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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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MonographDOI
Photocatalysis in Organic Synthesis
Burkhard König,Munetaka Akita,J. Albero,Adrian G. Amador,M. A. Ashley,Malte Brasholz,V. Corcé,D. A. DiRocco,S. Dix,P. Ehrnsberger,L. Fensterbank,F. Gaida,H. García,Indrajit Ghosh,Ryan Gilmour,Axel G. Griesbeck,Á. Gutiérrez Bonet,Hamish B. Hepburn,M. N. Hopkinson,C. B. Kelly,Takashi Koike,R. Laha,S. B. Lang,D. Leonori,C. Lévêque,P. Li,L.-Q. Lu,J. K. Matsui,Paolo Melchiorre,Jan B. Metternich,G. A. Molander,R. J. Mudd,C. Ollivier,G. Pandey,J. P. Phelan,Oliver Reiser,Yannick P. Rey,T. Rovis,A. Ruffoni,Spencer O. Scholz,Danielle M. Schultz,Kazimer L. Skubi,E. Speckmeier,S. M. Thullen,Moritz Vollmer,L. Wang,M. Wang,Y. Wei,W.-J. Xiao,Tehshik P. Yoon,Kirsten Zeitler,Q.-Q. Zhou +51 more
Journal ArticleDOI
Nitrosonium-Mediated Phenol–Arene Cross-Coupling Involving Direct C–H Activation
TL;DR: In this article, an environmentally benign and mild method for the in situ formation of NO+ from readily available inorganic nitrate salts, i.e., lithium nitrate, through a finely tuned interplay between formic acid and MeOH, which are used as the solvent system.
Journal ArticleDOI
2′-Oxoethyl Flavin Revisited
TL;DR: In this paper, the authors investigated the possibility of using 2'-oxoethyl flavin (2) as a starting material for the construction of more complicated flavin-based molecules, and they found an intramolecular hydrogen bond between one of the hydroxy groups of the diol and the N1 atom of the flavin skeleton.
Journal ArticleDOI
Synthesis and Photoisomerization of Diarylcyclobutenes
TL;DR: Symmetrically and unsymmetric substituted diarylcyclobutenes are synthesized in 20-70% yields from alkyne precursors via cobalt-catalyzed [2+2] cycloadditions as discussed by the authors.
Journal ArticleDOI
Synthesis of [2.2]paracyclophane annelated cycloproparenes
TL;DR: The [2.2]paracyclophane annelated cycloproparenes 2 and 3 were synthesized by dehydrohalogenation of the adducts prepared by reacting 1-bromo-2-chlorocyclopropene with 1-vinyl[2] paracyclogenes as discussed by the authors.