Synthetic studies towards the total synthesis of renieramycin A (Antibiotics)

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dc.contributor.advisorFukuyama, Tohru
dc.creatorTun, Min Min
dc.date.accessioned2009-06-04T00:14:09Z
dc.date.available2009-06-04T00:14:09Z
dc.date.issued1988
dc.description.abstractFormation of the skeleton of renieramycin A was achieved through sequential condensations of piperazinedione and substituted benzaldehydes. One of the key reactions of this synthesis, oxidation of benzylic position, produced hydroxylated compound 62 (see p. 22 in dissertation for illustration). Further elaboration of 62 has resulted in N-methyl 65 (p. 22), an important precursor to renieramycin A.
dc.format.extent137 p.en_US
dc.format.mimetypeapplication/pdf
dc.identifier.callnoThesis Chem. 1988 Tun
dc.identifier.citationTun, Min Min. "Synthetic studies towards the total synthesis of renieramycin A (Antibiotics)." (1988) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/13323">https://hdl.handle.net/1911/13323</a>.
dc.identifier.urihttps://hdl.handle.net/1911/13323
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.titleSynthetic studies towards the total synthesis of renieramycin A (Antibiotics)
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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