| 研究生: |
黃敬淳 Huang, Jing-Chun |
|---|---|
| 論文名稱: |
吲哚化合物的氧化性自由基反應 Oxidative Free Radical Reaction of Indoles |
| 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: | 2006 |
| 畢業學年度: | 94 |
| 語文別: | 中文 |
| 論文頁數: | 93 |
| 中文關鍵詞: | 醋酸錳 、氧化性自由基 、吲哚化合物 |
| 外文關鍵詞: | indole, oxidative free-radical, manganese(III) acetate |
| 相關次數: | 點閱:85 下載:1 |
| 分享至: |
| 查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報 |
近三十年來,自由基在有機合成上的應用,已逐漸受到化學家重視,尤其當自由基在進行環化時,所表現的位向及立體選擇性更受化學家所感興趣,而自由基反應又可分為還原性及氧化性自由基反應,醋酸錳(III)是一個常見的單電子氧化劑,是目前最常被用來進行氧化性自由基反應的試劑。
本論文報告分為兩部分:第一部分是利用丙烯碸吲哚化合物與對甲苯亞磺酸鈉鹽的自由基反應(式1)。第二部分則是碸基吲哚化合物與醋酸錳(III)的氧化性自由基環合反應(式2)。
Recently, reactions involving in the free radicals have widely been used in organic synthesis. These reactions exhibit interesting in regio- and stereo-selectivity. There are two categories in radical reactions. One is the reductive free-radical reaction and the other is the oxidative free-radical reaction.
Due to extensive one electron transfer of manganese(III) acetate, it has been mainly applied for the oxidant reagent in oxidative free radical reactions.
In this report, we described our results as:
(1) Sulfonyl p-toluenesulfinate in the sulfonyl radical mediated cyclizatio reaction of allysulfonylindoles(eq.1).
(2) Manganese(III)-based oxidative free radical cyclization reactions of sulfonyl group substituted indoles (eq.2) .
1. Gomberg, M. J. Am. Chem. Soc. 1900, 22, 757.
2. Hart, D. J. Science (Washington, D. C.), 1984, 223, 883.
3. Giese, B. “Radicals in Organic Synthesis: Formation of Carbon-Carbon
Bonds” Pergamon Press, Oxford, 1986.
4. Beckwith, A. L. J. Chem. Soc. Rev. 1993, 143.
5. Iqbal, J.; Bhatia, B.; Nayyar, N. K. Chem. Rev. 1994, 94, 519.
6. Curran, D. P. Synthesis 1988, 417 and 489.
7. Philippe, R,; Mukund, P. S. “Radicals in Organic Synthesis”, Wiley-VCH,
N.Y., 2001.
8. Curran, D. P.; Rakiewicz, D.M. J. Am. Chem. Soc. 1985, 107, 1448.
9. Ladlow, M.; Pattenden, G. J. Chem. Soc., Perkin Trans. 2 1988, 1107.
10.Lee, E.; Lim, J. W.; Yoon, C. H.; Sung, Y.-S.; Kim, Y. K.; J. Am. Chem.
Soc. 1997, 119, 8391.
11.Hamelin, O., Deprés, J,-P.; Greene, A. E.; J. Am. Chem. Soc. 1996, 118,
9992.
12.(a)Corey, E. J.; Kang, M. C. J. Am. Chem. Soc. 1985, 106, 5384.
(b)Snider, B. B.; Mohan, R.; Kates, S.A. J. Org. Chem. 1985, 50, 3659.
(c)Snider, B. B.; Wan, B. Y.-F; Buckman, B. O.; Foaman, B. M. J. Org. Chem.
1991, 56, 328.
(d)Snider, B. B.; Merrit, J. E.; Sasson, M.; Kates, S. A. Tetrahedron Lett.
1988, 29, 5209.
13.(a)Chuang, C.-P. Tetrahedron Lett. 1992, 33, 6311.
(b)Chuang, C.-P.; Wang, S.-F. Synth. Commun. 1995, 25, 3549.
(c)Bertrand, M. P. Org. Prep. and Proc. Int. 1994, 26, 257.
14.de Silva Correa, C. C. M.; Fleming, M. D. C. M. J. Chem. Soc., Perkin
Trans. 2 1987, 103.
15.Bristow, G. M.; Dainton, F. S. J. Proc. Roy. Soc. London, 1955, 509.
16.Accher, M.; Vofsi, D. J. Chem. Soc. 1964, 4962.
17.Wang, S.-F.; Chuang, C.-P.; Lee, J,-H.; Liu, S,-T. Tetrahedron 1999, 55,
2273.
18.Chuang, C.-P.; Wang, S.-F. Synlett. 1995, 763.
19.Zard, S. Z.; Quiclet-Sire, B. J. Am. Chem. Soc. 1997, 119, 7410.
20.Wang, S.-F.; Chuang, C.-P.; Lee, W.-H. Tetrahedron 1999, 55, 6109.
21.Sinder, B. B. Chem. Rev. 1996, 96, 339.
22.Mohan, R. P.; Kates, S. A.; Dombroski, M.; Sinder, B. B. Tetrahedron
Lett. 1987, 28, 814.
23.Sinder, B. B.; Zhang. Q.; Domvbroski, M. A. J. Org. Chem. 1992, 57, 4195.
24.Sinder, B. B.; Zhang. Q. J. Org. Chem. 1993, 58, 3185.