@article{SchultzeFossSchmidt2020,
  author    = {Schultze, Christiane and Foß, Stefan and Schmidt, Bernd},
  title     = {8-Prenylflavanones through microwave promoted tandem claisen rearrangement/6-endo-trig cyclization and cross metathesis},
  series = {European journal of organic chemistry},
  volume    = {2020},
  journal   = {European journal of organic chemistry},
  number    = {47},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1434-193X},
  doi       = {10.1002/ejoc.202001378},
  pages     = {7373 -- 7384},
  year      = {2020},
  abstract  = {Prenylated flavanones were obtained from ortho-allyloxy chalcones through a one-pot sequence of Claisen rearrangement and 6-endo-trig cyclization, followed by olefin cross metathesis of the intermediate allyl flavanones with 2-methyl-2-butene. The synthetic utility of this route is illustrated for the synthesis of several naturally occurring prenyl flavanones.},
  language  = {en}
}