| 研究生: |
陳政良 Chen, Cheng-Liang |
|---|---|
| 論文名稱: |
硫代苯甲醯胺苯化合物之氧化性自由基環合反應 Oxidative Free Radical Cyclization Reaction of Thiobenzanilides |
| 指導教授: |
莊治平
Chuang, Chih-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: | 2011 |
| 畢業學年度: | 99 |
| 語文別: | 中文 |
| 論文頁數: | 107 |
| 中文關鍵詞: | 自由基反應 、錳 、硫代苯甲醯胺苯化合物 |
| 外文關鍵詞: | radical reaction, Mn, Thiobenzanilide |
| 相關次數: | 點閱:51 下載:1 |
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近三十年來,在有機合成的領域裡,利用自由基反應來生成碳-碳鍵的方法已受到相當的注目,尤其當自由基在環化時所表現的位向及立體選擇性更受化學家所感興趣。其中在氧化性自由基反應中,醋酸錳(III)和硝酸銀(I)常被當作自由基反應的試劑。
本篇論文可分為三部分:
第一,主要是利用醋酸錳(III)為自由基的起始劑,來探討硫代苯甲醯胺苯化合物之氧化性自由基環合反應。第二,研究硫代苯甲醯胺萘化合物之氧化性自由基環合反應。第三,關於2-鹵基苯甲醯胺苯化合物的硫化環合反應。
Free radical reaction has received considerable attention in organic synthesis for the formation of carbon-carbon bonds in the last three decades. Especially, these reactions exhibit interesting in regio- and stereo-selectivity. Among these, manganese(III) acetate and silver(I) nitrate have been used as reagents in oxidative free radical reactions.
There are three parts in this thesis:
(1) With oxidative free radical cyclization reaction of thiobenzanilides by using of manganese (III) acetate as free radical initiator.
(2) Oxidative free radical cyclization reaction of naphthylbenzamides.
(3) Thionation and cyclization of 2-halobenzanilides.
1. Philippe, R.; Mukund, P. S. Radicals in Organic Synthesis Volume 1:
Basic Principles: WILEY-VCH, 2001, 1-10.
2. Snider, B. B. Chem. Rev. 1996, 96, 339-363.
3. Malcolm, F. G.; Carol, J. M.; Peter, L.; Peter, A.; Audrey, R.; Donna,
E. J. Med. Chem. 1994, 37, 1689-1695.
4. Downer-Riley, N. k.; Jackson, Y. A.; Tetrahedron 2008, 64, 7741-
7744.
5. Mu, X.-J.; Zou, J.-P.; Zeng, R.-S.; Wu, J.-C. Tetrahedron Lett. 2005, 46,
4345-4347.
6. Snider, B. B.; Mohan, R.; Kates, S. A. J. Org. Chem. 1985, 50,
3661-3663.
7. Snider, B. B.; Mohan, R.; Kates, S. A. Tetrahedron Lett. 1987, 28,
841-844.
8. Mohan, R.; Kates, S. A.; Dombroski, M. A.; Snider, B. B. Tetrahedron
Lett. 1987, 28, 845-848.
9. Snider, B. B.; Patricia, J. J.; Kates, S. A. J. Org. Chem. 1988, 53,
2137-2143.
10. Snider, B. B.; Patricia, J. J. J. Org. Chem. 1989, 54, 38-46.
11. Snider, B. B.; Buckman, B. O. Tetrahedron 1989, 45, 6969-6978.
12. Kates, S. A.; Dombroski, M. A.; Snider, B. B. J. Org. Chem. 1990, 55,
2427-2436.
13. Dombroski, M. A.; Kates, S. A.; Snider, B. B. J. Am. Chem. Soc. 1990,
112, 2759-2767.
14. Snider, B. B.; Wan, B. Y. F.; Buckman, B. O.; Foxman, B. M. J. Org.
Chem. 1991, 56, 328-334.
15. Dombroski, M. A.; Snider, B. B. Tetrahedron 1992, 48, 1417-1426.
16. Snider, B. B.; McCarthy, B. A. J. Org. Chem. 1993, 58, 6217-3663.
17. Snider, B. B.; Kiselgof, J. Y.; Foxman, B. M. J. Org. Chem. 1998, 63,
7945-7952.
18. Snider, B. B.; Duvall, J. R. Org. Lett. 2004, 6, 1265-1268.
19. Ishibashi, H.; Toyao, A.; Takeda, Y. Synlett 1999, 1468-1470.
20. Tsai, A.-I.; Wu, Y.-L.; Chuang, C.-P. Tetrahedron 2001, 57, 7829-7837.
21. Wang, G.-W.; Dong Y.-W.; Wu P.; Yuan T.-T.; Shen, Y.-B. J. Org.
Chem. 2008, 73, 7088-7095.
22. Hu, W.-P.; Chen, Y.-K.; Liao, C.-C.; Yu, H.-S.; Tsai, Y.-M.; Huang,
S.-M.; Tsai, F.-Y.; Shen, H.-C.; Chang, L.-S.; Wang, J.-J. Bioorg. Med. Chem. 2010, 18, 6197–6207.
23. Shi, D.-F.; Bradshaw, T. D.; Wrigley, S.; McCall, C. J.; Lelieveld, P.;
Fichtner, I.; Stevens, M. F. G. J. Med. Chem. 1996, 39, 3375- 3384.
24. Loaiza-Pe´rez, A. L.; Trapani, V.; Hose, C.; Singh, S. S.; Trepel, J.; Stevens, M. F. G.; Bradshaw, T. D.; Sausville, E. A. Mol. Pharmacol. 2002, 61, 13-19.
25. Trapani, V.; Patel, V.; Ciolino, H. P.; Yeh, G. C.; Hose, C.; Trepel, J. B.; Stevens, M. F. G.; Sausville, E. A.; Loaiza-Pe´rez, A. L. Br. J. Cancer 2003, 88, 599-605.
26. Hutchinson, I.; Chua, M. S.; Browne, H. L.; Trapani, V.; Bradshaw, T. D.; Westwell, A. D.; Stevens, M. F. G. J. Med. Chem. 2001, 44, 1446–1455.
27. Bergman, J. M.; Coleman, P. J.; Cox, C.; HartmanLindsley, G. D. C.; Mercer, S. P.; Roecker, A. J.; Whitman, D. B. PCT Int. Appl. 2006, WO 2006127550.
28. Ali, A.; Taylor, G. E.; Graham, D. W. PCT Int. Appl. 2001, WO
2001028561.
29. Walling, C.; Camaioni, D. M. J. Org. Chem. 1978, 43, 3266-3271.