@article{SchmidtRiemerSchilde2014,
  author    = {Schmidt, Bernd and Riemer, Martin and Schilde, Uwe},
  title     = {Chroman-4-ones via microwave-promoted domino claisen rearrangement-oxa-michael addition: Synthesis of tabchromones A and B},
  series = {Synlett : accounts and rapid communications in synthetic organic chemistry},
  volume    = {25},
  journal   = {Synlett : accounts and rapid communications in synthetic organic chemistry},
  number    = {20},
  publisher = {Thieme},
  address   = {Stuttgart},
  issn      = {0936-5214},
  doi       = {10.1055/s-0034-1379364},
  pages     = {2943 -- 2946},
  year      = {2014},
  abstract  = {Allyl phenyl ethers with a pendant enone substituent undergo, upon microwave irradiation, a domino sequence of Claisen rearrangement and 6-endo-trig-cyclization to furnish functionalized chroman-4-ones. The natural products tabchromones A and B were synthesized via this method.},
  language  = {en}
}