研究生: |
黃思穎 Huang, Szu-Ying |
---|---|
論文名稱: |
一價銠金屬催化氮-對甲苯磺醯基之1,2‐二氫喹啉進行不對稱氫芳基化反應 Rhodium(I)-Catalyzed Asymmetric Hydroarylation of N-Tosyl 1,2-Dihydroquinolines |
指導教授: |
吳學亮
Wu, Hsyueh-Liang |
學位類別: |
碩士 Master |
系所名稱: |
化學系 Department of Chemistry |
論文出版年: | 2020 |
畢業學年度: | 108 |
語文別: | 中文 |
論文頁數: | 226 |
中文關鍵詞: | 鏡像選擇性 、一價銠金屬催化 、氫芳基化反應 、1,2‐二氫喹啉 、2H-色原烯 、四芳基硼鈉試劑 、不對稱加成反應 、掌性 、掌性雙環[2.2.1]雙烯配基 |
英文關鍵詞: | enantioselective, Rhodium(I)-catalyzed, hydroarylation, 1,2-dihydroquinolines, 2H-chromenes, sodium tetraarylborates, asymmetric addition, chiral, chiral bicyclo[2.2.1]diene ligands |
DOI URL: | http://doi.org/10.6345/NTNU202000854 |
論文種類: | 學術論文 |
相關次數: | 點閱:232 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 |
本篇論文探討一價銠金屬試劑與掌性雙環[2.2.1]雙烯配基L2a形成之催化劑,於溫度100 ℃且使用環戊基甲基醚為溶劑,並加入甲醇為添加劑的條件下,催化1,2‐二氫喹啉或2H-色原烯12與四芳基硼鈉13進行不對稱加成反應,得到一系列3號位具芳香基之掌性1,2,3,4-四氫喹啉或3號位具芳香基之掌性色原烷14,產率為10–92%,鏡像超越值為87–99%。此外,利用掌性1,2,3,4-四氫喹啉化合物14mh進行去甲基反應及利用掌性1,2,3,4-四氫喹啉化合物14nn經由宮浦硼酸化 (Miyaura borylation)與氧化反應可合成目標產物雌激素乙型受體促效劑 ((R)-3),前者產率為86%,後者兩個步驟的總產率為52%。
This thesis describes an enantioselective addition of sodium tetraarylborates 13 to 1,2-dihydroquinolines or 2H-chromenes 12 in cyclopentyl methyl ether at 100 ℃ with 5.0 equiv of methanol as an additive in the presence of 3.0 mol % of Rh(I)-catalyst in situ generated from the [RhCl(C2H4)2]2 and chiral bicyclo[2.2.1]heptadiene ligand L2a. The desired products 14 were generated in 10–92% yields with 87–99% ees. In addition, the synthesis of Estrogen receptor β agonist ((R)-3) was achieved by demethylation of compound 14mh in 86% yield. The desired product ((R)-3) was also obtained by Miyaura borylation of compound 14nn followed by oxidation in 52% yield for 2 steps.
1. Teo, S. K.; Colburn, W. A.; Tracewell, W. G. Clin. Pharmacokinet. 2004, 43, 311–327.
2. Sridharan, V.; Suryavanshi, P. A.; Menéndez, J. C. Chem. Rev. 2011, 111, 7157–7259.
3. Kubota, K.; Watanabe, Y.; Ito, H. Adv. Synth. Catal. 2016, 358, 2379–2384.
4. Kong, D.; Han, S.; Zi, G.; Hou, G.-H.; Zhang, J.-X. J. Org. Chem. 2018, 83, 1924–1932.
5. (a) Jian, J.-H.; Hsu, C.-L.; Syu, J.-F.; Kuo, T.-S.; Tsai, M.-K.; Wu, P.-Y.; Wu, H.-L. J. Org. Chem. 2018, 83, 12184–12191. (b) Chang, C.-A.; Uang, T.-Y.; Jian, J.-H.; Zhou, M.-Y.; Chen, M.-L.; Kuo, T.-S.; Wu, P.-Y.; and Wu, H.-L. Adv. Syn. Cat. 2018. (c) Syu, J.-F.; Wang, Y.-T.; Liu, K.-C.; Wu, P.-Y.; Henschke, J. P.; Wu, H.-L. J. Org. Chem. 2016, 81, 10832–10844. (d) Fang, J.-H.; Chang, C.-A.; Gopula, B.; Kuo, T.-S.; Wu, P.-Y.; Henschke, J. P.; Wu, H.-L. Asian J. Org. Chem. 2016, 5, 481 – 485. (e) Gopula, B.; Yang, S.-H.; Kuo, T.-S.; Hsieh, J.-C.; Wu, P.-Y.; Henschke, J. P.; Wu, H.-L. Chem. Eur. J. 2015, 21, 11050 – 11055. (f) Wei, W.-T.; Yeh, J.-Y.; Kuo, T.-S.; Wu, H.-L. Chem. Eur. J. 2011, 17, 11405-11409.
6. Takahashi, M.; Takaya, Y.; Ogasawara, M.; Hayashi, T. J. Am. Chem. Soc. 2002, 124, 50520–5058.
7. Oguma, K.; Satoh, T.; Nomura, M.; Miura, M. J. Am. Chem. Soc. 2000, 122, 10464–10465.
8. Roy, A.; Fukuoka, K.; Fagnou, K.; Martin-Matute, B.; Lautens, M. J. Am. Chem. Soc. 2001, 123, 5358–5359.
9. Saxena, A.; Lam, H.-W. Chem. Sci. 2011, 2, 2326–2331.
10. Dockendorff, C.; Fagnou, K.; Malicki, A.; Lautens, M. Org. Lett. 2002, 4, 1311–1314.
11. Igawa, H.; Murakami, M. Chem. Commun. 2002, 390–391.
12. Panteleev, J.; Menard, F.; Lautens, M. Adv. Synth. Catal. 2008, 350, 2893–2902.
13. So, C.-M.; Hayashi, T. J. Am. Chem. Soc. 2013, 135, 10990–10993.
14. Xing, J.; Zhu, W.; Ye, B.; Lu, T.; Dou, X.; Hayashi, T. ACS. Catal. 2020, 10, 2958––2963.
15. Yang, Q.; Wang, Y.; Luo, S.; Wang, J. Angew. Chem. Int. Ed. 2019, 58, 5343-5347.
16. Umeda, M.; Sakamoto, K.; Nagai, T.; Nagamoto, M.; Ebe, Y.; Nishimura, T. Chem. Commun. 2019, 55, 11876-11879.
17. Ueyama, K.; Tpkunaga, N.; Yoshida, K.; Hayashi, T. J. Am. Chem. Soc. 2003, 125, 11508–11509.
18. Wei, W.-T.; Yeh, J.-Y.; Kuo, T.-S.; Wu, H.-L. Chem. Eur. J. 2011, 17, 11405–11409.
19. Syu, J.-F.; Lin, H.-Y.; Cheng, Y.-Y.; Tsai, Y.-C.; Ting, Y.-C.; Kuo, T.-S.; Janmanchi, D.; Wu, P.-Y.; Henschke, J. P.; Wu, H.-L. Chem. Eur. J. 2017, 23, 14515–14522.
20. Chen, W.; Lin, Z.; Ning, M.; Yang, C.-H.; Yan, X.; Xie, Y.; Shen, X.; Wang, M.-W. Bioorg. Med. Chem. 2007, 15, 5828-5836.
21. Ishiyama, T.; Ishida, K.; Miyaura, N. Tetrahedron. 2001, 57, 9813–9816.
22. Kubota, K.; Watanabe, Y.; Hayama, K.; Ito, H. J. Am. Chem. Soc. 2016, 138, 4338–4341.
23. Tiwari, V. K.; Pawar, G. G.; Das, R.; Adhikary, A.; Kapu, M. Org. Lett. 2013, 15, 3310–3313.
24. Tokuyama, H.; Sato, M.; Ueda, T.; Fukuyama, T. Heterocycles 2001, 54, 105–108.
25. Xu-Xu, Q.-F.; Zhang, X.; You, S.-L. Org. Lett. 2019, 21, 5357–5362.
26. Madugula, S. R. M.; Thallapelly, S.; Bandarupally, J.; Yadav, J. S. US 2007/0123708 A1.
27. Rosenmund, K. W.; Zymalkowski, F.; Schwarte, N. Chem. Ber. 1954, 87, 1229–1235.
28. Theeraladanon, C.; Arisawa, M.; Nishida, A.; Nakagawa, M. Tetrahedron. 2004, 60, 3017–3035.
29. Suresh, V.; Selvam, J. J. P.; Rajesh, K.; Shekhar, V.; Babu, D. C.; Venkateswarlu, Y. Synthesis. 2010, 11, 1763–1765.
30. Wu, Z.-J.; Qian, J.; Wang, P.-C.; Wang, T.-T.; Huang, Z.-Z. CN 103980243 A.
31. Ashooriha, M.; Khoshneviszadeh, M.; Khoshneviszadeh, M.; Moradi, S. E.; Rafiei, A.; Kardan, M.; Emam, S. Bioorganic Chemistry 2019, 82, 414–422.
32. Gopalsamy, A.; Balasubramanian, K. K. J. Chem. Soc. Chem. Commun. 1988, 28–29.
33. Lorena, A.-M.; Martínez, M. M.; Sarandeses, L. A.; Sestelo, J. P. Org. Biomol. Chem. 2015, 13, 379–387.
34. Li, X.; Wang, C.; Song, J.; Yang, Z.; Zi, G.; Hou, G. J. Org. Chem, 2019, 84, 8638−8645.
35. Song, W.; Lynch, J. C.; Shu, X.-Z.; Tang, W. Adv. Synth. Catal. 2016, 358, 2007 – 2011.
36. Rodrigues, N.; Bennis, K.; Vivier, D.; Pereira, V.; Chatelain, F. C.; Chapuy, E.; Deokar, H.; Busserolles, J.; Lesage, F.; Eschalier, A.; Ducki, S. European Journal of Medicinal Chemistry 2014, 75, 391–402.