@article{SchmidtElizarovRiemeretal.2015,
  author    = {Schmidt, Bernd and Elizarov, Nelli and Riemer, Nastja and H{\"o}lter, Frank},
  title     = {Acetamidoarenediazonium Salts: Opportunities for Multiple Arene Functionalization},
  series = {European journal of organic chemistry},
  journal   = {European journal of organic chemistry},
  number    = {26},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1434-193X},
  doi       = {10.1002/ejoc.201500795},
  pages     = {5826 -- 5841},
  year      = {2015},
  abstract  = {Unlike their ortho counterparts, meta- and para-acetamidoanilines can be converted into the corresponding acetamidoarenediazonium salts. These offer various opportunities for multiple Pd-catalyzed arene functionalization reactions, such as Matsuda-Heck-, Suzuki-Miyaura- or Fujiwara-Moritani couplings.},
  language  = {en}
}
@article{SchmidtRiemer2015,
  author    = {Schmidt, Bernd and Riemer, Martin},
  title     = {Synthesis of Magnaldehydes B and E and Dictyobiphenyl B by Microwave-Promoted Cross-Coupling of Boronophenols},
  series = {European journal of organic chemistry},
  journal   = {European journal of organic chemistry},
  number    = {17},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1434-193X},
  doi       = {10.1002/ejoc.201500350},
  pages     = {3760 -- 3766},
  year      = {2015},
  abstract  = {Magnaldehydes B and E along with their 4'-methylated derivatives are naturally occurring 2,4'-biphenols that have been isolated from the Magnoliaceae. Herein, these natural products have been synthesized from a common intermediate, which was obtained by a microwave-promoted, hetero-geneously catalyzed, and protecting-group-free Suzuki-Miyaura coupling reaction in an aqueous medium. These reaction conditions were also successfully applied to a one-step synthesis of the slime mold metabolite dictyobiphenyl B.},
  language  = {en}
}