Journal of Organic Chemistry. 2006:1904-1909
The asymmetric reduction of symmetrical and nonsymmetrical diketones as well as the stereoselective oxidation of various diols by biocatalytic hydrogen transfer was investigated by employing lyophilized cells of Rhodococcus ruber DSM 44541 containing
Autor:
Alessandra Bonamore, Alberto Macone, Wolfgang Kroutil, Birgit Seisser, Tijs M. Lammens, Daniela De Biase, Maurice C. R. Franssen, Elinor L. Scott, Johan P. M. Sanders, Kenji Miyamoto, Robert Kourist, Shosuke Yoshida, Hiromichi Ohta, Jie Tian, Heng Li, Wen‐Yun Gao, Saravanakumar Shanmuganathan, Dessy Natalia, Lasse Greiner, Pablo Domínguez de María, Yan‐Hong He, Zhi Guan, Jian‐Feng Cai
Publikováno v:
Practical Methods for Biocatalysis and Biotransformations 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b66e981a5117b69cadd1cbd491766d
http://hdl.handle.net/11573/508757
http://hdl.handle.net/11573/508757
Publikováno v:
Enzyme Technologies: Metagenomics, Evolution, Biocatalysis, and Biosynthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9e761cca76da0df99f24e47181bb780
https://doi.org/10.1002/9780470627303.ch7
https://doi.org/10.1002/9780470627303.ch7