@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}
}