Cyclopropanation of dienol ethers

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dc.contributor.advisorWenkert, Ernesten_US
dc.creatorRanu, Brindaban Chandraen_US
dc.date.accessioned2018-12-18T21:23:50Zen_US
dc.date.available2018-12-18T21:23:50Zen_US
dc.date.issued1977en_US
dc.descriptionText includes handwritten formulasen_US
dc.description.abstractThe copper-catalysed, thermal decompositions of ethyl diazoacetate and diazoacetone in the presence of 1-methoxycyclohexa-1,3-diene, l-methoxy-4-methylcyclohexa-l,3-diene, 1-methoxybuta-l,3-diene, 1-ethoxybuta-l,3-diene and 1-trimethylsilyloxybuta-1,3-diene and the acid hydrolysis of the resultant cyclopropanes are described. These reactions constitute a simple, two-step procedure for the production of olefinic 1,4- and 1,6-dicarbonyl compounds, starting from dienol ethers of a,g -unsaturated aldehydes and ketones.en_US
dc.format.digitalOriginreformatted digitalen_US
dc.format.extent73 ppen_US
dc.identifier.callnoThesis Chem. 1977 Ranuen_US
dc.identifier.citationRanu, Brindaban Chandra. "Cyclopropanation of dienol ethers." (1977) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/104479">https://hdl.handle.net/1911/104479</a>.en_US
dc.identifier.digitalRICE2114en_US
dc.identifier.urihttps://hdl.handle.net/1911/104479en_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.titleCyclopropanation of dienol 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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