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dc.contributor.author洪豪志en_US
dc.contributor.author吳獻仁en_US
dc.contributor.authorHsien-Jen Wuen_US
dc.date.accessioned2014-12-12T02:31:25Z-
dc.date.available2014-12-12T02:31:25Z-
dc.date.issued2002en_US
dc.identifier.urihttp://140.113.39.130/cdrfb3/record/nctu/#NT910500019en_US
dc.identifier.urihttp://hdl.handle.net/11536/70896-
dc.description.abstract進一步系統性地探討二氫吡喃酮衍生物與環戊二烯Diels-Alder反應之加成物7-9,其碘誘導環化反應之位向選擇性,並利用NOE光譜定出其立體結構。 化合物7-9進行碘誘導環化反應具有很好的位向選擇性,更進一步探討其類似物:化合物25、26(多延伸出一個碳)之碘誘導環化反應。 同時探討二氫吡喃酮衍生物與環戊二烯在路易士酸催化下之Diels-Alder反應。zh_TW
dc.description.abstractWe systemically further discuss Diels-Alder reaction adducts (7-9) from pyranone derivatives and cyclopentadiene undergo iodolactonization , the stereoselective in this reaction is very high . Because the stereoselective is very high in the reaction which adducts (7-9) undergo iodolactonization , further we want to discuss compound (7-9) derivatives, as compound (25、26), which stereoselective is high or not in iodolactonization . Discuss the Diels-Alder reaction when Lewis acid present .en_US
dc.language.isozh_TWen_US
dc.subject4+2 環化反應zh_TW
dc.subject碘誘導環化反應zh_TW
dc.subjectDiels-Alder reactionen_US
dc.subjectIodine-Induced Cyclizationen_US
dc.title二氫吡喃酮-環戊二烯加成物之碘誘導環化反應zh_TW
dc.titleIodine-Induced Cyclization of the Adducts of Dihydropyranones with Cyclopentadieneen_US
dc.typeThesisen_US
dc.contributor.department應用化學系碩博士班zh_TW
Appears in Collections:Thesis