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An attempted synthesis of naphtho [ghij] pleiadene

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dc.contributor.author Stacey, Jennifer Lynne
dc.date.accessioned 2011-03-15T22:51:04Z
dc.date.accessioned 2022-10-25T05:34:19Z
dc.date.available 2011-03-15T22:51:04Z
dc.date.available 2022-10-25T05:34:19Z
dc.date.copyright 1972
dc.date.issued 1972
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/23305
dc.description.abstract Many 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.format pdf en_NZ
dc.language en_NZ
dc.language.iso en_NZ
dc.publisher Te Herenga Waka—Victoria University of Wellington en_NZ
dc.title An attempted synthesis of naphtho [ghij] pleiadene en_NZ
dc.type Text en_NZ
vuwschema.type.vuw Awarded Research Masters Thesis en_NZ
thesis.degree.discipline Chemistry en_NZ
thesis.degree.grantor Te Herenga Waka—Victoria University of Wellington en_NZ
thesis.degree.level Masters en_NZ
thesis.degree.name Master of Science en_NZ


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