[1]

  • K. Kolahdouzan, R. Khalaf, J.M. Grandner, Y. Chen, J.A. Terrett, and M.P. Huestis, "Dual Photoredox/Nickel-Catalyzed Conversion of Aryl Halides to Aryl Aminooxetanes: Computational Evidence for a Substrate-Dependent Switch in Mechanism", ACS Catalysis, vol. 10, pp. 405-411, 2019. http://dx.doi.org/10.1021/acscatal.9b03596
  • [1]

  • E.D. Kalkman, M.G. Mormino, and J.F. Hartwig, "Unusual Electronic Effects of Ancillary Ligands on the Perfluoroalkylation of Aryl Iodides and Bromides Mediated by Copper(I) Pentafluoroethyl Complexes of Substituted Bipyridines", Journal of the American Chemical Society, vol. 141, pp. 19458-19465, 2019. http://dx.doi.org/10.1021/jacs.9b10540
  • 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