@article{LoodSchmidt2020,
  author    = {Lood, Kajsa and Schmidt, Bernd},
  title     = {Stereoselective synthesis of conjugated polyenes based on tethered olefin metathesis and carbonyl olefination},
  series = {The journal of organic chemistry},
  volume    = {85},
  journal   = {The journal of organic chemistry},
  number    = {7},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0022-3263},
  doi       = {10.1021/acs.joc.0c00446},
  pages     = {5122 -- 5130},
  year      = {2020},
  abstract  = {The combination of a highly stereoselective tethered olefin metathesis reaction and a Julia-Kocienski olefination is presented as a strategy for the synthesis of conjugated polyenes with at least one Z-configured C=C bond. The strategy is exemplified by the synthesis of the marine natural product (+)-bretonin B.},
  language  = {en}
}
@article{SchmidtRiemer2016,
  author    = {Schmidt, Bernd and Riemer, Martin},
  title     = {Synthesis of Allyl- and Prenylcoumarins via Microwave-Promoted Tandem Claisen Rearrangement/Wittig Olefination},
  series = {Synthesis},
  volume    = {48},
  journal   = {Synthesis},
  publisher = {Thieme},
  address   = {Stuttgart},
  issn      = {0039-7881},
  doi       = {10.1055/s-0035-1560501},
  pages     = {141 -- 149},
  year      = {2016},
  abstract  = {Allyl, dimethylallyl, crotyl, and prenyl ethers of various aromatic ortho-hydroxy carbonyl compounds undergo a tandem sequence of Claisen rearrangement, carbonyl olefination, and cyclization upon microwave irradiation in the presence of a stabilized ylide. The products are multiply substituted 6- or 8-allylated or prenylated coumarins (2H-chromen-2-ones).},
  language  = {en}
}