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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.creatorDaniels, Richard Nathan
dc.date.accessioned2020-08-22T21:08:02Z
dc.date.available2010-09-28
dc.date.issued2010-09-28
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-09272010-171411
dc.identifier.urihttp://hdl.handle.net/1803/14242
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.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.contributor.committeeMemberBrian O. Bachmann
dc.contributor.committeeMemberCharles C. Hong
dc.contributor.committeeMemberGary A. Sulikowski
dc.type.materialtext
thesis.degree.namePHD
thesis.degree.leveldissertation
thesis.degree.disciplineChemistry
thesis.degree.grantorVanderbilt University
local.embargo.terms2010-09-28
local.embargo.lift2010-09-28
dc.contributor.committeeChairCraig W. Lindsley


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