簡易檢索 / 詳目顯示

研究生: 黃孟婷
Huang, Meng-Ting
論文名稱: 手性硫化物於催化性氮丙啶化反應之應用
(Thiolan-2-yl)diphenylmethanol-catalyzed asymmetric aziridination
指導教授: 陳榮傑
Chein, Rong-Jie
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2013
畢業學年度: 102
語文別: 中文
論文頁數: 79
中文關鍵詞: 鋶偶極體亞胺氮丙啶立體選擇性反應有機催化劑
英文關鍵詞: sulfur-ylide, N-diphenylphosphinic imine, diaryl aziridine, enantioselective reaction, organocatalyst
論文種類: 學術論文
相關次數: 點閱:155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
  • 以市售的5-溴基戊酸乙脂作為起始物,經由四步驟合成而得硫化物1b-1d,接著再一步驟得到硫化物衍生物2b-2d。接著,以硫化物2b-2d作為催化劑進行不對稱氮丙啶反應之應用。

    A novel chiral tetrahydrothiophene derivative 2b-2d was obtained from commercially available 5-Bromovalerate through a 5-steps synthetic route. We demonstrated the application of catalytic and asymmetric process for aziridination mediated by sulfur ylides.

    誌謝  i 中文摘要 ii Abstract iii 目錄 iv 圖目錄 vi 表目錄 viii 第一章 緒論 1 1-1 氮丙啶 (Aziridine) 1 1-1-1 氮丙啶化反應(Aziridination) 4 1-1-2 利用鋶偶極體進行不對稱氮丙啶化反應 9 1-1-3 合成應用 16 1-2 配位基(Thiolan-2-yl)diphenylmethanol簡介 17 1-2-1 (R)- (Thiolan-2-yl)diphenylmethanol合成路徑及其應用 18 1-2-2 (S)- (Thiolan-2-yl)diphenylmethanol合成路徑及其應用 21 第二章 結果與討論 23 2-1 硫化物 23 2-2-1 硫化物1b之製備 23 2-2-2 硫化物1c之製備 24 2-2-3 硫化物1d之製備 25 2-2-4 硫化物衍生物之製備 27 2-2 氮丙啶 28 2-2-1 保護基之篩選 28 2-2-2 催化劑之篩選 32 2-2-3 溶劑之篩選 34 2-2-4 鹼之篩選 35 2-2-5 添加劑之篩選 36 2-2-6 不同取代基的氮丙啶 37 2-2-7 反應機構 42 第三章 結論 43 第四章 實驗部分 44 第五章 文獻參考 78

    [1] I. D. G. Watson, L. Yu, A. K. Yudin, Acc. Chem. Res. 2006, 39, 194-206.
    [2] D. A. Evans, M. M. Faul, M. T. Bilodeau, B. A. Anderson, D. M. BarneslC, J. Am.
    Chem. Soc. 1993, 115, 5328-5230.
    [3] W. Wulff, Y. Zhang, Z. Lu, Synlett 2009, 2009, 2715-2739.
    [4] K. B. Hansen, N. S. Finney, E. N. Jacobsen, Angew. Chem. Int. Ed. Engl 1995, 34,
    676-678.
    [5] D. Morton, D. Pearson, R. A. Field, R. A. Stockman, Org. Lett. 2004, 6, 2377-
    2380.
    [6] A.-H. Li, L.-X. Dai, X.-L. Hou, M.-B. Chen, J. Org. Chem. 1996, 61, 4641-4648.
    [7] A.-H. Li, Y.-G. Zhou, L.-X. Dai, X.-L. Hou, L.-J. Xia, L. Lin, Angew. Chem. Int.
    Ed. 1997, 36, 1317-1319.
    [8] A.-H. Li, L.-X. Dai, X.-L. Hou, Y.-Z. Huang, F.-W. Li, J. Org. Chem 1996, 61,
    489-493.
    [9] O. Illa, M. Arshad, A. Ros, E. M. McGarrigle, V. K. Aggarwal, J . Am. Chem. Soc.
    2010, 132, 1828-1830.
    [10] T. Saito, M. Sakairi, D. Akiba, Tetrahedron Lett. 2001, 42, 5451-5454.
    [11] T. Saito, D. Akiba, M. Sakairi, S. Kanazawa, Tetrahedron Lett. 2001, 42, 57-59.
    [12] Y. Gui, S. Shen, H.-Y. Wang, Z.-Y. Li, Z.-Z. Huang, Chem. Lett. 2007, 36, 1436-
    1437.
    [13] a)V. K. Aggarwal, A. Thompson, R. V. H. Jones, M. C. H. Standen, J. Org. Chem.
    1996, 61, 8336-8369;
    b)V. K. Aggarwal, M. Ferrara, C. J. O'Brien, A. Thompson, R. V. H. Jones, R.
    Fieldhouse, J. Chem. Soc., Perkin Trans. 1 2001, 1635-1643.
    [14] V. K. Aggarwal, E. Alonso, G. Fang, M. Ferrara, G. Hynd, M. Porcelloni, Angew.
    Chem. Int. Ed. 2001, 40, 1433-1436.
    [15] V. K. Aggarwal, J.-L. Vasse, Org. Lett. 2003, 5, 3987-3990.
    [16] E. J. Corey, R. K. Bakshi, S. Shibata, J . Am. Chem. Soc. 1987, 109.
    [17] a)E. J. Corey, T. Shibata, T. W. Lee, J . Am. Chem. Soc. 2002, 124, 3808-3809;
    b)K. Sakata, H. Fujimoto, J. Org. Chem. 2013, 78, 3095-3103;
    c)J. N. Payette, H. Yamamoto, Angew. Chem. Int. Ed. Engl. 2009, 48, 8060-8062;
    d)D. Liu, E. Canales, E. J. Corey, J . Am. Chem. Soc. 2007, 129, 1498-1499.
    [18] Y. Hayashi, H. Gotoh, T. Hayashi, M. Shoji, Angew. Chem. Int. Ed. Engl. 2005,
    44, 4212-4215.
    [19] I. Shiina, K. Konishi, Y.-s. Kuramoto, Chem. Lett. 2002, 164-165.
    [20] M. Yamakawa, R. Noyori, Organometallics 1999, 18, 128-133.
    [21] H. Y. Wu, C. W. Chang, R. J. Chein, J. Org. Chem. 2013, 78, 5788-5793.
    [22] D. J. Vyas, R. Fröhlich, M. Oestreich, Org. Lett. 2001, 13, 2094–2097.
    [23] G. Bashiardes, G. J. Bodwell, S. G. Davies, J. Chem. Soc., Perkin Trans. 1 1993,
    1, 459-469.
    [24] B. Ritzen, M. C. M. van Oers, F. L. van Delft, F. P. J. T. Rutjes, J. Org. Chem.
    2009, 74, 7548-7551.
    79
    [25] Z.-X. Wang, Y. Tu, M. Frohn, J.-R. Zhang, Y. Shi, J. Am. Chem. Soc. 1997, 119,
    11224-11235.
    [26] K.-C. Liu, B. R. Shelton, R. K. Howe, J. Org. Chem. 1980, 45, 3916-3918.
    [27] A. R. Hajipour, I. Mohammadpoor-baltork, K. Nikbaghat, G. Imanzadeh, Synth.
    Commun. 1999, 29, 1697-1701.
    [28] C. L. Allen, S. Davulcu, J. M. J. Williams, Org. Lett 2010, 12, 5096-5099.
    [29] G. W. Zamponi, S. C. Stotz, R. J. Staples, T. M. Andro, J. K. Nelson, V. Hulubei,
    A. Blumenfeld, N. R. Natale, J. Med. Chem. 2003, 46, 87-96.
    [30] R. Ballini, L. Barboni, P. Filippone, Chem. Lett. 1997, 475-476.
    [31] D. A. Colby, R. G. Bergman, J. A. Ellman, Org. Lett. 2010, 110, 624-655.
    [32] C. Lauzon, J. N. Desrosiers, A. B. Charette, J. Org. Chem. 2005, 70, 10579-10580.
    [33] S. Banerjee, J. A. Groeper, J. M. Standard, S. R. Hitchcock, Tetrahedron:
    Asymmetry 2009, 20, 2154-2161.
    [34] H. Kinoshita, O. J. Ingham, W. W. Ong, A. B. Beeler, J. John A. Porco J. Am.
    Chem. Soc. 2012, 132, 6412-6418.
    [35] A. A. Boezio, J. Pytkowicz, A. Cote, A. B. Charette, J. Am. Chem. Soc. 2003, 125,
    14260-14261.
    [36] T. Yukawa, B. Seelig, Y. Xu, H. Morimoto, S. Matsunaga, A. Berkessel, M.
    Shibasaki, J. Am. Chem. Soc. 2010, 132, 11988-11992.
    [37] P. Pinho, P. G. Andersson, Tetrahedron 2001, 57, 1615-1618.
    [38] R. Appel, H. Mayr, J. Am. Chem. Soc. 2011, 133, 8241-8250.

    無法下載圖示 本全文未授權公開
    QR CODE