Synthetic studies on the discorhabdins

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dc.contributor.advisorCiufolini, Marco A.en_US
dc.creatorYates, Matthew H.en_US
dc.date.accessioned2009-06-04T06:31:42Zen_US
dc.date.available2009-06-04T06:31:42Zen_US
dc.date.issued2000en_US
dc.description.abstractThe discorhabdins are a family of chemically and biologically interesting natural products. Previous syntheses of these complex substances have all been very similar; this similarity is limiting to the flexibility of these approaches. We describe a general method which we believe can diverge to make any number of the natural products. This route is based on novel benzoquinone photochemistry followed by an annulation onto a quinone monoketal to give the core structure. This core can then be advanced appropriately to form the natural products.* *Please refer to dissertation for diagrams.en_US
dc.format.extent196 p.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.callnoTHESIS CHEM. 2000 YATESen_US
dc.identifier.citationYates, Matthew H.. "Synthetic studies on the discorhabdins." (2000) Diss., Rice University. <a href="https://hdl.handle.net/1911/19572">https://hdl.handle.net/1911/19572</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/19572en_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.subjectOrganic chemistryen_US
dc.titleSynthetic studies on the discorhabdinsen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentChemistryen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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