@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}
}
@article{SchmidtHoelter2009,
  author    = {Schmidt, Bernd and Hoelter, Frank},
  title     = {A stereodivergent synthesis of all stereoisomers of centrolobine : control of selectivity by a protecting-group manipulation},
  issn      = {0947-6539},
  doi       = {10.1002/chem.200902053},
  year      = {2009},
  abstract  = {All stereoisomers of the natural product centrolobine are selectively synthesized, by starting from a common precursor. Key steps are an enantioselective allylation with enantiomerically pure allylsilanes, a tandem ring-closing metathesis-isomerization reaction, and a Heck reaction by using an arene diazonium salt. By choosing appropriate conditions for the final deprotection step, either the cis-configured centrolobines or their epimers are selectively obtained.},
  language  = {en}
}