Base catalyzed elimination of methyl enol ethers

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dc.contributor.advisorWenkert, Ernesten_US
dc.creatorMoreno, Louis Norman (b. 1952)en_US
dc.date.accessioned2018-12-18T21:23:49Zen_US
dc.date.available2018-12-18T21:23:49Zen_US
dc.date.issued1977en_US
dc.description.abstractThe formation of naphthalenes on treatment of enol ethers of tetralones with strong bases proceeded in good yields under moderate conditions. Dienol ethers of octalinones gave tetralins in lower yields and under more vigorous conditions. Monocyclic dienol di-ethers gave aryl ethers, while monocyclic enol ethers failed to give dienes. Attempts to generate trienes from bicyclic, non-aromatizable dienol ethers failed and resulted in isomerization of the double bonds.en_US
dc.format.digitalOriginreformatted digitalen_US
dc.format.extent71 ppen_US
dc.identifier.callnoThesis Chem. 1977 Morenoen_US
dc.identifier.citationMoreno, Louis Norman (b. 1952). "Base catalyzed elimination of methyl enol ethers." (1977) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/104478">https://hdl.handle.net/1911/104478</a>.en_US
dc.identifier.digitalRICE2113en_US
dc.identifier.urihttps://hdl.handle.net/1911/104478en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.titleBase catalyzed elimination of methyl enol ethersen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentChemistryen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Artsen_US
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