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dc.contributor.advisor Fukuyama, Tohru
dc.creatorLi, Leping
dc.date.accessioned 2009-06-04T08:48:38Z
dc.date.available 2009-06-04T08:48:38Z
dc.date.issued 1989
dc.identifier.urihttps://hdl.handle.net/1911/19066
dc.description.abstract A 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.extent 161 p.
dc.format.mimetype application/pdf
dc.language.iso eng
dc.subjectOrganic chemistry
dc.title Synthetic studies on naphthyridinomycin: A total synthesis of (+)-cyanocycline A
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, Leping. "Synthetic studies on naphthyridinomycin: A total synthesis of (+)-cyanocycline A." (1989) Diss., Rice University. https://hdl.handle.net/1911/19066.


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