Synthetic studies on naphthyridinomycin: A total synthesis of (+)-cyanocycline A

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dc.contributor.advisorFukuyama, Tohru
dc.creatorLi, Leping
dc.date.accessioned2009-06-04T08:48:38Z
dc.date.available2009-06-04T08:48:38Z
dc.date.issued1989
dc.description.abstractA synthetic route via chiral precursor 74* had led to a total synthesis of (+)-cyanocycline A. This optically pure synthesis unequivocally determined the absolute stereochemistry of natural cyanocycline A as 2, in contrast to a previously reported X-ray crystallographic assignment as presented on 2$\prime$. ftn*Please refer to dissertation for diagrams.
dc.format.extent161 p.en_US
dc.format.mimetypeapplication/pdf
dc.identifier.callnoThesis Chem. 1989 Li
dc.identifier.citationLi, Leping. "Synthetic studies on naphthyridinomycin: A total synthesis of (+)-cyanocycline A." (1989) Diss., Rice University. <a href="https://hdl.handle.net/1911/19066">https://hdl.handle.net/1911/19066</a>.
dc.identifier.urihttps://hdl.handle.net/1911/19066
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 on naphthyridinomycin: A total synthesis of (+)-cyanocycline A
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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