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 |
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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.
[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.