研究生: |
張加欣 Chia-Hsin Chang |
---|---|
論文名稱: |
以 Wittig-Knoevenagel 環化反應選擇性合成抗 B 型肝炎病毒藥物與其結構活性關係探討及以Friedlander 縮合反應合成含氮雜環多稠苯化合物初探 Selective Synthesis of Helioxanthin Derivatives with Anti-Hepatitis B Activities via Wittig-Knoevenagel Cyclization and Their Structure-Activity Relationship; Preliminary Studies on the Synthesis of Nitrogen Containing Acene Derivatives via Friedlander Condensation Reaction |
指導教授: |
何郡軒
Jinn-Hsuan Ho 林質修 Chih-Hsiu Lin |
口試委員: |
葉小帆
Sheau-Farn Yeh 葉名倉 Ming-Chang Yeh |
學位類別: |
碩士 Master |
系所名稱: |
應用科技學院 - 應用科技研究所 Graduate Institute of Applied Science and Technology |
論文出版年: | 2011 |
畢業學年度: | 99 |
語文別: | 中文 |
論文頁數: | 397 |
中文關鍵詞: | 木酚素 、抗B型肝炎病毒藥物 、含氮雜環多稠苯 |
外文關鍵詞: | Helioxanthin Derivatives, Anti-hepatitis B activities, Nitrogen containing acene |
相關次數: | 點閱:179 下載:1 |
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第一部分
從台灣杉單離出的木酚素 helioxanthin( HE-145 )有抑制 B 型肝炎病毒的作用。在 HE-145 結構與活性的研究中,以具內醯胺結構的HE-145 衍生物 ( HE-145-109 )抑制 B 型肝炎病毒的活性最高。論文第一部分以合成 HE-145-109 衍生物為目標,並藉由選擇性合成策略提高內醯胺衍生物的產率。在得到 20 個官能基修飾內醯胺衍生物後,經測試篩選出 6 個具抗病毒活性的衍生物。並進一步討論活性與結構間之關係。
第二部份
氮雜環多稠苯化合物較多稠苯化合物電子親和力高,一般認為其穩定性較好且有潛力成為新型負型材料。論文第二部份的目標是以 Fridlander 縮合反應將氮原子引入多稠苯的共軛系統中,以期得到吡啶結構的氮雜環五稠苯衍生物,並且藉由增加腈基的取代調控前列軌域的能階。
Part One
In previous studies, lignan helioxanthin (He-145) isolated from Taiwania cryptomerioides exhibits remarkable anti-HBV activity. During structure-activity mapping, it was discovered that one He-145 derivative with lactam structure exhibits the highest antiviral activity. In the first part of this dissertation, we developed a selective synthetic scheme for this class of compounds. In twenty compounds we synthesized, six exhibit significant anti-HBV activities. Their structure-activity relationship was also discussed.
Part Two
Nitrogen containing heteroacenes have higher electron affinity higher then their acene counterparts and therefore also more stable. It is generally recognized that this class of compounds are potential N-type materials. The second part of this dissertation focuses on using Friedlander condensation reaction to construct nitrogen containing acene conjugated systems. Several 5,12-diazapetnacene derivatives were synthesized. It is also found the frontier orbitals of these compounds can be modulated via CN substitution.
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