Synthetic studies towards the total synthesis of discorhabdin C

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dc.contributor.advisorFukuyama, Tohru
dc.creatorLi, Tangqing
dc.date.accessioned2009-06-03T23:53:52Z
dc.date.available2009-06-03T23:53:52Z
dc.date.issued1994
dc.description.abstractTwo synthetic approaches towards the total synthesis of discorhabdin C (3) are described. The general strategy for construction of azacarbocyclic spiro dienone system is to employ an intramolecular para-phenolic alkylation (58 to 43). The key reaction for the first approach is a newly improved aromatic Claisen rearrangement. The key reaction for the second approach is a novel tin-mediated indole synthesis developed in our laboratory.(DIAGRAM, TABLE OR GRAPHIC OMITTED...PLEASE SEE DAI)
dc.format.extent168 p.en_US
dc.format.mimetypeapplication/pdf
dc.identifier.callnoTHESIS CHEM. 1994 LI
dc.identifier.citationLi, Tangqing. "Synthetic studies towards the total synthesis of discorhabdin C." (1994) Diss., Rice University. <a href="https://hdl.handle.net/1911/16751">https://hdl.handle.net/1911/16751</a>.
dc.identifier.urihttps://hdl.handle.net/1911/16751
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.subjectOrganic chemistry
dc.subjectBiochemistry
dc.titleSynthetic studies towards the total synthesis of discorhabdin C
dc.typeThesis
dc.type.materialText
thesis.degree.departmentChemistry
thesis.degree.disciplineNatural Sciences
thesis.degree.grantorRice University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy
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