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@ARTICLE{Worgull:841836,
      author       = {Worgull, Dennis and Öhler, Laura and Strache, Joss Pepe
                      and Friedrichs, Teresa and Ullrich, Patrick},
      title        = {{E}nantioselective {S}ynthesis of 2,3-{D}ihydrofurans via
                      {A}mmonium {Y}lides},
      journal      = {European journal of organic chemistry},
      volume       = {2017},
      number       = {40},
      issn         = {1434-193X},
      address      = {Weinheim},
      publisher    = {Wiley-VCH Verl.},
      reportid     = {FZJ-2018-00137},
      pages        = {6077 - 6080},
      year         = {2017},
      abstract     = {A chiral, ammonium ylide based access to tetrasubstituted
                      2,3-dihydrofurans starting from readily available
                      benzylidene dicarbonyls and bromo acetophenones has been
                      developed. The products are obtained in moderate to good
                      yields with excellent diasteroselectivity and good to
                      excellent enantioselectivity (up to 99:1 e.r.). The employed
                      chiral amine can be recovered in near quantitative yield.
                      The transformation can be run as a three-component one-pot
                      reaction, generating the ammonium salt and ylide in situ.
                      The scope of this reaction includes 17 new dihydrofurans
                      with aromatic or heteroaromatic substituents.},
      cin          = {IBOC / IBG-1},
      ddc          = {540},
      cid          = {I:(DE-Juel1)IBOC-20090406 / I:(DE-Juel1)IBG-1-20101118},
      pnm          = {581 - Biotechnology (POF3-581)},
      pid          = {G:(DE-HGF)POF3-581},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000414341700015},
      doi          = {10.1002/ejoc.201701176},
      url          = {https://juser.fz-juelich.de/record/841836},
}