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研究生: 許晉逢
Syu, Jin-Fong
論文名稱: 利用銠金屬催化反應合成前列腺素以及阿普斯特片
TOTAL SYNTHESES OF PROSTAGLANDINS AND APREMILAST CATALYZED BY RHODIUM CATALYSTS
指導教授: 吳學亮
Wu, Hsyueh-Liang
學位類別: 博士
Doctor
系所名稱: 化學系
Department of Chemistry
論文出版年: 2018
畢業學年度: 106
語文別: 中文
論文頁數: 218
中文關鍵詞: 共軛加成反應銠金屬掌性配基硼酸鏡像超越值
英文關鍵詞: conjugate addition, chiral ligand,, boronic acid, Rh(I)-catalyzed, Enantioselective
DOI URL: http://doi.org/10.6345/DIS.NTNU.DC.054.2018.B05
論文種類: 學術論文
相關次數: 點閱:181下載:0
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  • 本論文研究以一價銠金屬形成之催化劑催化不對稱1,4-加成反應。分為兩部分:第一部分是合成阿普斯特片(Apremilast),第二部分則是合成多種前列腺素。
    一、 銠金屬(I)催化芳香族硼酸對β-酞醯亞胺烯基碸進行不對稱加成反應進而合成阿普斯特片
    利用5 mol %銠金屬與6 mol %掌性雙烯配基L1或L10催化芳香基硼酸對-酞醯亞胺烯基碸化合物進行不對稱芳基加成反應,可以有效合成一系列具有高鏡像選擇性產物。總共有27個例子,產率為13–96%,鏡像超越值為94–99%,並且我們藉由配基的選擇可以控制產物的掌性中心。得到的加成產物經過一步反應後可以得到藥物阿普斯特片(18)。


    二、 銠金屬(I)催化烯基芳香族硼酸對2-環戊烯酮進行不對稱加成反應並應用在合成前列腺素
    此題目主要是探討利用一價銠金屬([RhCl(COD)]2),以甲醇作為溶劑,催化量的氫氧化鉀作為添加劑,以低功率微波(50 W)在30 °C的條件下進行烯基硼酸對具有掌性中心的化合物(129)進行1,4-共軛加成反應,得到單一非鏡像異構物,並可進而合成F型前列腺素(Prostaglandins, PG) dinoprost以及tafluprost (zioptan)。

    共軛加成反應,銠金屬, 掌性配基, 硼酸, 鏡像超越值

    This thesis describes the employment of Rh(I)-catalyzed 1,4-addition reactions and is divided into two topics: the synthesis Apremilast and the preparation of various prostaglandins.
    1. Rh-Catalyzed Enantioselective Arylation of β-Phthalimino Vinylsulfones: The Syntheisis of Apremilast.
    Enantioenriched -amino sulfones were prepared from the Rh-catalyzed asymmetric addition of a range of arylboronic acids to -phthalimide vinyl sulfones in the presence of Rh(I)-catalysts comprising chiral diene ligands L1 and L10 that gave (R) and (S) adduct, respectively. This asymmetric transformation sees its synthetic application in the synthesis of Apremilast.


    2. Rh(I)-Catalyzed 1,4-Conjugate Addition of Alkenylboronic Acids to a Cyclopentenone Useful for the Synthesis of Prostaglandins
    An efficient and trans-diastereoselective Rh(I)-catalyzed 1,4-conjugate addition reaction of alkenylboronic acids and a homochiral (R)-4-silyloxycyclopentenone useful for the synthesis of derivatives of prostaglandins E and F is described for the first time. The reaction functions under mild conditions and is particularly rapid under low power (50 W) microwave irradiation at 30 °C in MeOH in the presence of a catalytic amount of KOH. Under these conditions, 3 mol % of [RhCl(COD)]2 is typically required to produce high yields. This method demonstrats its utility in the synthesis of PGF2α (dinoprost) and tafluprost (zioptan).

    conjugate addition, Rh(I)-catalyzed, chiral ligand, boronic acid, Enantioselective

    目錄 中文摘要 i Abstract iii 謝誌 v 英文縮寫對照表 xiv 第一章:緒論(I) 1 第二章:文獻回顧(I) 19 第三章:掌性雙環[2.2.1]雙烯配基合成 29 第四章:結果與討論 34 4-1 Apremilast之逆合成分析 34 4-2 溶劑與添加劑的效應 35 4-3 配基效應(I) 38 4-4 配基效應(II) 39 4-5 溫度效應 40 4-6 催化劑劑量效應 41 4-7 利用最佳化條件進行一系列硼酸不對稱加成反應(I) 43 4-8 使用cis form的起始物進行不對稱加成反應 45 4-9 利用最佳化條件進行一系列硼酸不對稱加成反應(II) 47 4-10 利用最佳化條件進行一系列硼酸不對稱加成反應(III) 48 4-11 利用最佳化條件進行一系列硼酸不對稱加成反應(IV) 49 4-12 合成應用 50 第五章:絕對立體化學討論 61 第六章:緒論(II) 64 第七章:文獻探討 67 第八章:實驗結果與討論(II) 78 8-1 溶劑效應 80 8-2 溫度效應 82 8-3 添加劑效應 84 8-4 溶劑效應(II) 87 8-5 微波效應 88 8-6 試劑補加效應 91 8-7 α-側鏈效應 92 8-8 硼試劑效應 94 8-9 溫度效應(II) 96 8-10 利用最佳化條件進行一系列不同硼酸的反應 97 8-11 合成曲伏前列素以及比馬前列素前驅物 98 8-12 合成地諾前列素 101 8-13 合成他氟前列素 104 第九章:立體化學探討 106 十、結論 108 第十一章:實驗部分 110 第十二章:參考文獻 212

    (1) Hayashi, T.; Takahashi, M.; Takaya, Y.; Ogasawara, M. J. Am. Chem. Soc. 2002, 124, 5052.
    (2) Kina, A.; Iwamura, H.; Hayashi, T. J. Am. Chem. Soc. 2006, 128, 3904.
    (3) Kina, A.; Yasuhara, Y.; Nishimura, T.; Iwamura, H.; Hayashi, T. Chem. Asian J. 2006, 1, 707.
    (4) Chen, F. -X.; Kina, A.; Hayashi, T. Org. Lett. 2006, 8, 341.
    (5) Senda, T.; Ogasawara, M.; Hayashi, T. J. Org. Chem. 2001, 66, 6852.
    (6) Takaya, Y.; Senda, T.; Kurushima, H.; Ogasawara, M.; Hayashi, T. Tetrahedron: Asymmetry 1999, 10, 4047.
    (7) Brak, K.; Ellman, J. A. J. Org. Chem. 2010, 75, 3147. Pucheault, M.; Darses, S.; Genet, J. -P. Eur. J. Org. Chem. 2002, 21, 3552.
    (8) (a) Pucheault, M.; Darses, S.; Genet, J. -P. Tetrahedron Lett. 2002, 43, 6155. (b) Darses, S.; Genet, J. -P. Eur. J. Org. Chem. 2003, 22, 4313. (c) Molander, G. A.; Figueroa, R. Aldrichimica Acta 2005, 38, 49.
    (9) Navarre, L.; Martinez, R.; Genet, J. -P.; Darses, S. J. Am. Chem. Soc. 2008, 130, 6159.
    (10) (a) Batey, R. A.; Quach, T. D. Tetrahedron Lett. 2001, 42, 9099. (b) Molander, G. A.; Biolatto, B. Org. Lett. 2002, 4, 1867. (c) Molander, G. A.; Biolatto, B. J. Org. Chem. 2003, 68, 4302. (d) Yuen, A. K. L.; Hutton, C. A. Tetrahedron Lett. 2005, 46, 7899. (e) Gendrineau, T.; Genet, J. -P.; Darses, S. Org. Lett. 2009, 11, 3486.

    (11) (a) Takaya, Y.; Ogasawara, M.; Hayashi, T. Tetrahedron Lett. 1999, 40, 6957. (b) Hayashi, T.; Takahashi, M.; Takaya, Y.; Ogasawara, M. Org. Synth. 2002, 79, 84.
    (12) (a) Yamamoto, Y.; Takizawa, M.; Yu, X.; Miyaura, N. Angew. Chem. Int. Ed. 2008, 47, 928. (b) Yu, X.; Yamamoto, Y.; Miyaura, N. Synlett 2009, 994.
    (13) Yoshida, K.; Ogasawara, M.; Hayashi, T. J. Org. Chem. 2003, 68, 1901.
    (14) Shintani, R.; Tsutsumi, Y.; Nagaosa, M.; Nishimura, T.; Hayashi, T. J. Am. Chem. Soc. 2009, 131, 13588.
    (15) akaya, Y.; Ogasawara, M.; Hayashi, T.; Sakai, M.; Miyaura, N. J. Am. Chem. Soc. 1998, 120, 5579.
    (16) (a) Itooka, R.; Iguchi, Y.; Miyaura, N. J. Org. Chem. 2003, 68, 6000. (b) Sakuma, S.; Miyaura, N. J. Org. Chem. 2001, 66, 8944.
    (17) Lukin, K.; Zhang, Q. Y.; Leanna, M. R. J. Org. Chem. 2009, 74, 929.
    (18) Yamamoto, Y.; Kurihara, K.; Sugishita, N.; Oshita, K.; Piao, D. G.; Miyaura, N. Chem. Lett. 2005, 34, 1224.
    (19) For reviews, see: (a) Bac̈kvall, J. E.; Chinchilla, R.; Nájera, C.; Yus, M. Chem. Rev. 1998, 98, 2291. (b) Nájera, C.; Yus, M. Tetrahedron, 1999, 55, 10547. (c) Prilezhaeva, E. N. Russ. Chem. Rev. 2000, 69, 367. (d) Meadows, D. C.; Gervay-Hague, J. Med. Res. Rev. 2006, 26, 793. (e) Back, T. G. Can. J. Chem. 2009, 87, 1657.
    (20) For selected examples using chiral -amino sulfones in the synthesis (a) (synthesis amino acids) Gaeta, L. S. L.; Czarniecki, M.; Spaltenstein, A. J. Org. Chem. 1989, 54, 4004. (b) (amino acids) Knight, D. W.; Sibley, A. W. Tetrahedron Lett. 1993, 34, 6607. (c)(synthesis amino acids) Rao, A. V. R.; Gurjar, M. K.; Pal, S. Pariza, R. J.; Chorghade, M. S. Tetrahedron Lett. 1995, 36, 2505. (d) (amino acids) Carretero, J. C. Arrayás, R. G. J. Org. Chem. 1998, 63, 2993. (e) (amino acids) Ermolenko, L.; Sasaki, N. A.; Potier, P. J. Chem. Soc., Perkin Trans.1 2000, 2465. (f) (amino acids) Mirilashvili, S.; Chasid-Rubinstein N.; Albeck, A. Eur. J. Org. Chem. 2010, 4671 (g) (Michael addition) Carretero, J. C.; Arrayás, R. G.; Gracia, I. S. Tetrahedron Lett. 1997, 38, 8537. (h) (anion addition) Kumareswarm, R.; Hassner, A. Tetrahedron Lett. 2000, 41, 8157. (i) (anino addition) Kumareswarm, R.; Hassner, A. Tetrahedron: Asymmetry 2001, 12, 2269.
    (21) (a) Zajac, M.; Peters, R. Chem. Eur. J. 2009, 15, 8204. (b) Man, H.-W.; Schafer, P.; Wong, L. M.; Patterson, R. T.; Corral, L. G.; Raymon, H.; Blease, K.; Leisten, J.; Shirley, M. A.; Tang, Y.; Babusis, D. M.; Chen, R.; Stirling, D.; Muller, G. W. J. Med. Chem. 2009, 52, 1522. (c) Wada, C. K.; Holms, J. H.; Curtin, M. L.; Dai, Y.; Florjancic, A. S.; Garland, R. B.; Guo, Y.; Heyman, H. R.; Stacey, J. R.; Steinman, D. H.; Albert, D. H.; Bouska, J. S.; Elmore, I. N.; Goodfellow, C. L.; Marcotte, P. A.; Tapang, P.; Morgan, D. W.; Michaelides, M. R.; Davidsen, S. K. J. Med. Chem. 2002, 45, 219. (d) McIntyre, J. A.; Castaner, J.; Drugs Future 2004, 29, 985.
    (22) (a) Soler, J. G.; Bartolomé, A.; Roselló, M. S. Org. Lett. 2003, 5, 2707. (b) Velázquez, F.; Arasappan, A.; Chen, K.; Sannigrahi, M.; Venkatraman, S.; McPhail, A. T.; Chan, T.-M.; Shih, N.-Y.; Njoroge, F. G. Org. Lett. 2006, 8, 789. (c) Zhang, H.; Li, Y.; Xu, W.; Zheng, W.; Zhou, P.; Sun, Z. Org. Biomol. Chem. 2011, 9, 6502.
    (23) (5) (a) Enders, D.; Müeller, S. F.; Raabe, G. Angew. Chem., Int. Ed. 1999, 38, 195. (b) Enders, D.; Müeller, S. F.; Raabe, G.; Runsink, J. Eur. J. Org. Chem. 2000, 879.
    (24) (a) Ruchelman, A. L.; Connolly, T. J. Tetrahedron: Asymmetry, 2015, 26, 553. (b) Jiang, J.; Wang, Y.; Zhang, X. ACS Catal. 2014, 4, 1570. For related work on asymmetric hydrogenation of -acetylamino vinylsulfides, see: (c) Gao, W. Lv, H,; Zhang, Z. Org. Lett. 2017, 19, 2877.
    (25) For seminal reviews, see: (a) Hayashi, T. Synlett 2001, 879. (b) Fagnou, K.; Lautens, M. Chem. Rev. 2003, 103, 2829. (c) Hayashi, T.; Yamasaki, K. Chem. Rev. 2003, 103, 2829. (d) Edwards, H. J.; Hargrave, J. D.; Penrose, S. D.; Frost, C. G. Chem. Soc. Rev. 2010, 39, 2093. (e) Glorius, F. Angew. Chem., Int. Ed. 2004, 43, 3364. (f) Johnson, J. B.; Rovis, T. Angew. Chem., Int. Ed. 2008, 47, 840. (g) Defieber, C.; Grützmacher, H.; Carreira, E. M. Angew. Chem., Int. Ed. 2008, 47, 4482. (h) Shintani, R.; Hayashi, T. Aldrichimica Acta 2009, 42, 31. (h) Tian, P.; Dong, H.-Q.; Lin, G.-Q. ACS Catal. 2012, 2, 95. (i) Chen, D.; Xu, M.-H. Youji Huaxue 2017, 37, 1589−1612.
    (26) (a)Mauleón, P.; Carretero, J. C. Org. Lett. 2004, 6, 3195. (b) Mauleón, P.; Carretero, J. C. Chem. Commun. 2005, 4961. (c) Mauleón, P.; Alonso, I.; Rivero, M. R.; Carretero, J. C. J. Org. Chem. 2007, 72, 9924.
    (27) Yoshida, K.; Hayashi, T. J. Am. Chem. Soc. 2003, 125, 2872.
    (28) For related arylation of -phthaloyl acrylates, see: Nishimura, T.; Wang, J.; Nagaosa, M.; Okamoto, K.; Shintani, R.; Kwong, F.-Y.; Yu, W.-Y.; Chan, A. S. C.; Hayashi, T. J. Am. Chem. Soc. 2010, 132, 464.
    (29) (a) Nishimura, T.; Takiguchi, Y.; Hayashi, T. J. Am. Chem. Soc. 2012, 134, 9086. (b) Lim, K. M.-H.; Hayashi, T. J. Am. Chem. Soc. 2015, 137, 3201.
    (30) Uozumi, Y.; Sang-Yong, L.; Hayashi, T., Tetrahedron Lett. 1992, 33, 7185-7188.
    (31) Hayashi, T; Tokunaga, N; Otomaru, Y; Ueyama, R; Shintani, R J. Am. Chem. Soc. 2004, 126,13584.
    (32) Defieber, C.; Paquin, J. –F;Serna, S.; Carreira, E. M. Org. Lett. 2004, 6, 3873.
    (33) Lin, G. Q.; Wang, Z. Q.; Feng, C. G.; Xu, M. H. J. Am. Chem. Soc. 2007, 129, 5336.
    (34) U.S. Patent 7,427,638, 2008.
    (35) Euler, V. Naunyn-Schmiedeberg's Arch. Pharmacol. 1934, 175, 78.
    (36) Collins, P. W.; Djuric, S. W. Chem. Rev. 1993, 93, 1533.
    (37) (a) Wang, Y.; Bolos, J.; Serradell, N. ́ Drugs Future 2006, 31, 788. (b) Sorbera, L. A.; Castañer, J. Drugs Future 2000, 25, 41. (c) Sorbera,L. A.; Leeson, P. A.; Rabasseda, X.; Castañer, J. Drugs Future 2001, 26, 433. (d) Watson, P. G. Drugs Today 1999, 35, 449. (e) Lacy, B. E.; Levy, L. C. Clin. Interv. Aging 2008, 3, 357.
    (38) (a) Funk, C. D. Science 2001, 294, 1871. (b) Das, S.; Chandrasekhar, S.; Yadav, J. S.; Gree, R. ́ Chem. Rev. 2007, 107, 3286
    (39)Van Dorp, D. A.; Beerthuis, R. K. ; Nugteren, D. H.; Vonkeman, H. Nature 1964, 203, 839.
    (40) Corey, E. J.; Weinshenker, N. M.; Schaaf, T. K.; Huber, W. J. Am. Chem. Soc. 1969, 91, 5675.
    (41) (a) Stork, G.; Isobe, M. J. Am. Chem. Soc. 1975, 97, 4745. (b) Davis, R.; Untch, K. G. J. Org. Chem. 1979, 44, 3755.
    (42) Suzuki, M.; Kawagishi, T.; Noyori, R. Tetrahedron Letters 1982, 52, 5563
    (43) Suzuki, M.; Yanagisawa, A.; Noyori, R. J. Am. Chem. Soc. 1985, 107, 3348.
    (44) (a) Sih, C. J.; Price, P.; Sood, R.; Salomon, R. G.; Peruzzotti, G.; Casey, M. J. Am. Chem. Soc. 1972, 94, 3643. (b) Kluge, A. F.; Untch, K. G.; Fried, J. H. J. Am. Chem. Soc. 1972, 94, 7827. (c) Pappo, R.; Collins, P. W. Tetrahedron Lett. 1972, 13, 2627.
    (45) (a) Henschke, J. P.; Liu, Y. L.; Chen, Y. F.; Meng, D. C.; Sun, T. U.S. Patent 7,897,795, 2011. (b) Henschke, J. P.; Liu, Y. L.; Xia, L. Z.; Chen, Y. F. U.S. Patent 8,846,958, 2014. (c) Henschke, J. P.; Liu, Y. L.; Huang, X. H.; Chen, Y. F.; Meng, D. C.; Xia, L. Z.; Wei, X. Q.; Li, D. H.; Huang, Q. A.; Sun, T.; Wang, J.; Gu, X. B.; Huang, X. Y.; Wang, L. H.; Xiao, J.; Qiu, S. H. Org. Process Res. Dev. 2012, 16, 1905.
    (46) Behling, J. R.; Babiak, K. A.; Ng, J. S.; Campbell, A. L.; Moretti, R.; Koerner, M.; Lipshutz, B. H. J. Am. Chem. Soc. 1988, 110, 2641.
    (47) Wen, W. H. U.S. Patent Appl. 2014/0046086 A1, 2014.
    (48) de la Herran, G.; ́Mba, M.; Murcia, M. C.; Plumet, J.; Csaky ́, A. G. Org. Lett. 2005, 7, 1669.
    (49) 廖柏翔(2014)。碩士論文,國立臺灣師範大學化學研究所,臺北,臺灣。
    (50) (a) Tucker, C. E.; Davidson, J.; Knochel, P. J. Org. Chem. 1992, 57, 3482. (b) Clay, J. M.; Vedejs, E. J. Am. Chem. Soc. 2005, 127, 5766. (c) Kalinin, A. V.; Scherer, S.; Snieckus, V. Angew. Chem., Int. Ed. 2003, 42, 3399. (d) Josyula, K. V. B.; Gao, P.; Hewitt, C. Tetrahedron Lett. 2003, 44, 7789.
    (51) (a) Henderson, R. K.; Jimenez-Gonza ́ lez, C.; Constable, D. J. ́C.; Alston, S. R.; Inglis, G. G. A.; Fisher, G.; Sherwood, J.; Binks, S. P.; Curzons, A. D. Green Chem. 2011, 13, 854. (b) Laird, T. Org. Process Res. Dev. 2012, 16, 1. (c) Prat, D.; Pardigon, O.; Flemming, H.-W.; Letestu, S.; Ducandas, V.; Isnard, P.; Guntrum, E.; Senac, T.; Ruisseau, S.; Cruciani, P.; Hosek, P. Org. Process Res. Dev. 2013, 17, 1517.
    (52) For reviews, see: (a) Practical Microwave Synthesis for Organic Chemists; Kappe, C. O.; Dallinger, D.; Murphree, S. S., Eds.; WileyVCH: Weinheim, 2009. (b) Microwave Assisted Organic Synthesis; Tierney, J.; Lidstro ̈m, P.; Eds.; Blackwell Publishing: Oxford, 2007. (c) Microwave-Assisted Synthesis of Heterocycles; van der Eycken, E.; Kappe, C. O.; Eds.; Springer: Berlin, 2006.
    (53) (a) Kina, A.; Iwamura, H.; Hayashi, T. J. Am. Chem. Soc. 2006, 128, 3904. (b) Kina, A.; Yasuhara, Y.; Nishimura, T.; Iwamura, H.; Hayashi, T. Chem. Asian J. 2006, 1, 707.
    (54) Rodríguez, A.; Nomen, M.; Spur, B. W.; Godfroid, J. J. Eur. J. Org. Chem. 1999, 10, 2655.
    (55) C. Lima, C. F. R. A.; Rodrigues, A. S. M. C.; Silva, V. L. M.; Silva, A. M. S.; Santos, L. M. N. B. F. ChemCatChem 2014, 6, 1291.
    (56) Toro, A.; Nowak, P.; Deslongchamps, P. ́ J. Am. Chem. Soc. 2000, 122, 4526.
    (57) Ho, H.-E.; Asao, N.; Yamamoto, Y.; Jin, T. Org. Lett. 2014, 16, 4670.
    (58) Movassaghi, M.; Hunt, D. K.; Tjandra, M. J. Am. Chem. Soc. 2006, 128, 8126.
    (59) Gooding, O. W.; Beard, C. C.; Cooper, G. F.; Jackson, D. Y. J. Org. Chem. 1993, 58, 3681.
    (60) L’Heureux, A.; Beaulieu, F.; Bennett, C.; Bill, D. R.; Clayton, S.; LaFlamme, F.; Mirmehrabi, M.; Tadayon, S.; Tovell, D.; Couturier, M. J. Org. Chem. 2010, 75, 3401.
    (61) Kalinin, A. V.; Scherer, S.; Snieckus, V. Angew. Chem., Int. Ed. 2003, 42, 3399.
    (62) Lennox, A. J. J.; Lloyd-Jones, G. C. Angew. Chem., Int. Ed. 2012, 51, 9385.

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