簡易檢索 / 詳目顯示

研究生: 薛朋雨
Peng-Yu Hsueh
論文名稱: 有機過渡金屬鐵羰基錯合物在有機合成上的應用
Applications of transition Iron-tricarbonyl complexes in organic syntheses
指導教授: 葉名倉
Yeh, Ming-Chang
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2001
畢業學年度: 89
語文別: 中文
中文關鍵詞: 有機過渡金屬有機合成
英文關鍵詞: transition Iron-tricarbonyl complexes, organic syntheses
論文種類: 學術論文
相關次數: 點閱:186下載:0
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
  • 本論文共分成三部份:
    以三羰基鐵活化後的共軛雙烯,在25℃下,碳的親核性試劑加成到(h4-1,3雙烯)三羰鐵錯合物後,所得的中間體與Davis reagent反應,在閉環系統中以得到C-5位置親核取代的雙烯鐵錯合物為主;而開環系統則以得到終端位置親核取代的雙烯鐵錯合物為主。以有機矽陰離子為親核性試劑與雙烯三羰鐵錯合物進行加成反應,再以Davis reagent終止反應所得到的產物,亦保持原本雙烯三羰鐵的構造;然而以三氟醋酸或溴為親電子性試劑所得到的產物則可得到一系列的有機矽化物。
    利用C-2位置帶酯基的(h4-雙烯)三羰鐵錯合物,在25℃下與二異丙基胺鋰(LDA),進行分子內親核性反應,其反應機構為親核性試劑攻擊(h4-雙烯)三羰鐵錯合物的C-2位置上,造成碳-氧鍵斷裂離去,得到γ-內酯的產物;而C-2位置帶氰基的(h4-雙烯)三羰鐵錯合物,在-78℃或25℃下,進行相同的親核性反應,得到一組非鏡像異構物。
    利用C-2位置帶(1S)-(+)-樟腦磺酮酸為光學輔助劑的開環雙烯化合物,與九羰基二鐵進行錯合反應,由於樟腦磺酮酸的立體效應及酮基的引導作用,使三羰鐵由特定方向與雙烯錯合,可得到非鏡像異構物超越值(de值)>99%的異構物;改以(1R)-(-)-樟腦磺酮酸為光學輔助劑,可得到相對應的鏡像產物,其de值亦大於99%的非鏡像異構物,其立體結構可由 X-ray 繞射結構解析得知。

    The addition of carbon nucleophiles at 25℃ to (h4-1,3-cyclohexadiene)Fe(CO)3 complex followed by hydride abstraction with Davis reagent produces C-5 substituted (h4-1,3-cyclohexadiene)Fe(CO)3 complexes as the major products. With acyclic diene-
    iron complexes, the addition gave predominantly terminal nucleophilic-substituted (h4-
    1,3-diene)Fe(CO)3 complexes. The silicon anion (LiSiMe2Ph) is capable of addition and afford silicon-substituted iron-complex. The reaction path is similar to that of carbon nucleophiles. Quenching the reactive intermediate with trifluoroacetic acid or bromines generated organosilicon compounds.
    Intramolecular addition of ester enolate to iron-complex with an ether linkage at the C-2 position of the diene generates g-lactones as the major product. The reaction involved first addition/elimination followed by intramolecular transesterfication to give the g-lactones.
    Complexation of acyclic dienes, carrying a (1S)-(+)-ketopinoxy as the chiral auxiliary, with Fe2(CO)9 proceeds in a completely diastereoselective fashion to afford diene-iron complexes in moderate yields. When (1R)-(-)-ketopinoxy was used as the chiral auxiliary, the opposite enantioisomeric complexes are isolated as a single diastereomer in comparable yield and specific rotation. The stereochemistry of chiral acyclic diene-iron complexes is determined by single-crystal X-ray methods.

    第一章 緒論 1 第二章 (h4-雙烯)三羰鐵錯合物與親核試劑之加成反應 2.1 前言 2.1.1 (h3-丙烯)三羰鐵陰離子錯合物之反應 15 2.1.2 Davis reagent在有機合成的應用 23 2.1.3 矽陰離子在有機合成的應用 29 2.2 結果與討論 2.2.1 (h3-丙烯)三羰鐵陰離子錯合物與Davis reagent反應 40 2.2.2 矽陰離子與三羰鐵錯合物反應 52 2.3 結論 65 第三章 C-2位置帶官能基之(h4-雙烯)三羰鐵錯合物分子內反應 3.1 前言 67 3.2 結果與討論 3.2.1 C-2位置帶官能基之(h4-雙烯)三羰鐵錯合物的製備 71 3.2.2 雙烯三羰鐵錯合物之分子內異構化反應 74 3.2.3 C-2位置帶官能基之(h4-雙烯)三羰鐵錯合物的延伸反應 83 3.3 結論 87 第四章 以樟腦酮菘酸為光學輔助劑,合成具掌性之三羰鐵錯合物 4.1 前言 88 4.2 結果與討論 4.2.1 製備C-2位置帶光學輔助基之開環雙烯化合物 114 4.2.2 非鏡像異構選擇性反應 117 4.3 結論 124 第五章 實驗部份 5.1 分析儀器及基本實驗操作 125 5.2 實驗部份及光譜數據 5.2.1 一般實驗程序 127 5.2.2 (h3-丙烯)三羰鐵陰離子以Davis reagent為親電子試劑之反應 130 5.2.3 雙烯三羰鐵錯合物與矽陰離子的加成反應 148 5.2.4 C-2位置帶官能基之開環三羰鐵錯合物之加成反應 163 5.2.5 C-2位置帶官能基之閉環三羰鐵錯合物之加成反應 175 5.2.6 C-2 位置帶官能基之(h4-雙烯)三羰鐵錯合物的延伸反應 185 5.2.7 樟腦酮菘酸的製備 189 5.2.8 合成具有光學活性的雙烯分子 191 5.2.9 具有光學活性的雙烯分子與Fe2(CO)9錯合 194 第六章 參考文獻 215

    1. a) Welker, M. E. Chem. Rev. 1992, 92, 97.
    b) Collman, J. P. Acc. Chem. Res. 1975, 8, 342.
    2. Herndon, J. W. J. Am. Chem. Soc. 1987, 109, 3165.
    3. Marsi, M.; Rosenblum, M. J. Am. Chem. Soc. 1984, 106, 7264.
    4. Reihlen, H.; Gruhl, A.; Von Hessling, G.; Pfrengle, O. Liebigs. Ann. Chem. 1930, 482, 161.
    5. Yeh, M. C. P.; Chou, T-s., Tso, H-H.; Tasi, C-Y. J. Chem. Soc., Chem. Commun. 1990, 897.
    6. Fleckner, H.; Grevels, F-W.; Hess, D. J. Am. Chem. Soc. 1984, 106, 2027.
    7. Colson, P.J.; Franck-Neumann, M.; Sedrat, M. Terahedron Lett. 1989, 30, 2393.
    8. Stark, K.; Lancaster, J. E.; Murdoch, H. D.; Weiss, E. Z. Naturforsch. 1964, 19b, 284.
    9. Howell, J. A. S.; Johnson, B. F. G.; Josty, P. L.; Lewis, J. J. Organomet. Chem. 1972, 39, 329.
    10. a) Knölker, H. J.; Gonser, P. Synlett 1992, 517.
    b) Knölker, H. J.; Gonser, P.; Jones, P. G. Synlett 1993, 841.
    c) Knölker, H. J.; Ahrens, B.; Gonser, P.; Heininger, M.; Jones, P. G. Terahedron. 2000, 56, 2259.
    11. Barton, D.H. R.; Gunatilaka, A. A. L.; NaKanishi, I.; Patin, H; Widdowson, D. A.; Worth, B. R. J. Chem. Soc., Perkin Trans. 1, 1976, 821.
    12. a) Thompson, D.J. J. Organometal. Chem. 1976, 108, 381.
    b) Shro, Y.; Hazum, E. J. Chem. Soc., Chem. Commun. 1974, 336.
    c) Alper, H. J. Organomet. Chem. 1975, 96, 95.
    d) Franck-Neumann, M.; Martina, D. Terahedron Lett. 1975, 1759.
    e) Pearson, A. J. J. Chem. Soc., Perkin Trans. 1, 1977, 2069.
    f) Emerson, G.F.; Mahler, J.E.; Kochher, R.; Pettit, R. J. Org. Chem. 1964, 29, 3620.
    g) Mauldin, C.H.; Biehl, E. R.; Reeves, P. C. Terahedron Lett. 1972, 2955.
    h) Coery, E. J.; Monet, G. J. Am. Chem. Soc. 1973, 95, 7185.
    i) Kern, J. M.; Martina, D.; Heitz, M. T. Terahedron Lett. 1985, 26, 737.
    j) Franck-Neumann, M.; Heita, M. P.; Martina, D. Terahedron Lett. 1983, 24, 1615.
    13. Birch, A.J.; Kelley, L. F.; Narula, A. S. Tetrahedron 1982, 38, 1813.
    14. Franck-Neumann, M.; Martina, D. Tetrahedron Lett. 1982, 23, 3493.
    15. a) Hunt, D. F.; Lillya, C. P.; Rausch, M. D.; J. Am. Chem. Soc. 1968, 90, 2561.
    b) Falkowski, D. R.; Hunt, D. F.; Lillya, C. P.; Rausch, M. D.; J. Am. Chem. Soc. 1967, 89, 6387.
    c) Clinton, N. A.; Lillya, C. P. J. Am. Chem. Soc. 1970, 92, 3065.
    16. Yeh, M. C. P.; Chang, S.-C.; Chang, C.-J. J. Organomet. Chem. 2000, 599, 128.
    17. Yeh, M. C. P.; Tau, S. I. J. Chem. Soc., Chem. Commun. 1992, 13.
    18. a) For a review, see: Pearson, A. J. Acc. Chem. Res. 1980, 13, 463.
    b) Mahler, J. E.; Pettit, R. J. Am. Chem. Soc. 1963, 85, 3955.
    19. Yeh, M. C. P.; Hwu, C.-C.; J. Organomet. Chem. 1991, 419, 341.
    20. Semmelhack, M. F.; Herndom, J. W.; Spring, J. P. J. Am. Chem. Soc. 1983, 105, 2497.

    21. Semmelhack, M. F.; Herndom, J. W. Organometallics 1983, 105, 2497.
    22. Semmelhack, M. F.; H. T. M. J. Am. Chem. Soc. 1984, 106, 2715.
    23. Le, Hahn. M. T. Ph. D. Dissertation. Princeton University. 1985.
    24. a) Reberts, B. W.; Wong, J. J. Chem. Soc., Chem. Commun. 1977, 20.
    b) Reberts. B. W.; Ross, M.; Wong, J. J. Chem. Soc., Chem. Commun. 1980, 428.
    25. Reviews:a) Davis, F. A.; Sheppard, A. C. Tetrahedron 1989, 45, 5703.
    b) Davis, F. A.; Chen, B.-C. Chem. Rev. 1992, 92, 919.
    26. a) Davis, F. A.; Rizvi, S. Q. A.; Ardecky, R.; Gosciniak, D. J.; Friedman, A. J.;
    Yocklovich, S. G. J. Org. Chem. 1980, 45, 1650.
    b) Davis, F. A.; Billmer, J. M.; Gosciniak, D. J.; Towson, J. C.; Bach, R. D. J. Org. Chem. 1986, 51, 4240.
    c) Davis, F. A.; Jenkins, Jr. R. H.; Yocklovich, S. G. Terahedron Lett. 1978, 5171.
    27. Zajac, Jr.; W. W.; Walters. T. R. J. Org. Chem. 1988, 53, 5856.
    28. a) Davis, F. A.; Abdul-Malik, N. F.; Awad, S. B.; Harakal, M. E. Terahedron
    Lett. 1981, 917.
    b) Davis, F. A.; Nadir, U. K.; Kluger, E. W. J. Chem. Soc., Chem. Commun. 1977, 25.
    29. a) Davis, F. A.; Wei, J.; Sheppard, A. C.; Gubernick, S. Terahedron Lett. 1987,
    5115.
    b) Davis, F. A.; Vishwaka, L. C.; Billmers, J. G.; Finn, J. J. Org. Chem. 1984, 49, 3241.
    c) Evans, D. A.; Morrissey, M. M.; Dorow, R. L. J. Am. Chem. Soc. 1985, 107, 4346.
    30. Salim, M.; David, M.; Edwin, H. R.; Nicholas J. T.; Sandra, M.; Gary, I. D. J. Am. Chem. Soc. 1997, 119, 1159.
    31. Davis, F. A.; Vishwakarma, L. C.; Stringer, O. D. Org. Syn. 1987, 66, 201.
    32. a) Hudrlik, P. F.; Peterson, D. J. Am. Chem. Soc. 1975, 97, 1464.
    b) Hudrlik, P. F.; Peterson, D.; Rona, R. J. J. Org. Chem. 1975, 40, 2263.
    33. For a review, see a) Hatanaka, Y.; Hiyama, T. Synlett 1991, 845. b) Takahashi, K.; Minami, T.; Ohara, Y.; Hiyama, T. Terahedron Lett. 1993, 34, 8263.
    34. a) Fleming, I.; langley, J. A. J. Chem. Soc., Perkin Trans. 1, 1981, 1421.
    b) Jeulins, P. R.; Gut, R.; Wetter, H.; Eschenmoser, A. Helv. Chim. Acta. 1979, 62, 1922.
    35. a) Feleming, I.; Henning, R.; Parker, D. C.; Plaut, H. E.; Sanderson, P. E. J. J.
    Chem. Soc., Perkin Trans. 1, 1995, 317.
    b) Tamao, K.; Kakui, T.; Akita, M.; Iwahara, T.; Kanatani, R.; Yoshida, J.;
    Kumada, M. Tetrahedron 1983, 39, 983.
    36. a) Fleming, I.; Sanderson, P. E. J. Terahedron Lett. 1987, 28, 4229.
    b) Fleming, I. Appl. Chem., 1988, 60, 71.
    c) Fleming, I.; Henning, R.; Plaut, H. J. Chem. Soc., Chem. Commun. 1984, 29.
    37. a) Sakurai, H.; Okada, A.; Kira, M.; Yonezawa, K. Terahedron Lett. 1971, 19,
    1511.
    b) W. Clark Still. J. Org. Chem. 1976, 18, 3063.
    38. Rahman, N. A.; Fleming, I.; Zwicky, A. B. J. Chem. Res. (S), 1922, 292; J. Chem. Res. (M), 2041.

    39. Fleming, I.; Roberts, R. S.; Smith, S. C. J. Chem. Soc., Perkin Trans. 1, 1998, 1209.
    40. a) Wittenberg, D.; Wu, T. C.; Gilman, H. J. Org. Chem. 1959, 24, 1349.
    b) Stork, G.; Hudrlik, P. F. J. Am. Chem. Soc. 1968, 90, 4464.
    41. Fleming, I.; Saito, S.; Shimada, K.; Yamamoto, H.; Marigorta, E. M. J. Chem. Soc., Chem. Commun. 1997, 1299.
    42. Fleming, I.; Newton, T. W.; Roessler, F J. Chem. Soc., Perkin Trans. 1, 1981, 2527.
    43. Lipshutz, B. H.; Sclafani, J. A.; Takanaami, T. J. Am. Chem. Soc. 1998, 120, 4021.
    44. a) Krűger, C.; Tsay, Y.-H. J. Organometal. Chem. 1971, 33, 59.
    b) Jaenicke, O.; Kerber, R. C.; Kirsch, P.; Koerner von Gustorf.; Rumin, R. J.
    Organomet. Chem. 1980, 187, 361.
    c) Lumbroso, H.; Bertin, D. M. J. Organomet. Chem. 1976, 108, 33.
    45. a) Pearson, A. J.; Yoon, J. Terahedron Lett. 1985, 26, 2399.
    b) Birch, A. J.; Pearson, A. J. Terahedron Lett. 1975, 28, 2379.
    c) Birch, A. J.; Jenkins, I. D.; Liepa, A. J. Terahedron Lett. 1975, 21, 1723.
    46. Yeh, M. C. P.; Sheu, B.-A.; Fu, H.-W.; Tau, S.-I.; Chuang, L.-W. J. Am. Chem. Soc. 1998, 120, 4021.
    47. Yeh, M. C. P.; Chuang, C.-W.; Hwu, C.-C.; Sheu, J.-M.; Row, L.-C. Organometallics 1995, 14, 3396.
    48. 賴明良, 碩士論文, 國立台灣師範大學, 1996.
    49. Wang, J. L.; Ueng, C. H.; Cheng, S. J.; Yeh, M. C. P. Organometallics 1994, 13, 4453.
    50. Yeh, M. C. P.; Wang, F. C.; Tu, J. J.; Chang, S. C.; Chou, C. C.; Liao, J. W. Organometallics 1998, 26, 5656.
    51. Pearson, A. J. Acc. Chem. Res. 1980, 13, 463.
    52. Birch, A. J.; Kelly, L. F.; Weerasuria, D. V. J. Org. Chem. 1988, 53, 278.
    53. Takemoto, Y.; Yoshikawa, N.; Baba, Y.; Iwata, C.; Tanaka, T.; Ibuka, T.; Ohishi, H. J. Am. Chem. Soc. 1999, 121, 9143.
    54. Birsh, A. J.; Bandara, B. M. R. Terahedron Lett. 1980, 21, 2981.
    55. Bandara, B. M. R.; Birch, A. J.; kelly, L. F.; Khor, T. C. Terahedron 1980, 24, 2491.
    56. Pinsard, P.; Lellouche, J.-p.; Beaucourt, J.-p.; Grée, R. Terahedron Lett. 1990, 31, 1141.
    57. Franck-Neumann, M.; Briswalter, C.; Chemla, P.; Martina, D. Synlett 1990.637.
    58. Pearson, A. J.; Chang, K.; Mcconville, D. B.; Youngs, W. J. Organometallics 1994, 13, 4.
    59. Schmalz, H.-G.; Heßler, E.; Bats, J. W.; Dürner, G. Terahedron Lett. 1994, 26, 4543.
    60. Ong, C. W.; Hsu, R. H. Organometallics 1994, 13, 3952.
    61. Ong, C. W.; Hung, C. S.; Chang, T. H. Organometallics 1996, 15, 4334.
    62. Alcock, N. W.; Crout, D. H. G.; Henderson, C. M.; Thomas, S. E. J. Chem. Soc., Chem. Commun. 1988, 746.
    63. Howell, J. A. S.; Palin, M. G. Terahedron Asymmetry. 1993, 4, 1241.
    64. Knölker, H.-J. Chem. Rev. 2000, 100, 2941.
    65. Knölker, H.-J.; Hermann, H. Angew. chem., Int. Ed. Engl. 1996, 3, 341.
    66. Tsai, M.-S.; Rao, U. N.; Hsueh, P.-Y.; Yeh, M. C. P. Organometallics 2001, 20, 289.
    67. a) Varkevisser, F. A.; Kokke, W. C. M. C. J. Org. Chem. 1974, 39, 1653.
    b) Fischer, N.; Opitz, G. Org. Syntheses. 1973, 5, 877.
    c) Knox, L. H.; Bartlett, P. D. Syntheses. 1973, 5, 689.
    68. Xiang, Y. B.; Snow, K.; belley, M. J. Org. Chem. 1993, 58, 993.
    69. Oppolzer, W.; Dupuis, D. Terahedron Lett. 1985, 26, 5437.
    70. Oppolzer, W.; Pedrosa, R.; Moretti, R. Terahedron Lett. 1986, 27, 831.
    71. Ahn, K. H.; Lee, S.; Lim, A. J. Org. Chem. 1992, 57, 5065.
    72. Oppolzer, W.; Radinov, R. N. Terahedron Lett. 1988, 29, 5645.
    73. Howell, J. A. S. J. Organomet. Chem. 1984, 266, 83.

    無法下載圖示
    QR CODE