Atropisomerism and the synthesis of lignans

dc.contributor.authorYau, Chien_US
dc.date.accessioned2007-07-12T17:47:49Z
dc.date.available2007-07-12T17:47:49Z
dc.date.issued2001-08-01T00:00:00Zen_US
dc.degree.disciplinePlant Scienceen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractA new synthetic methodology was developed to synthesize two chosen lignans, galbulin and cagayanin, with the intent of applying this synthetic scheme for the synthesis of structurally similar lignans. The Stobbe condensation was ideally suited for generating the starting materials for constructing the aryltetralin skeleton. Two successive Stobbe condensations were executed to generate the starting dibenzylidenesuccinates. It was discovered that triflic acid-catalyzed cyclization of these ibenzylidenesuccinates produced the desired aryltetralin lignan structures in good yields. From these aryltetralin skeletons, functional interconversions were performed ultimately to generate the two target natural lignans, galbulin and cagayanin. The dibenzylidenesuccinates, upon treatment with acid, demonstrated some intriguing chemistry. In an attempt to further understand this cyclization step, several other dibenzylidenesuccinates with different substituent patterns were synthesized. These reactions were studied in detail to investigate the effect of the substituent patterns on the outcome of the reaction. Two plausible explanations and detailed mechanisms were postulated to account for the formation of the aryltetralins with literature evidence to support these theories. Methods for coercing the dibenzylidenesuccinate to adopt one atropisomer over the other were studied and the preliminary results are presented. (Abstract shortened by UMI.)en_US
dc.format.extent6225048 bytes
dc.format.extent184 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.identifier.urihttp://hdl.handle.net/1993/2522
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.titleAtropisomerism and the synthesis of lignansen_US
dc.typemaster thesisen_US
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