| 研究生: |
蔡啟輝 Tsai, Chi-Huai |
|---|---|
| 論文名稱: |
2-苯甲醯-1,4-苯醌化合物與β-雙酮基化合物的離子性反應 Ionic Reactions of 2-Benzoyl-1,4-Benzoquinones with β-Diketone Compounds |
| 指導教授: |
莊治平
Chuang, Che-Ping |
| 學位類別: |
碩士 Master |
| 系所名稱: |
理學院 - 化學系 Department of Chemistry |
| 論文出版年: | 2008 |
| 畢業學年度: | 96 |
| 語文別: | 中文 |
| 論文頁數: | 75 |
| 中文關鍵詞: | 醛醇縮合反應 、苯酚 、苯醌 |
| 外文關鍵詞: | Robinson annulation, aldol condensation |
| 相關次數: | 點閱:85 下載:2 |
| 分享至: |
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在有機合成中,碳-碳鍵的生成扮演了重要的角色,一般而言,親核性加成反應為較常使用的合成策略,本篇論文主要探討具親電性的醌類化合物和具親核性的β-雙酮基化合物所進行的加成反應,並進一步衍生合成出各種天然物的骨架。本篇論文主要分為兩個部分討論:
(1)2-苯甲醯-1,4-苯醌化合物與β-雙酮基化合物的反應
(2)2-苯甲醯苯酚化合物的合成應用
Nucleophilic addition reaction is one of the major methods to form carbon-carbon bond in organic synthesis. Taking advantage of electrophilic quinones and nucleophilic β-dicarbonyl compounds to generate addition compounds, which can be further functionalized, giving access to several skeletons of natural products. Surprisingly, an unexpected compound was found via acetyl group rearrangement. The content is separated into two parts:
(1)Reactions of 2-benzoyl-1,4-benzoquinones and β-diketone compounds.
(2)Synthetic applications of 2-benzoylphenols.
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