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oai:www.ideals.illinois.edu:2142/84208 2023-07-11 col_2142_5131 col_2142_14789 com_2142_5130 com_2142_14788 com_2142_8903

Coates, Robert M. Zhao, Yuxin 2015-09-25T22:13:29Z 2015-09-25T22:13:29Z 10000-01-01 2005 2005 The final part of this thesis discusses the preparation and characterization of two deoxycapsidiols as well as a series of capsidiol analogs including epiaristolochene and two isomers. Overall, ten capsidiol derivatives were synthesized from capsidiol and sent to collaborators for various biological evaluations. In addition, this library was evaluated for antifungal activity in order to establish preliminary structure-activity relationships. Made available in DSpace on 2015-09-25T22:13:29Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 3199199.pdf: 4442856 bytes, checksum: 2ad3b0a112359615f5b873509ddf24fe (MD5) Previous issue date: 2005 Embargo set by: Seth Robbins for item 85489 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs U of I Only 186 p. Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2005. http://hdl.handle.net/2142/84208 (MiAaPQ)AAI3199199 eng Chemistry, Organic Modified Farnesyl Diphosphate, Germacrane, and Eremophilane Sesquiterpenes as Probes for Capsidiol *Biosynthesis text Chemistry Chemistry University of Illinois at Urbana-Champaign Dissertation Ph.D.