Base catalyzed elimination of methyl enol ethers

dc.contributor.advisorWenkert, Ernest
dc.creatorMoreno, Louis Norman (b. 1952)
dc.date.accessioned2018-12-18T21:23:49Z
dc.date.available2018-12-18T21:23:49Z
dc.date.issued1977
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.
dc.format.digitalOriginreformatted digital
dc.format.extent71 pp
dc.identifier.callnoThesis Chem. 1977 Moreno
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>.
dc.identifier.digitalRICE2113
dc.identifier.urihttps://hdl.handle.net/1911/104478
dc.language.isoeng
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.
dc.titleBase catalyzed elimination of methyl enol ethers
dc.typeThesis
dc.type.materialText
thesis.degree.departmentChemistry
thesis.degree.disciplineNatural Sciences
thesis.degree.grantorRice University
thesis.degree.levelMasters
thesis.degree.nameMaster of Arts
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