Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Anett Schallmey"'
Publikováno v:
Biosensors, Vol 11, Iss 11, p 407 (2021)
This Perspective discusses the literature related to two-phase biocatalysis in microfluidic droplets. Enzymes used as catalysts in biocatalysis are generally less stable in organic media than in their native aqueous environments; however, chemical an
Externí odkaz:
https://doaj.org/article/bd9d502cd34142598f450fd924f6569a
Publikováno v:
Crystals, Vol 11, Iss 7, p 718 (2021)
Enzymes are able to catalyze various specific reactions under mild conditions and can, therefore, be applied in industrial processes. To ensure process profitability, the enzymes must be reusable while ensuring their enzymatic activity. To improve th
Externí odkaz:
https://doaj.org/article/9754f7687a0f49f9841743704fe12b15
Autor:
Martin Empting, Volkmar Braun, Dieter Jahn, Mathias Hornef, Daniela Kruck, Jürgen Lassak, Johannes Sander, Anett Schallmey, Daniel B. Eckl
Publikováno v:
BIOspektrum. 29:166-171
Publikováno v:
Catalysis Research. :1-12
A two-step protocol for the synthesis of aryl-3-hydroxypropanones, which were regarded as lignin degradation products, was proposed herein. This protocol provided a more rapid and easier access to aryl-3-hydroxypropanones, and aryl-3-hydroxypropanone
Publikováno v:
Analytical Chemistry. 94:8132-8135
This report advises against the use of 5-iodoridine or 5-ethynyluridine as alternative assay reagents in the PUB module, primarily due to their lack of an isosbestic point of phosphorolysis under moderately alkaline conditions.
Autor:
Felix Kaspar, Felix Brandt, Sarah Westarp, Lea Eilert, Sebastian Kemper, Anke Kurreck, Peter Neubauer, Christoph R. Jacob, Anett Schallmey
Publikováno v:
Angewandte Chemie International Edition. 62
Biocatalytic nucleoside (trans-)glycosylations catalyzed by nucleoside phosphorylases have graduated to a practical and convenient approach to the preparation of modified nucleosides, which are important pharmaceuticals for the treatment of various c
Autor:
Anna P. Lehmann, Christoph Köllmann, Anett Schallmey, Anke Kurreck, Patrick Pausch, Felix Kaspar, Peter Neubauer, Gert Bange, Daniel B. Werz, Margarita Seeger, Sebastian Kemper, Sarah Westarp
Publikováno v:
ACS Catalysis. 11:10830-10835
The growing demand for 4'-modified nucleoside analogs in medicinal and biological chemistry is contrasted by the challenging synthetic access to these molecules and the lack of efficient diversification strategies. Herein, we report the development o
Autor:
Francesco Mascia, Sara B. Pereira, Catarina C. Pacheco, Paulo Oliveira, Jennifer Solarczek, Anett Schallmey, Robert Kourist, Véronique Alphand, Paula Tamagnini
Publikováno v:
Green Chemistry
Green Chemistry, Royal Society of Chemistry, 2022, 24 (16), pp.6156-6167. ⟨10.1039/d1gc04714k⟩
Green Chemistry, 2022, 24 (16), pp.6156-6167. ⟨10.1039/d1gc04714k⟩
Green Chemistry, Royal Society of Chemistry, 2022, 24 (16), pp.6156-6167. ⟨10.1039/d1gc04714k⟩
Green Chemistry, 2022, 24 (16), pp.6156-6167. ⟨10.1039/d1gc04714k⟩
International audience; The selective hydroxylation of steroids through chemical synthesis is a complex reaction with a high environmental impact. The use of photoautotrophic microorganisms expressing heterologous monooxygenases could overcome this p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da44040efbf2e5c9c84be0e31beebd0
https://hal.archives-ouvertes.fr/hal-03784038
https://hal.archives-ouvertes.fr/hal-03784038
Halohydrin dehalogenases are promiscuous biocatalysts, which enable asymmetric ring opening reactions of epoxides with various anionic nucleophiles. However, despite the increasing interest in such asymmetric transformations, the substrate scope of G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4fa7c3e4cb85479d01f16e1521ca37b
https://doi.org/10.26434/chemrxiv-2022-jl3gd
https://doi.org/10.26434/chemrxiv-2022-jl3gd
Autor:
Philipp Süss, Maurice C. R. Franssen, Caroline E. Paul, Anett Schallmey, Lía Martínez-Montero, Dirk Tischler, Frank Hollmann
Publikováno v:
Catalysis science & technology : a multidisciplinary journal focussing on all fundamental science and technological aspects of catalysis, 2021, 11, 15, 5077 – 5085--Catal Sci Technol--2044-4753--2044-4761
Catalysis Science & Technology
Catalysis Science and Technology 11 (2021) 15
Catalysis Science and Technology, 11(15), 5077-5085
Catalysis Science & Technology, 11(15)
Catalysis Science & Technology
Catalysis Science and Technology 11 (2021) 15
Catalysis Science and Technology, 11(15), 5077-5085
Catalysis Science & Technology, 11(15)
Enantioenriched azido alcohols are precursors for valuable chiral aziridines and 1,2-amino alcohols, however their chiral substituted analogues are difficult to access. We established a cascade for the asymmetric azidohydroxylation of styrene derivat