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  • H. Huang, and T.H. Lambert, "Electrophotocatalytic SN Ar Reactions of Unactivated Aryl Fluorides at Ambient Temperature and Without Base", Angewandte Chemie International Edition, vol. 59, pp. 658-662, 2019. http://dx.doi.org/10.1002/anie.201909983
  • Very interesting solvent effect described by Schoenebeck, making it possible to selectively couple @ C-Br, then @ C-OSO2F, and finally @ C-Cl bonds on a range of substrates.
    [1]

  • M. Mendel, I. Kalvet, D. Hupperich, G. Magnin, and F. Schoenebeck, "Site-Selective, Modular Diversification of Polyhalogenated Aryl Fluorosulfates (ArOSO2 F) Enabled by an Air-Stable PdI Dimer", Angewandte Chemie International Edition, 2019. http://dx.doi.org/10.1002/anie.201911465
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  • L. Wortmann, B. Lindenthal, P. Muhn, A. Walter, R. Nubbemeyer, D. Heldmann, L. Sobek, F. Morandi, A.K. Schrey, D. Moosmayer, J. Günther, J. Kuhnke, M. Koppitz, U. Lücking, U. Röhn, M. Schäfer, K. Nowak-Reppel, R. Kühne, H. Weinmann, and G. Langer, "Discovery of BAY-298 and BAY-899: Tetrahydro-1,6-naphthyridine-Based, Potent, and Selective Antagonists of the Luteinizing Hormone Receptor Which Reduce Sex Hormone Levels in Vivo", Journal of Medicinal Chemistry, vol. 62, pp. 10321-10341, 2019. http://dx.doi.org/10.1021/acs.jmedchem.9b01382