Total Synthesis and Stereochemical Revision of Ciliatamides A-C, Total Synthesis of 8-epi-Lucentamycin A, and Development of Microwave Methodology to Facilitate the Synthesis of BMP Inhibitors

dc.contributor.committeeChairCraig W. Lindsley
dc.contributor.committeeMemberBrian O. Bachmann
dc.contributor.committeeMemberCharles C. Hong
dc.contributor.committeeMemberGary A. Sulikowski
dc.creatorDaniels, Richard Nathan
dc.date.accessioned2020-08-22T21:08:02Z
dc.date.available2010-09-28
dc.date.issued2010-09-28
dc.description.abstractThis dissertation describes advances in total synthesis, synthetic methodology, and chemical biology. The total synthesis and stereochemical revision of Ciliatamides A-C will be discussed in detail. Also, the total synthesis of 8-epi-Lucentamycin A will be described. Lastly discussed is the development of microwave methodology to improve the synthesis of pyrazolo[1,5-a]pyrimidines. This new methodology was used to rapidly optimize a lead pyrazolo[1,5-a]pyrimidine screening hit into a highly selective and potent bone morphogenetic protein (BMP) inhibitor as well as selective KDR inhibitors using zebrafish as an in vivo screening tool.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-09272010-171411
dc.identifier.urihttp://hdl.handle.net/1803/14242
dc.subjectBone Morphogenetic Protein
dc.subjectTotal Synthesis
dc.subjectMicrowave Methodolgy
dc.subjectMedicinal Chemistry
dc.titleTotal Synthesis and Stereochemical Revision of Ciliatamides A-C, Total Synthesis of 8-epi-Lucentamycin A, and Development of Microwave Methodology to Facilitate the Synthesis of BMP Inhibitors
dc.typedissertation
dc.type.materialtext
local.embargo.lift2010-09-28
local.embargo.terms2010-09-28
thesis.degree.disciplineChemistry
thesis.degree.grantorVanderbilt University
thesis.degree.leveldissertation
thesis.degree.namePHD

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