完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | 劉士毅 | zh_TW |
dc.contributor.author | 孫仲銘 | zh_TW |
dc.contributor.author | Liu, Shih-I | en_US |
dc.contributor.author | Sun, Chung-Ming | en_US |
dc.date.accessioned | 2018-01-24T07:38:13Z | - |
dc.date.available | 2018-01-24T07:38:13Z | - |
dc.date.issued | 2016 | en_US |
dc.identifier.uri | http://etd.lib.nctu.edu.tw/cdrfb3/record/nctu/#GT070352516 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/139654 | - |
dc.description.abstract | 利用皮克特-施彭格勒反應合成四氫異喹啉後,與異氰酸硫酯、異氰酸硒酯進行[3+2]環化反應合成咪唑並[1,5-b]異喹啉,或與氯化乙醯氯及一級胺反應合成吡嗪並[1,2-b]異喹啉,並建立分子庫。 利用金催化以一鍋化兩步的方法合成異喹啉並[1,2-a]異喹啉,第一步先進行皮克特-施彭格勒反應,第二步進行金催化6-endo-dig的環化,最後得到目標化合物異喹啉並[1,2-a]異喹啉。 | zh_TW |
dc.description.abstract | Use Pictet-Spengler reaction to synthesize tetrahydroisoquinoline then react with isocyanate, isothiocyanate, isoselenocyanate via [3 + 2] cycloaddition to obtain imidazo[1,5-b]isoquinoline, or react with chloroacetyl chloride then follow by primary amine to obtain pyraz[1,2-b]isoquinoline, and build up the molecular libraries. Gold-Assisted one-pot two-step synthesis of isoquinolino[1,2-a]isoquinoline. First step undergo Pictet-Spengler reaction, then second step follow by gold catalyze 6-endo-dig cyclization to give the isoquinolino[1,2-a]isoquinoline. | en_US |
dc.language.iso | zh_TW | en_US |
dc.subject | 四氫異喹啉 | zh_TW |
dc.subject | 皮克特-施彭格勒反應 | zh_TW |
dc.subject | 金催化 | zh_TW |
dc.subject | tetrahydroisoquinoline | en_US |
dc.subject | Pictet-Spengler reaction | en_US |
dc.subject | gold catalyze | en_US |
dc.title | 合成四氫異喹啉衍生物分子庫及利用金催化合成異喹啉並[1,2-a]異喹啉衍生物 | zh_TW |
dc.title | Synthesis of Tetrahydroisoquinoline Derivatives Molecular Library and Gold-Assisted Synthesis of Isoquinolino[1,2-a]isoquinoline Derivatives | 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 |