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dc.contributor.advisorBates, Robert B.en_US
dc.contributor.authorCamou-Arriola, Fernando Alberto Josue.
dc.creatorCamou-Arriola, Fernando Alberto Josue.en_US
dc.date.accessioned2011-10-31T17:18:01Z
dc.date.available2011-10-31T17:18:01Z
dc.date.issued1989en_US
dc.identifier.urihttp://hdl.handle.net/10150/184773
dc.description.abstractStructures were determined for 48 new natural products and several related compounds by NMR methods. One new natural product and two unnatural product structures were determined by X-ray diffraction. Molecular mechanics calculations on two indoles related to the neurotransmitter serotonin and on some synthetic cyclophanes were used to gain information about their preferred conformations. Considerable time is wasted redetermining the structures of known natural products when they are encountered in new sources. To help alleviate this problem, a database which searches on proton NMR chemical shifts was developed.
dc.language.isoenen_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.subjectChemical structure.en_US
dc.subjectNuclear spectroscopy.en_US
dc.subjectX-rays -- Diffraction.en_US
dc.subjectNatural products -- Spectra -- Databases.en_US
dc.titleStructure determinations of natural products and related molecules.en_US
dc.typetexten_US
dc.typeDissertation-Reproduction (electronic)en_US
dc.identifier.oclc702683610en_US
thesis.degree.grantorUniversity of Arizonaen_US
thesis.degree.leveldoctoralen_US
dc.identifier.proquest9000767en_US
thesis.degree.disciplineChemistryen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.namePh.D.en_US
refterms.dateFOA2018-06-16T23:43:11Z
html.description.abstractStructures were determined for 48 new natural products and several related compounds by NMR methods. One new natural product and two unnatural product structures were determined by X-ray diffraction. Molecular mechanics calculations on two indoles related to the neurotransmitter serotonin and on some synthetic cyclophanes were used to gain information about their preferred conformations. Considerable time is wasted redetermining the structures of known natural products when they are encountered in new sources. To help alleviate this problem, a database which searches on proton NMR chemical shifts was developed.


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