@article{SchmidtBerger2013,
  author    = {Schmidt, Bernd and Berger, Ren{\´e}},
  title     = {A deacetylation-diazotation-coupling sequence - palladium-catalyzed CC bond formation with acetanilides as formal leaving groups},
  series = {Advanced synthesis \& catalysis},
  volume    = {355},
  journal   = {Advanced synthesis \& catalysis},
  number    = {2-3},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1615-4150},
  doi       = {10.1002/adsc.201200929},
  pages     = {463 -- 476},
  year      = {2013},
  abstract  = {Acetanilides can be deacetylated and diazotized in situ, and subsequently used in Pd-catalyzed coupling reactions without isolation of the diazonium intermediate. Heck reactions, Suzuki cross-coupling reactions, and a Pd-catalyzed [2+2+1]cycloaddition have been investigated as terminating CC bond-forming steps of this one-flask sequence. The sequence does not require the exchange of solvents or removal of by-products between the individual steps, but proceeds by addition of reagents and catalysts in due course.},
  language  = {en}
}