@article{SchmidtSchultze2018,
  author    = {Schmidt, Bernd and Schultze, Christiane},
  title     = {A one-pot synthesis of pyranocoumarins through microwave-promoted propargyl claisen rearrangement/wittig olefination},
  series = {European journal of organic chemistry},
  volume    = {2018},
  journal   = {European journal of organic chemistry},
  number    = {2},
  publisher = {Wiley-VCH Verl.},
  address   = {Weinheim},
  issn      = {1434-193X},
  pages     = {223 -- 227},
  year      = {2018},
  abstract  = {The reaction between propargyl ethers of hydroxybenzaldehydes and the ylide ethyl (triphenylphosphoranylidene)acetate was carried out under microwave irradiation to regioselectively afford angular pyranocoumarins. The chromene and coumarin heterocyclic scaffolds were simultaneously formed in the same synthetic step without changing the reaction conditions. The natural products seselin, braylin, and dipetalolactone were among the products synthesized by this method.},
  language  = {en}
}