Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 洪豪志 | en_US |
dc.contributor.author | 吳獻仁 | en_US |
dc.contributor.author | Hsien-Jen Wu | en_US |
dc.date.accessioned | 2014-12-12T02:31:25Z | - |
dc.date.available | 2014-12-12T02:31:25Z | - |
dc.date.issued | 2002 | en_US |
dc.identifier.uri | http://140.113.39.130/cdrfb3/record/nctu/#NT910500019 | en_US |
dc.identifier.uri | http://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.abstract | We 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.iso | zh_TW | en_US |
dc.subject | 4+2 環化反應 | zh_TW |
dc.subject | 碘誘導環化反應 | zh_TW |
dc.subject | Diels-Alder reaction | en_US |
dc.subject | Iodine-Induced Cyclization | en_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.title | Iodine-Induced Cyclization of the Adducts of Dihydropyranones with Cyclopentadiene | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | 應用化學系碩博士班 | zh_TW |
Appears in Collections: | Thesis |