@article{BudimanWestcottRadiusetal.2021,
  author    = {Budiman, Yudha P. and Westcott, Stephen A. and Radius, Udo and Marder, Todd B.},
  title     = {Fluorinated Aryl Boronates as Building Blocks in Organic Synthesis},
  series = {Advanced Synthesis \& Catalysis},
  volume    = {363},
  journal   = {Advanced Synthesis \& Catalysis},
  number    = {9},
  doi       = {10.1002/adsc.202001291},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-225908},
  pages     = {2224 -- 2255},
  year      = {2021},
  abstract  = {Organoboron compounds are well known building blocks for many organic reactions. However, under basic conditions, polyfluorinated aryl boronic acid derivatives suffer from instability issues that are accelerated in compounds containing an ortho-fluorine group, which result in the formation of the corresponding protodeboronation products. Therefore, a considerable amount of research has focused on novel methodologies to synthesize these valuable compounds while avoiding the protodeboronation issue. This review summarizes the latest developments in the synthesis of fluorinated aryl boronic acid derivatives and their applications in cross-coupling reactions and other transformations. image},
  language  = {en}
}
@article{BudimanFriedrichRadiusetal.2019,
  author    = {Budiman, Yudha P. and Friedrich, Alexandra and Radius, Udo and Marder, Todd B.},
  title     = {Copper-catalysed Suzuki-Miyaura cross-coupling of highly fluorinated aryl boronate esters with aryl iodides and bromides and fluoroarene-arene π-stacking interactions in the products},
  series = {ChemCatChem},
  volume    = {11},
  journal   = {ChemCatChem},
  number    = {21},
  doi       = {10.1002/cctc.201901220},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-204839},
  pages     = {5387-5396},
  year      = {2019},
  abstract  = {A combination of copper iodide and phenanthroline as the ligand is an efficient catalyst for Suzuki-Miyaura cross-coupling of highly fluorinated boronate esters (aryl-Bpin) with aryl iodides and bromides to generate fluorinated biaryls in good to excellent yields. This method represents a nice alternative to traditional cross-coupling methods which require palladium catalysts and stoichiometric amounts of silver oxide. We note that π⋅⋅⋅π stacking interactions dominate the molecular packing in the partly fluorinated biaryl crystals investigated herein. They are present either between the arene and perfluoroarene, or solely between arenes or perfluoroarenes, respectively.},
  language  = {en}
}