二氫吡喃酮-環戊二烯加成物之碘誘導環化反應

完整後設資料紀錄

DC 欄位	值	語言
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
顯示於類別：	畢業論文