Model studies for the total synthesis of oscillatoxin A

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dc.creatorCunningham, Raymond Thomas
dc.date.accessioned2016-11-14T23:08:40Z
dc.date.available2011-02-18T23:08:30Z
dc.date.available2016-11-14T23:08:40Z
dc.date.issued1988-12
dc.degree.departmentChemistryen_US
dc.description.abstractThis account will describe the results of research on a model study for the total synthesis of oscillatoxin A. During the course of this work, major subunits of the target molecule were assembled and protecting group schemes were devised for use during the total synthesis. In addition, a new method for the selective benzylation of 1,2-diols was developed, and a new and highly efficient method for the synthesis of 3-deoxy-L-pentoses, compounds which are useful for the synthesis of nucleoside analogues, was discovered.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/2346/19480en_US
dc.language.isoeng
dc.publisherTexas Tech Universityen_US
dc.rights.availabilityUnrestricted.
dc.subjectMarine toxinsen_US
dc.subjectNatural productsen_US
dc.titleModel studies for the total synthesis of oscillatoxin A
dc.typeDissertation

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