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II. A tandem dealkoxycarbonylation-Michael addition route to five- and six-membered lactams and lactones;
III. The synthesis of 13C-labeled d-aminolevulinic acids

dc.contributor.advisorBunce, Richard A.
dc.contributor.authorSchilling, Curtis L., III
dc.date.accessioned2016-04-25T21:16:37Z
dc.date.available2016-04-25T21:16:37Z
dc.date.issued1996-12
dc.identifier.urihttps://hdl.handle.net/11244/34024
dc.formatapplication/pdf
dc.languageen_US
dc.rightsCopyright is held by the author who has granted the Oklahoma State University Library the non-exclusive right to share this material in its institutional repository. Contact Digital Library Services at lib-dls@okstate.edu or 405-744-9161 for the permission policy on the use, reproduction or distribution of this material.
dc.titleI. Tandem dealkoxycarbonylation Michael addition route to highly functionalized cyclohexaneacetic esters
dc.titleII. A tandem dealkoxycarbonylation-Michael addition route to five- and six-membered lactams and lactones
dc.titleIII. The synthesis of 13C-labeled d-aminolevulinic acids
dc.contributor.committeeMemberEssenberg, Richard
dc.contributor.committeeMemberFord, Warren T.
dc.contributor.committeeMemberHolt, Elizabeth M.
dc.contributor.committeeMemberMottola, Horatio A.
osu.filenameThesis-1996D-S334t.pdf
osu.accesstypeOpen Access
dc.type.genreDissertation
dc.type.materialText
thesis.degree.disciplineChemistry
thesis.degree.grantorOklahoma State University


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