@article{WessigBadetkoCzarneckietal.2022,
  author    = {Wessig, Pablo and Badetko, Dominik and Czarnecki, Maciej and Wichterich, Lukas and Schmidt, Peter and Brudy, Cosima and Sperlich, Eric and Kelling, Alexandra},
  title     = {Studies toward the total synthesis of arylnaphthalene lignans via a Photo-Dehydro-Diels-Alder (PDDA) reaction},
  series = {The journal of organic chemistry},
  volume    = {87},
  journal   = {The journal of organic chemistry},
  number    = {9},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0022-3263},
  doi       = {10.1021/acs.joc.2c00195},
  pages     = {5904 -- 5915},
  year      = {2022},
  abstract  = {An efficient method for the preparation of arylnaphthalene lignans (ANLs) was developed, which is based on thePhoto-Dehydro-DIELS-ALDER(PDDA) reaction. While intermolecular PDDA reactions turned out to be inefficient, theintramolecular variant using suberic acid as tether linking two aryl propiolic esters smoothly provided naphthalenophanes. Theirradiations were performed with a previously developed annular continuous-flow reactor and UVB lamps. In this way, the naturalproducts Alashinol D, Taiwanin C, and an unnamed ANL could be prepared.},
  language  = {en}
}