@book{OPUS4-20533,
  title     = {Einfache Experimente},
  editor    = {Duvinage, Brigitte},
  year      = {1999},
  language  = {de}
}
@book{OPUS4-27556,
  title     = {Chemie : Lehrbuch f{\"u}r die Sekundarstufe II ; Gymnasium/Gesamtschule ; Allgemeine Chemie, organische Chemie},
  editor    = {Barthel, Helmut and Henning, Helmut and Kleinpeter, Erich and Ludwig, Eberhard and Uhlemann, Erhard and Barthel, Helmut},
  publisher = {Volk und Wissen},
  address   = {Berlin},
  pages     = {224 S.},
  year      = {1995},
  language  = {de}
}
@book{OPUS4-27192,
  title     = {Chemie : Lehrbuch f{\"u}r die Sekundarstufe II ; Gymnasium/Gesamtschule ; Allgemeine Chemie, organische Chemie ; L{\"o}sungen},
  editor    = {Barthel, Helmut and Henning, Helmut and Kleinpeter, Erich and Ludwig, Eberhard and Uhlemann, Erhard and Barthel, Helmut},
  publisher = {Volk und Wissen},
  address   = {Berlin},
  pages     = {40 S.},
  year      = {1995},
  language  = {de}
}
@article{OPUS4-10587,
  title     = {DFT-GIAO-NBO and 13C NMR study of the delta-syn-axial effect in 2,4-disubstituted adamantanes},
  issn      = {0749-1581},
  doi       = {10.1002/Mrc.2333},
  year      = {2008},
  abstract  = {Six groups of diastereomeric 2,4-disubstituted adamantanes were studied with DFT-GIAO-NBO (natural orbital analysis) methods. The calculated 13C chemical shifts reproduce well the experimental data. It was found that among all diastereomers, those bearing substituents in -syn-axial positions showed the largest overall deshielding, i.e. the sum of all 13C chemical shifts [;;(13C)] was the greatest and also had the highest delocalization contribution to the molecular energy evaluated with NBO. The higher delocalization energy is proposed to be the origin of the deshielding -syn-axial effect},
  language  = {en}
}
@article{OPUS4-10769,
  title     = {Synthesis and conformational analysis of phenyl-substituted 1,3,2-oxazaphosphino[4,3-a]- and 1,2,3- oxathiazino[4,3-a]isoquinolines},
  year      = {2008},
  abstract  = {Through the ring closures of tetrahydroisoquinoline 1,3-amino alcohols bearing a phenyl group in the side- chain, diastereomers of novel 1- or 2-phenyl-substituted 1,3,2-oxazaphosphino[4,3-a]isoquinoline 4-oxides, and 1,2,3- oxathiazino[4,3-a]isoquinoline 4-oxides and 4,4-dioxides were prepared. NMR analysis and DFT calculations on the prepared tetrahydroisoquinoline-condensed 1,2,3-heterocycles revealed that their conformational equilibria of cis1-trans-cis2 type are influenced by the relative configuration of P-4 in the 1,3,2-oxazaphosphinanes, and by the position of the phenyl group in the 1,2,3-oxathiazines.},
  language  = {en}
}