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An attempted synthesis of naphtho [ghij] pleiadene

dc.contributor.authorStacey, Jennifer Lynne
dc.date.accessioned2011-03-15T22:51:04Z
dc.date.accessioned2022-10-25T05:34:19Z
dc.date.available2011-03-15T22:51:04Z
dc.date.available2022-10-25T05:34:19Z
dc.date.copyright1972
dc.date.issued1972
dc.description.abstractMany studies, both theoretical and practical, have been made of compounds containing a seven-membered ring with aromatic rings fused around it. Pullman et al Pullman, B., Pullman, A., Berthier, G., Pontis, J., J. Chim. Phys. 1952, 49, 20. made a theoretical study of pleiadiene (I), acepleiadylene (II), pleiadene (III) and benzo[4, 5] cyclohepta[l,2,3-de] naphthalene (IV). Pleiadiene (I) and acepleiadylene (II), which were synthesysed by Boekelheide and Vick Boekelheide, V., Vick, G.K., J. Am. Chem. Soc., 1956, 78, 653. were found to have physical and chemical properties which agreed with those predicted by calculation. In 1963, Cava and Schlessinger Cava, M.P., Schlessinger, R.H., J. Am. Chem. Soc., 1963, 85, 835 described an attempted synthesis of pleiadene (III) and its acenaphthalene analogue (V). They found, however, that these were much less stable than pleiadiene (I) or acepleiadylene (II). Neither compound could be isolated except as the dimer resulting from Diels-Alder self-condensation.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/23305
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.subjectAromatic compounds
dc.subjectOrganic compounds synthesis
dc.subjectChemistry
dc.titleAn attempted synthesis of naphtho [ghij] pleiadeneen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineChemistryen_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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