完整後設資料紀錄
DC 欄位語言
dc.contributor.author龔亮仁en_US
dc.contributor.authorLiang-Rern Kungen_US
dc.contributor.author何子樂en_US
dc.contributor.authorDr. Tse-Lok Hoen_US
dc.date.accessioned2014-12-12T02:21:33Z-
dc.date.available2014-12-12T02:21:33Z-
dc.date.issued1998en_US
dc.identifier.urihttp://140.113.39.130/cdrfb3/record/nctu/#NT870500035en_US
dc.identifier.urihttp://hdl.handle.net/11536/64814-
dc.description.abstractzh_TW
dc.description.abstract(I) The total synthesis of 2-isocyanoallopupukeanane, a metabolite secreted by nudibranch mollusks, was accomplished in nineteen steps from cyclopentadiene in ca. 5% overall yield. A highly stereoselective synthesis of this unique compound by sigmatropic reaction is the subject of our synthetic strategy. (II) Kainic acid, one of the representative agonists of excitatory amino acid receptors, has attracted considerable interest due to its unique structure and neuroexcitatory properties. While the total synthesis of this trisubstituted pyrrolidine ring have already been reported by several research groups, our approach to the kainic acid relied on the Diels-Alder reaction of N-butadienyl amide with methyl acrylate.en_US
dc.language.isoen_USen_US
dc.subjectzh_TW
dc.subject2-Isocyanoallopupukeananeen_US
dc.subjectKainic aciden_US
dc.title海產天然物合成研究zh_TW
dc.titleSynthetic study of marine natural productsen_US
dc.typeThesisen_US
dc.contributor.department應用化學系碩博士班zh_TW
顯示於類別:畢業論文