@article{SchmidtElizarovBergeretal.2013,
  author    = {Schmidt, Bernd and Elizarov, Nelli and Berger, Ren{\´e} and Hoelter, Frank},
  title     = {Scope and limitations of the Heck-Matsuda-coupling of phenol diazonium salts and styrenes a protecting-group economic synthesis of phenolic stilbenes},
  series = {Organic \& biomolecular chemistry : an international journal of synthetic, physical and biomolecular organic chemistry},
  volume    = {11},
  journal   = {Organic \& biomolecular chemistry : an international journal of synthetic, physical and biomolecular organic chemistry},
  number    = {22},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1477-0520},
  doi       = {10.1039/c3ob40420j},
  pages     = {3674 -- 3691},
  year      = {2013},
  abstract  = {4-Phenol diazonium salts undergo Pd-catalyzed Heck reactions with various styrenes to 4'-hydroxy stilbenes. In almost all cases higher yields and fewer side products were observed, compared to the analogous 4-methoxy benzene diazonium salts. In contrast, the reaction fails completely with 2- and 3-phenol diazonium salts. For these substitution patterns the methoxy-substituted derivatives are superior.},
  language  = {en}
}
@misc{SchmidtElizarovBergeretal.2013,
  author    = {Schmidt, Bernd and Elizarov, Nelli and Berger, Ren{\´e} and H{\"o}lter, Frank},
  title     = {Scope and limitations of the Heck-Matsuda-coupling of phenol diazonium salts and styrenes},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-95070},
  pages     = {3674 -- 3691},
  year      = {2013},
  abstract  = {4-Phenol diazonium salts undergo Pd-catalyzed Heck reactions with various styrenes to 4'-hydroxy stilbenes. In almost all cases higher yields and fewer side products were observed, compared to the analogous 4-methoxy benzene diazonium salts. In contrast, the reaction fails completely with 2- and 3-phenol diazonium salts. For these substitution patterns the methoxy-substituted derivatives are superior.},
  language  = {en}
}
@article{SchmidtElizarovBergeretal.2013,
  author    = {Schmidt, Bernd and Elizarov, Nelli and Berger, Ren{\´e} and Petersen, Monib H.},
  title     = {From paracetamol to rolipram and derivatives - application of deacetylation-diazotation sequences and palladium-catalyzed matsuda-heck reaction},
  series = {Synthesis},
  volume    = {45},
  journal   = {Synthesis},
  number    = {9},
  publisher = {Thieme},
  address   = {Stuttgart},
  issn      = {0039-7881},
  doi       = {10.1055/s-0032-1316874},
  pages     = {1174 -- 1180},
  year      = {2013},
  abstract  = {A six-step synthesis of the antidepressant rolipram from the popular analgetic 4-acetamidophenol (paracetamol) is described. The steps include oxidative functionalization of the aromatic core, diazonium salt formation via deacetylation-diazotation, Matsuda-Heck reaction, conjugate addition of nitromethane, and hydrogenative cyclization.},
  language  = {en}
}