Studies in synthesis and stereochemistry

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dc.contributor.advisor Davis, B.R. en
dc.contributor.advisor Woodgate, P.D. en
dc.contributor.author Johnson, Stephen Joseph en
dc.date.accessioned 2007-08-28T08:15:07Z en
dc.date.available 2007-08-28T08:15:07Z en
dc.date.issued 1983 en
dc.identifier THESIS 83-166 en
dc.identifier.citation Thesis (PhD--Chemistry)--University of Auckland, 1983 en
dc.identifier.uri http://hdl.handle.net/2292/1557 en
dc.description Full text is available to authenticated members of The University of Auckland only. en
dc.description.abstract The Lewis and protic acid catalysed dimerization of the 3-methyl-1H-inden-4-ol (3) in non-polar solvents leads to pentacyclic diindeno[7,1-b,c: 2',1'-e]pyrans. The reaction shows kinetic selectivity for the formation of "endo" product (4) while the "exo" dimer (5) is thermodynamically more stable. Under polar conditions, the acid catalysed reaction favours uncyclized diindene (6), while the 1H-indene-l,7-diol (2) affords unstable pentacyclic spiro dimers (29) and (30) merely on standing. When dissolved in trifluoroacetic acid, the dimers derived from indenol (3) dissociate to give the monomeric carbocation (63) which has been identified by n.m.r. spectroscopy. The indenol (14) dimerizes to give four stereoisomeric diindeno[7,1-bc: 2',1'-e]pyrans. Co-dimerization of certain methyl and butyl indenols afforded crossed-dimers which have been isolated by chromatography. Correlation of the n.m.r. spectra of these pentacyclic crossed-dimers with the spectra of dimers derived solely for indenol (3) or (4) allowed unequivocal assignment of most alkyl carbon and proton signals. The relative configuration and stereochemistry of each dimer has been deduced by detailed comparison of n.m.r. spectra and mass spectra. The dimerization of the 4-hydroxy-3-methyl-1H-inden-1-one (35) is less facile than that of the analogous indene (3), but the reaction shows similar kinetic preference for the formation of "endo" dimer (37) which is slightly less thermodynamically stable than "exo" dimer (56). These indenone dimers do not dissociate greatly in trifluoroacetic acid and equilibration is slow. Rapid opening of the pyran ring occurs in base and brief treatment of indenone dimer (37) with hydroxide followed by neutralization afforded the uncyclized diindenone (38). en
dc.language.iso en en
dc.publisher ResearchSpace@Auckland en
dc.relation.ispartof PhD Thesis - University of Auckland en
dc.relation.isreferencedby UoA9921934914002091 en
dc.rights Restricted Item. Available to authenticated members of The University of Auckland. en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Studies in synthesis and stereochemistry en
dc.type Thesis en
thesis.degree.discipline Chemistry en
thesis.degree.grantor The University of Auckland en
thesis.degree.level Doctoral en
thesis.degree.name PhD en
dc.rights.holder Copyright: The author en


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