B
Burkhard König
Researcher at University of Regensburg
Publications - 568
Citations - 27308
Burkhard König is an academic researcher from University of Regensburg. The author has contributed to research in topics: Catalysis & Photoredox catalysis. The author has an hindex of 73, co-authored 562 publications receiving 22098 citations. Previous affiliations of Burkhard König include University of Bordeaux & University of Kansas.
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Journal ArticleDOI
Palladium-Catalyzed Additions of Alkenyl Epoxides to Pronucleophiles: A Synthesis of the Macrolactam Aglycone of Fluviricin B1
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NADH model systems functionalized with Zn(II)-cyclen as flavin binding site-structure dependence of the redox reaction within reversible aggregates.
TL;DR: A strong dependence of the reaction rate on the spacer length was observed, which clearly shows that within the dynamic reversible assembly only the optimal relative disposition of the redox partners ensures an efficient redox reaction.
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Visible-Light-Mediated Photoredox-Catalyzed N-Arylation of NH-Sulfoximines with Electron-Rich Arenes.
Alexander Wimmer,Burkhard König +1 more
TL;DR: This work proposes a radical‐based mechanism, where both the arene and the NH‐sulfoximine are photo‐oxidized to their respective radical intermediates, and radical‐radical cross‐coupling subsequently leads to the N‐arylated sulfoximines.
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Azo pigments and a basal cell carcinoma at the thumb.
Eva Engel,Heidi Ulrich,Rudolf Vasold,Burkhard König,Michael Landthaler,Rudolf Süttinger,Wolfgang Bäumler +6 more
TL;DR: The case of a 58-year-old patient with a periungual basal cell carcinoma at the thumb is reported, and the frequent exposure to fishing baits that the patient had stained with an unknown colorant is revealed as the azo pigment Solvent Red 8.
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Two-Acceptor Cyanine-Based Fluorescent Indicator for NAD(P)H in Tumor Cell Models
Maksim A. Fomin,Maksim A. Fomin,Ruslan I. Dmitriev,James Jenkins,Dmitri B. Papkovsky,Dieter Heindl,Burkhard König +6 more
TL;DR: A small molecule indicator, which allows both colorimetric and fluorescent NAD(P)H detection in biological samples and is based on a cyanine dye scaffold and utilizes a novel two-acceptor “turn-on” mechanism, which features unprecedented sensitivity and rapid response toward NAD( P)H at low micromolar levels under physiological conditions.