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dc.contributor.advisor Fukuyama, Tohru
dc.creatorLi, Tangqing
dc.date.accessioned 2009-06-03T23:53:52Z
dc.date.available 2009-06-03T23:53:52Z
dc.date.issued 1994
dc.identifier.urihttps://hdl.handle.net/1911/16751
dc.description.abstract Two 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.extent 168 p.
dc.format.mimetype application/pdf
dc.language.iso eng
dc.subjectOrganic chemistry
Biochemistry
dc.title Synthetic studies towards the total synthesis of discorhabdin C
dc.type.genre Thesis
dc.type.material Text
thesis.degree.department Chemistry
thesis.degree.discipline Natural Sciences
thesis.degree.grantor Rice University
thesis.degree.level Doctoral
thesis.degree.name Doctor of Philosophy
dc.identifier.citation Li, Tangqing. "Synthetic studies towards the total synthesis of discorhabdin C." (1994) Diss., Rice University. https://hdl.handle.net/1911/16751.


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