| 研究生: |
陳鉦昇 Cheng-Sheng Chen |
|---|---|
| 論文名稱: |
鈀催化含苯甲酸之烯化合物異構化反應並合成5'-epi-Aigialomycin D |
| 指導教授: |
侯敦仁
Duen-Ren Hou |
| 口試委員: | |
| 學位類別: |
碩士 Master |
| 系所名稱: |
理學院 - 化學學系 Department of Chemistry |
| 論文出版年: | 2014 |
| 畢業學年度: | 102 |
| 語文別: | 中文 |
| 論文頁數: | 217 |
| 中文關鍵詞: | 異構化 、鈀金屬催化 、環內酯 |
| 外文關鍵詞: | Aigialmycin D, isomerization, resorcyclic lactone |
| 相關次數: | 點閱:11 下載:0 |
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本篇論文發展一新方法:利用氯化鈀作為催化劑,以含苯甲酸之烯化合物作為起始物,進行烯烴異構化反應。且反應後的碳-碳雙鍵為單一E-from結構,產率達92%。應用此反應,以掌性雙烯雙醇化合物5作為起始物,合成天然物Aigialomycin D之差向異構物5'-epi-Aigialomycin D (1)。其中碳-碳鍵的生成以交叉置換反應 (Cross Metathesis) 完成,大環內酯以Yamaguchi內酯化反應建構。
A novel palladium-catalyzed isomerization of alkenylbenzoic acid has been developed. This methodology could be applied to synthesis 5'-epi-Aigialomycin D by using chiral dienediol 5 as the starting material. The key reactions included cross metathesis (CM) and Yamaguchi lactonization.
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