@article{SchreckChristl1987,
  author    = {Schreck, Michael and Christl, Manfred},
  title     = {Freisetzung und Abfangreaktionen von 1-Oxa-3,4-cyclohexadien},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-31597},
  year      = {1987},
  abstract  = {No abstract available},
  subject      = {Chemie},
  language  = {de}
}
@article{ChristlKrimmKraft1990,
  author    = {Christl, Manfred and Krimm, Stefan and Kraft, Arno},
  title     = {Einige Valene von benzanellierten f{\"u}nfgliedrigen Heteroarenen - Synthesen und NMR-Spektren},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-31559},
  year      = {1990},
  abstract  = {No abstract available},
  language  = {de}
}
@article{ChristlRoberts1972,
  author    = {Christl, Manfred and Roberts, John D.},
  title     = {Carbon-13 Nuclear Magnetic Resonance Spectroscopy : Conformational Analysis of Methyl-Substituted Cycloheptanes, Cycloheptanols, and Cycloheptanones},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-41663},
  year      = {1972},
  abstract  = {The 130 chemical shifts were determined of the carbons in 12 cycloheptanes, 21 cycloheptanols, and 8 cycloheptanones. In some cyc1oheptanols and cyc1oheptanones, the assignments have been obtained unambiguously by the synthesis of deuterated derivatives and the use of paramagnetic-shift reagents. Substituent effects for the different types of groups have been calculated. The most informative data about the cyc10heptane conformations were provided by the relatively well understood I' effects. The results are generally in,good agreement with predictions based on the twist-chair form, which has been predicted by Hendrickson to be the most stable conformation. Pairs of cis-trans isomers are found to have rather characteristic differences in their 130 spectra. This fact was used to assign the resonances found for cis-trans mixtures of methyl-substituted cyc1oheptanols to specific isomers.},
  language  = {en}
}
@article{ChristlLechner1975,
  author    = {Christl, Manfred and Lechner, M.},
  title     = {Zur intramolekularen Wechselwirkung von Cyclopropylidenen mit dem Bicyclo[1.1.0]butansystem},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-41509},
  year      = {1975},
  abstract  = {No abstract available},
  language  = {de}
}
@article{ChristlLanzendoerferFreund1981,
  author    = {Christl, Manfred and Lanzend{\"o}rfer, Ulrike and Freund, Silke},
  title     = {Olefinadditionen an 2,5-Diphenyl-1,3,4-oxadiazin-6-on},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-41525},
  year      = {1981},
  abstract  = {No abstract available},
  language  = {de}
}
@article{ChristlLessMueller1994,
  author    = {Christl, Manfred and Leß, Roland and M{\"u}ller, Heinrich},
  title     = {6,7-Dimethylene-2,4-diphenylbicyclo[3.2.l]oct-3-en-2-yl Anion : A Test for the Origin of the Unusual Properties of the Bicyclo[3.2.l]octa-3,6-dien-2-yl Anion},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-31547},
  year      = {1994},
  abstract  = {No abstract available},
  language  = {en}
}
@article{GigstadRicciJRMarkgrafetal.1991,
  author    = {Gigstad, Kenneth M. and Ricci JR., John S. and Markgraf, J. Hodge and Christl, Manfred and Kraft, Arno},
  title     = {Strained Heterocyclic Systems : 18. Structure of 1,2,3-Methylidyne-2,3-dihydro-1H-cyclopenta[b]quinoxaline},
  isbn      = {0108-2701},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-41645},
  year      = {1991},
  abstract  = {No abstract available},
  language  = {en}
}
@article{IrngartingerReimannLangetal.1990,
  author    = {Irngartinger, H. and Reimann, W. and Lang, R. and Christl, Manfred},
  title     = {Electron Density Distribution in a Bicyclo[l.l.0]butane},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-31576},
  year      = {1990},
  abstract  = {No abstract available},
  language  = {en}
}
@article{ChristlLeiningerMattauch1983,
  author    = {Christl, Manfred and Leininger, Hartmut and Mattauch, Brigitte},
  title     = {The <sup>13</sup>C NMR Spectra of Some Tricyclo[2.2.0.0<sup>2,6</sup>]hexane Derivatives : Unexpected High Field Absorptions Due to Additive gamma-anti Subsituent Effects},
  isbn      = {x},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-41620},
  year      = {1983},
  abstract  = {By means of the BC NMR spectra of tricyclo{2.2.0~rfJ6Jhexane and thirteen of its derivatives the effects of substituents in endo-3- and endo-5-positions on the HC chemical shifts have been determined. The y-anti effects are at least as Jarge as in monosubstituted cyc1obutanes, where the shielding values of second-row hetero substituents exceed those in unstrained systems by far, and higher-row and carbon substituents still cause substantial upfield shifts. In the title system the y-anti effect of a substituent in the endo-3- and endo-5-position are operative additively, and thus shift the absorption of C-J upfieJd by a maximum of 27 ppm with respect to the unsubstituted hydrocarbon.},
  language  = {en}
}
@article{HegmannChristlPetersetal.1988,
  author    = {Hegmann, Joachim and Christl, Manfred and Peters, Karl and Peters, Eva-Maria and Schnering, Hans Georg},
  title     = {Conjugated and Nonconjugated Cyclopentenones by a Reaction Cascade from Methyl 6-0xo-5-phenyl-1,3,4-oxadiazine-2-carboxylate and 1,3-Butadienes},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-30207},
  year      = {1988},
  abstract  = {No abstract available},
  language  = {en}
}