@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}
}
@article{SchmidtRiemerSchilde2015,
  author    = {Schmidt, Bernd and Riemer, Martin and Schilde, Uwe},
  title     = {Tandem Claisen Rearrangement/6-endo Cyclization Approach to Allylated and Prenylated Chromones},
  series = {European journal of organic chemistry},
  journal   = {European journal of organic chemistry},
  number    = {34},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1434-193X},
  doi       = {10.1002/ejoc.201501151},
  pages     = {7602 -- 7611},
  year      = {2015},
  abstract  = {Allyl, dimethylallyl and prenyl ethers derived from o-acyl-phenols reacted upon microwave irradiation to form C-allylated or -prenylated chromone derivatives, depending on the substitution pattern of the arene and the allyl substituent. The reaction proceeds through a tandem Claisen rearrangement and 6-endo-trig or 6-endo-dig cyclization sequence. For prenyl ethers, the tandem sequence can be extended by a Cope rearrangement to furnish 6-prenylchromones. The method is potentially useful for the synthesis of natural products and drugs.},
  language  = {en}
}