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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 蔡蘊明(Yenu-Min Tasi) | |
dc.contributor.author | Yi-Hsuan Chang | en |
dc.contributor.author | 張怡萱 | zh_TW |
dc.date.accessioned | 2021-06-13T01:19:23Z | - |
dc.date.available | 2007-07-23 | |
dc.date.copyright | 2007-07-23 | |
dc.date.issued | 2007 | |
dc.date.submitted | 2007-07-17 | |
dc.identifier.citation | 參 考 文 獻
1. (a) Gomberg, M. Chem. Ber. 1900, 33, 3150. (b) Gomberg, M. J. Am. Chem. Soc. 1900, 22, 757. (c) Paneth, F.; Hofeditz, W. Ber. 1929, 62, 1335. (d) Waters, W. A. J. Chem. Soc. 1937, 113. (d) Donald H. Hey; William A. Waters. Chem. Rev. 1937, 21, 169. (e) McBride, J. M.; Skinner, K. J.; Hochster, H. S. J. Am. Chem. Soc. 1974, 96, 4301. 2. (a) Fossy, J.; Lefort, D.; Sorba, J. Free Radical in Organic Chemistry; Wiley: New York, 1995. (b) Motherwell, W. B.; Crich, D. Free radical Chain Reaction in Organic Synthesis; Academic Press: New York, 1992. (c) Renaud, P.; Sibi, M. P., Eds. Radical in Organic Synthesis; Wiley-VCH: Weinhein, 2001. 3. Giese, B.; Kopping, B.; Grobel, T.; Dickhaut, J.; Thoma, G.; Kulicke, K. J.; Trach, F. Org. React. 1996, 48, 303. 4. (a) Dennis P. Curran; Ned A. Porter; Bernd Giese. Stereochemistry of Radical Reactions; VCH:Weinheim, New York, 1996. (b) Giese, B. Angew. Chem. Int. Ed. Eng. 1989, 28, 969. 5. (a) Beckwith, A. L. J.; Hay, B. P. J. Am. Chem. Soc. 1989, 111, 230. (b) Beckwith, A. L. J.; Hay, B. P. J. Am. Chem. Soc. 1989, 111, 2674. (c) Beckwith, A. L. J.; Raner, K. D. J. Org. Chem. 1992, 57, 4954. 6. (a) Tsang, R.; Fraser-Reid, B. J. Am. Chem. Soc. 1986, 108, 2116. (b) Tsang, R.; Fraser-Reid, B. J. Am. Chem. Soc. 1986, 108, 8102. (c) Tsang, R.; Dickson, J. K., Jr.; Pak, H.; Walton, R.; Fraser-Reid, B. J. Am. Chem. Soc. 1987, 109, 3484. (d) Fraser-Reid, B.; Vite, G. D.; Yeung, B.-W. A.; Tsang, R. Tetrahedron Lett. 1988, 29, 1645. (e) Dickson, J. K., Jr.; Tsang, R.; Llera, J. M.; Fraser-Reid, B. J. Org. Chem. 1989, 54, 5350. (f) Walton, R.; Fraser-Reid, B. J. Am. Chem. Soc. 1991, 113, 5791. 7. (a) Jung, M. E.; Gervay, J. J. Am. Chem. Soc. 1991, 113, 224. (b) Lightstone, F. C.; Bruice, T. C. J. Am. Chem. Soc. 1994, 116, 10789. (c) Parrill, A. L.; Dolata, D. P. J. Mol. Struct. (THEOCHEM) 1996, 370, 187. (d) Kirby, A. J. Adv. Phys. Org. Chem. 1980, 17, 183. 8. (a) Dowd, P.; Choi, S. C. J. Am. Chem. Soc. 1987, 109, 3493. (b) Dowd, P.; Mahmood, K.; Collins, M. R.; Zhang, W. Tetrahedron Lett. 1995, 36, 2729 and references cited therein. 9. (a) Beckwith, A. L. J.; O’Shea, D. M.; Westwood, S. W. J. Am. Chem. Soc. 1988, 110, 2565. (b) Beckwith, A. L. J.; O’Shea, D. M.; Gerba, S.; Westwood, S. W. J. Chem. Soc., Chem. Commum. 1987, 666. 10. (a) Curran, D. P.; Liu, H. J. Org. Chem. 1991, 56, 3463. (b) Curran, D. P.; Palovich, M. Synlett 1992, 631. (c) Curran, D. P.; Diederichsen, U.; Palovich, M. J. Am. Chem. Soc. 1997, 119, 4797. 11. Kim, S.; Jon, S. Y. J. Chem. Soc., Chem. Commun. 1996, 1335. 12. Kim, S.; Oh, D. H. Synlett. 1998, 525. 13. (a) Chang, S.-Y.; Jiaang, W.-T.; Cherng, C.-D.; Tang, K.-H.; Huang, C.-H.; Tsai, Y.-M. J. Org. Chem. 1997, 62, 9089. (b) Jiaang, W.-T.; Tang, K.-H.; Chang, L.-B.; Tsai, Y.-M. J. Org. Chem. 1999, 64, 618. (c) Huang, C.-H.; Chang, S.-Y.; Wang, N.-S.; Tsai, Y.-M.; J. Org. Chem. 2001, 66, 8983. 14. (a) Dalton, J. C.; Borque, R. A. J. Am. Chem. Soc. 1981, 103, 699. (b) Harris, J. M.; MacInnes, I.; Walton, J. C.; Maillard, B. J. Organomet. Chem. 1991, 403, C25 (c) Tsai, Y.-M.; Ke, B.-W. J. Chin. Chem. Soc. (Taipei) 1993, 40, 641. (d) Robertson, J.; Burrows, J. N. Tetrahedron Lett. 1994, 35, 3777. 15. Jackon, R. A. J. Organomet. Chem. 1979, 166, 17. 16. (a) Curran, D. P. Synlett 1991, 63. (b) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 4; pp779. (c) Jasperse, C. P.; Curran, D. P.; Fevig, T. L. Chem. Rev. 1991, 91, 1237. (d) Ilhyong, R.; Noboru, S. Chem. Rev. 1996, 96, 177. 17. Curran, D. P.; Rakiewics, D. M. J. Am. Chem. Soc. 1985, 107, 1448. 18. Kilburn, J. D. Tetrahedron Lett. 1990, 31, 2193. 19. Zhou, S.-Z.; Bommezijn, S.; Murphy, J. A. Org. Lett., 2002, 4, 443. 20. Sha, C.-K.; Lee, F.-K.; Chang, C.-J. J. Am. Chem. Soc. 1999, 121, 9875. 21. 唐國祥, 國立台灣大學碩士論文, 1992. 22. Tsai, Y.-M.; Tang, K.-H.; Jiaang, W.-T. Tetrahedron Lett. 1993, 34, 1306. 23. 林其鋒, 國立台灣大學碩士論文, 2002. 24. Carey, F. A.; Sundberg, R. J. Advenced Organic Chemistry A, 3rd, pp684, Plenum: New York and London, 1993. 25. 張聖岳, 國立台灣大學碩士論文, 1996. 26. Chang, S.-Y.; Jiaang, W.-T. ; Cherng, C.-D.; Tang, K.-H.; Huang, C.-H.; Tsai, Y.-M. J. Org. Chem. 1997, 62, 9089. 27. (a) Keiji, T.; Mitsuaki, I.; Hiroshi, K.; Aya, H.; Masaya, N. Tetrahedron Lett. 2001, 42, 3607. (b) Liu, C.; Sowa Jr, John R. Tetrahedron Lett. 1996, 37, 7241. (c) Mori, M.; Washioka, Y.; Urayama, T.; Yoshiura, K.; Chiba, K.; Ban, Y. J. Org, Chem. 1983, 48, 4058. (d) Kropp, P.-J.; McNeely, S.-A.; Davis, R.-D. J. Am. Chem. Soc. 1983, 23, 6907. (e) Campbell, J.-R.; Pross, A.; Sternhell, S. Aust J. Chem. 1971, 24, 1425.(f) Sherred, S.A.; Bergmaw, R.G. J. Am. Chem. Soc. 1971, 93, 1925. 28. Magnus, P.; Exon, Christopher, Albaugh-Robertson, Pamela. Tetrahedron 1985, 24, 5861. 29. Maeyamn, K. ; Okumurn, C. ; Yonezawa, N. Synth. Commun. 2002, 32, 3159. 30. (a)Marshall, F. J.; Cannon, W. N. J. Org. Chem. 1956, 21, 245. (b) Maevel, C. S.; Hager, F. D. Org. Syntheses, Coll. Vol.Ι, 248 (1941). (c) Renfrom, W. B.; Renfrow, A. J. Am. Chem. Soc. 1946, 68, 1801. 31.(a) U. Kruerke, Chem. Ber., 1962, 95, 174. (b) Jung. M.-E.; Lyster, M. A. J. Am. Chem. Soc. 1977, 99, 968. 32. Satoh, T.; Kumagawa, T.; Sugimoto, A.; Yamakawa, K. Bull. Chem. Soc. Jpn. 1987, 60, 301. 33. Murry, J. E.; Wong, G.-B. Synth. Commun. 1972, 2, 389. 34. (a) Herbert S.; William S. J. Org. Chem. 1955, 20, 1458. (b) Pertet A. S. Smith; Jerome P. Horwitz. J. Am. Chem. Soc. 1949, 71, 3418. 35. Meta, E. G.; Maccarett, O. A. Tetrahedron Lett. 1988, 29, 6893. 36. March, J. Advance Organic Chemistry; 4th, pp465. Wiley: New York, 1992. 37. Brook, A. G.; Duff, J. M.; Jones, P. F.; Davis, N. R.; J. Am. Chem. Soc. 1967, 89, 431. 38. Corey, E. J.; Seebach, D.; Freedman, R. J. Am. Chem. Soc. 1967, 89, 434. 39. Kulkarni, S. U.; Patil, V. D. Heterocycles 1982, 18, 163. 40. Trost, B. M. ; Dumas, J. ; Villa, M. J. Am. Chem. Soc. 1992, 114, 9836. 41. Corey, E.-J.; Fuchs, P.-L. Tetrahedron Lett. 1972, 36, 3769. 42. Hayford, A.; Kaloko, J.; Jr., Salwa El-Kazaz,; Bass, G.; Harrison, C.; Corprew, T. Org. Lett. 2005, 7, 2671. 43. (a) Chappell, M. D.; Harris, C. R.; Kuduk, S. D.; Balog, A.; Wu, Z.; Zhang, F.; Lee, C.-B.; Stachel, S. J.; Danishefsky, S. J.; Chou, T.-C.; Guan Y. J. Org. Chem. 2002, 67, 7730. (b) Kabalka, G. W.; Shoup, T. M.; Goudgaon, N. M. J. Org. Chem. 1989, 54, 5930. (c) Corminboeuf, O.; Overman, L. E.; Pennington, L. D. Org. Lett. 2003, 5 , 1543. 44. Fraster F. F.; Lee F.; Ramazan, A.; Yong, T. J. Org. Chem. 2001, 61, 6502. 45. Tom, J. H.; Soongyu, C.; Viresh H. R. Org. Lett. 2001, 3, 3615. 46. (a) Ohira, S. Synth. Commun. 1989, 19, 561. (b) Muller, S.; Liepold, B; Roth, G. J.; Bestmann, H. J. Synlett 1996, 521.(a) Roth, G. J., Liepold, B., Mueller, S. G., Bestmann, H. J. Synthesis 2004, 59. 47. (a) D’Haenens, C.; Vandewalle. Synth. Commun. 1984, 14, 155. (b) Brown, D. G.; Velthuisen, E. J.; Commerford, J. R.; Brisbois, R. G.; Hoye, T. R. J. Org. Chem. 1996, 61, 2540. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/29800 | - |
dc.description.abstract | 本篇論文是利用末端帶有烯基碘的矽基酮為自由基的起始物,在主碳鏈上引入末端含不飽和鍵的支鏈,希望達到連繼性的環化反應。此一環化體系的主體用矽基酮這個官能基,環化後的氧自由基透過Brook重排避免開環以達環化。以烯基碘產生烯基自由基,與矽基酮環化及重排之後得到的是一個烯基自由基,因此我們的挑選最先是採用末端炔矽基,之後也改變為不同的不飽合鍵,以利於達成連繼性環化反應的雙環產生。 | zh_TW |
dc.description.provenance | Made available in DSpace on 2021-06-13T01:19:23Z (GMT). No. of bitstreams: 1 ntu-96-R94223060-1.pdf: 5805781 bytes, checksum: fce0c2edb4868a0e2db6ff9483329643 (MD5) Previous issue date: 2007 | en |
dc.description.tableofcontents | Ⅰ 口試委員會審書
Ⅱ 謝誌 Ⅲ 摘要 Ⅳ 簡語對照表 Ⅴ 緒論 1 Ⅵ 結果與討論 A. 含烯基碘之矽基酮的製備與環化研究 9 B. 含烯基碘之矽基酮的第二合成策略與環化研究 19 C. 含烯基的矽基酮製備與環化研究 29 D. 含烯基苯的矽基酮製備與環化研究 33 E. 增加碳數的矽基酮環化反應 37 Ⅶ 結論 41 Ⅷ 實驗部分 42 Ⅸ 參考文獻 62 Ⅹ 附錄:1H與13C核磁共振光譜 67 | |
dc.language.iso | zh-TW | |
dc.title | 烯基自由基與矽基酮的連繼性環化反應研究 | zh_TW |
dc.title | The Study of Tandem Radical Cyclization of Vinyl Radical with Acylsilanes | en |
dc.type | Thesis | |
dc.date.schoolyear | 95-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 周善行,邱勝賢 | |
dc.subject.keyword | 矽基酮,自由基,連繼性,環化, | zh_TW |
dc.subject.keyword | acylsilane,radical,tandem,cyclization, | en |
dc.relation.page | 66 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2007-07-19 | |
dc.contributor.author-college | 理學院 | zh_TW |
dc.contributor.author-dept | 化學研究所 | zh_TW |
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