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Total synthesis of (-)-tetrazomine and biochemical studies

dc.contributor.authorScott, Jack David, author
dc.contributor.authorWilliams, Robert M., advisor
dc.date.accessioned2022-11-28T17:46:49Z
dc.date.available2022-11-28T17:46:49Z
dc.date.issued2001
dc.description.abstractThe total synthesis of (-)-tetrazomine is presented in which the relative and absolute stereochemistry of the natural product has been determined. The synthesis features a unique iminium cyclization followed by a 1,3-dipolar cylcoaddition. The stereochemistry of advance intermediates were determined by extensive 2D NMR techniques. The asymmetric synthesis of all four stereoisomers of β-hydroxy pipecolic acid has also been described. These stereoisomers were compared to the amino acid isolated from the hydrolysis of tetrazomine to determine the absolute stereochemistry of the amino acid moiety on the natural product. The route used to complete the total synthesis allowed for pipecolic acid analogs to be synthesized in order to study the effect of structure on the biochemical characteristics of these compounds. Along with oxazolidine ring containing analogs, ring opened amino nitrile analogs were also studied.
dc.format.mediumdoctoral dissertations
dc.identifier.urihttps://hdl.handle.net/10217/235860
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relationCatalog record number (MMS ID): 991013161609703361
dc.relationQP552.T45S25 2001
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subject.lcshTetrazomine
dc.titleTotal synthesis of (-)-tetrazomine and biochemical studies
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineChemistry
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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