Cyclopropanation of dienol ethers

dc.contributor.advisorWenkert, Ernest
dc.creatorRanu, Brindaban Chandra
dc.date.accessioned2018-12-18T21:23:50Z
dc.date.available2018-12-18T21:23:50Z
dc.date.issued1977
dc.descriptionText includes handwritten formulas
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.
dc.format.digitalOriginreformatted digital
dc.format.extent73 pp
dc.identifier.callnoThesis Chem. 1977 Ranu
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>.
dc.identifier.digitalRICE2114
dc.identifier.urihttps://hdl.handle.net/1911/104479
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.titleCyclopropanation of dienol 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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