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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Developing and Disseminating NOP: An Online, Open-Access, Organic Chemistry Teaching Resource To Integrate Sustainability Concepts in the Laboratory.
TL;DR: The NOP resource as mentioned in this paper includes additional parameters that should be considered in the organic chemistry laboratory: atom economy of chemical transformations, energy efficiency of chemical transformation, questions of waste; renewable feedstocks; toxicity and ecotoxicity; and safety measures for the chemicals used.
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Detection of protein phosphorylation on SDS-PAGE using probes with a phosphate-sensitive emission response.
TL;DR: Fluorescent probes for the detection of protein phosphorylation on SDS-PAGE are presented, designed using a dinuclear metal-chelate phosphate recognition unit and an environmentally sensitive fluorophore.
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Minisci C-H Alkylation of Heteroarenes Enabled by Dual Photoredox/Bromide Catalysis in Micellar Solutions*.
TL;DR: This work describes a photocatalytic Minisci-type C-H functionalization of heteroarenes with non-activated alkyl bromides with critical importance of microstructuring and organization of the components in the reaction mixture.
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Metal-catalyzed derivatization of C(alpha)-tetrasubstituted amino acids and their use in the synthesis of cyclic peptides.
TL;DR: This work reports on the functionalization of the C(alpha)-tetrasubstituted THF amino acid rac-5 by copper(I) catalyzed N-arylation reactions, which replaces the aryl bromide substituent with a variety of aliphatic and aromatic amines.
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Chemical Photocatalysis with Rhodamine 6G: Investigation of Photoreduction by Simultaneous Fluorescence Correlation Spectroscopy and Fluorescence Lifetime Measurements.
TL;DR: The formation and lifetime of the rhodamine 6G (Rh6G) radical anion can be followed in detail by single-molecule fluorescence correlation spectroscopy combined with simultaneous fluorescence lifetime measurements, and the results provide a guideline toward generating an increased yield of radical anions of the dye under photoexcitation.