@article{SchmidtHauke2014,
  author    = {Schmidt, Bernd and Hauke, Sylvia},
  title     = {Olefin cross metathesis based de novo synthesis of a partially protected L-amicetose and a fully protected L-cinerulose derivative},
  series = {Beilstein journal of organic chemistry},
  volume    = {10},
  journal   = {Beilstein journal of organic chemistry},
  publisher = {Beilstein-Institut zur F{\"o}rderung der Chemischen Wissenschaften},
  address   = {Frankfurt, Main},
  issn      = {1860-5397},
  doi       = {10.3762/bjoc.10.102},
  pages     = {1023 -- 1031},
  year      = {2014},
  abstract  = {Cross metathesis of a lactate derived allylic alcohol and acrolein is the entry point to a de novo synthesis of 4-benzoate protected L-amicetose and a cinerulose derivative protected at C5 and C1.},
  language  = {en}
}
@article{SchmidtHaukeMuehlenberg2014,
  author    = {Schmidt, Bernd and Hauke, Sylvia and Muehlenberg, Nino},
  title     = {Imino glycals via Ruthenium-catalyzed RCM and isomerization},
  series = {Synthesis},
  volume    = {46},
  journal   = {Synthesis},
  number    = {12},
  publisher = {Thieme},
  address   = {Stuttgart},
  issn      = {0039-7881},
  doi       = {10.1055/s-0033-1338615},
  pages     = {1648 -- 1658},
  year      = {2014},
  abstract  = {N-Allyl-N-homoallylamines were converted in one step into cyclic enamides via a ruthenium-catalyzed assisted tandem catalytic ring-closing metathesis-isomerization sequence. The sequence relies on the in situ transformation of a metathesis active Ru-carbene into an isomerization active Ru-hydride by addition of hydroxide as a chemical trigger.},
  language  = {en}
}