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@PHDTHESIS{Hristeva:571844,
      author       = {Hristeva, Stanimira},
      othercontributors = {Enders, Dieter and Albrecht, Markus},
      title        = {{D}evelopment of new asymmetric organocatalytic domino
                      reactions for the synthesis of (benzo-fused) five- and
                      benzo-fused six-membered cyclic compounds},
      school       = {RWTH Aachen},
      type         = {Dissertation},
      address      = {Aachen},
      reportid     = {RWTH-2016-02350},
      pages        = {135 Seiten : Illustrationen},
      year         = {2015},
      note         = {Veröffentlicht auf dem Publikationsserver der RWTH Aachen
                      University; Dissertation, RWTH Aachen, 2015},
      abstract     = {The present dissertation reports the work performed in the
                      field of organocatalyzed domino reactions. The work can be
                      divided into four projects. The first project included the
                      development of a Michael/Michael domino reaction for the
                      construction of polysubstituted
                      1,2,3,4-tetrahydronaphthalenes through the reaction between
                      2-(nitromethyl)nitrostyrene and α,β-unsaturated aldehydes
                      successfully promoted by TMS-protected diphenylprolinol. In
                      the second project a new asymmetric organocatalyzed domino
                      reaction for the construction of 4,5-disubstituted
                      3-hydroxy-1H-pyrrol-2(5H)-ones was developed. The Brønsted
                      base cupreine successfully facilitated the
                      Mannich/cyclization cascade sequence between α-ketoesters
                      and aldimines. Next, the reaction between the
                      o-divinylketone and 3-phenylpropanal in conditions of
                      secondary amine organocatalysis was investigated. In the
                      last project, an enantioselective organocatalytic
                      Friedel-Crafts-type Michael addition of electron-rich arenes
                      to nitroolefins was studied.},
      cin          = {152110 / 150000},
      ddc          = {540},
      cid          = {$I:(DE-82)152110_20140620$ / $I:(DE-82)150000_20140620$},
      typ          = {PUB:(DE-HGF)11},
      urn          = {urn:nbn:de:hbz:82-rwth-2016-023506},
      doi          = {10.18154/RWTH-2016-02350},
      url          = {https://publications.rwth-aachen.de/record/571844},
}