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研究生: 巴朗
Barange Deepak Kumar
論文名稱: 硝基烯與環狀1,3-雙羰基化合物在水的條件下進行反應之探討以及內環磺胺類衍生物之合成
Reactions of nitroalkenes with cyclic 1,3-dicarbonyl compounds under ‘on water’ condition and novel synthesis of fused Sultam derivatives
指導教授: 姚清發
Yao, Ching-Fa
學位類別: 博士
Doctor
系所名稱: 化學系
Department of Chemistry
論文出版年: 2012
畢業學年度: 100
語文別: 英文
論文頁數: 393
中文關鍵詞: 在水的條件1,3-雙羰基化合物硝基苯乙烯[3+2]環加成反應Suzuki偶聯反應Heck 偶聯反應Sonogashira偶聯反應
英文關鍵詞: "On water", 1,3-dicarbonyl compounds, nitrostyrenes, [3+2]cycloaddition, Suzuki coupling, Heck coupling, Sonogashira coupling
論文種類: 學術論文
相關次數: 點閱:143下載:2
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  • 本論文主要分為三個章節。在第一章節,主要是分為四個部分,其中A部分是回顧有關於在水的條件下所進行反應之相關文獻報導,在B部分和C部分是描述硝基苯乙烯與環狀1,3-雙羰基化合物在水的條件下進行反應以及內環磺胺類衍生物之合成,C部分則是介紹藉由矽膠在微波條件下進行一鍋化兩步合成以羥基亞胺基二氫苯呋喃類之衍生物。

    在第二章節中,介紹藉由過渡金屬催化合成內環磺胺類衍生物以及其多方面的合成應用。在第二章節裡,主要是分為四個部分,其中A部分是回顧有關於合成內環磺胺類衍生物之相關文獻報導,這部分同時也簡要概述有關於三氮唑以往的合成方式和文獻探討。B部分是描述有效率且以一鍋化的方式,藉由銅催化[3+2]環加成反應來合成triazolothiadiazepine-1,1-dioxide之衍生物,以及利用上述的方法合成分別以吲哚啉和噻吩結合內環磺胺類之衍生物。而C部分是介紹一種新穎的合成策略,其藉由溴環化反應來合成出含有雙溴的呋喃結合內環磺胺類之衍生物,而此合成方法也可以應用於合成tetrahydrofuroisoquinolin-5(9bH)-one之衍生物。D部分是探討一種有效率且具有位向選擇性的合成方法,其藉由碘環化反應來合成出4-iodo-2,3-disubstituted-2H-thieno[3,2-e][1,2]thiazine-1,1-dioxide之衍生物。將所得到的產物4-iodo-2,3-disubstituted-2H-thieno [3,2-e] [1,2] thiazine-1,1-dioxide與一系列的硼酸(Suzuki偶聯反應)和活潑烯烴(Heck 偶聯反應)進行偶聯反應。經Sonogashira偶聯反應後的產物可以有效率地合成為疊氮化合物的前驅物,其可以多方面的合成應用於合成出三氮唑結合噻吩和內環磺胺類之衍生物。在第三章節中,主要是收錄整本論文中所有標記的化合物之1H和13C光譜圖以及X光晶體的數據。

    The content of this dissertation is divided into three parts. The part I is subdivided into four sections. Section A, illustrate the overview on ‘on water’ reactions and
    related literature review. Section B and C describes the ‘on water’ reactions of nitrosytrenes with cyclic 1,3-dicarbonyl compounds and also the synthesis of
    hydroxyiminodihydrofuroquinolinone derivatives. Section D deals with one-pot, twostep synthesis of hydroxyiminodihydrobenzofurans mediated by silica gel under
    microwave activation condition.
    Part II deals with the synthesis of fused sultam derivatives by using transition metal catalysed reactions and their appliation towards diversity oriented synthesis. Part II is subdivided into four sections. Section A, deals with overview, classification and synthetic approaches of fused Sultam derivatives. This section also describe the brief overview on triazole synthesis and literature survey. Section B, describes an efficient and one-pot synthesis of triazolothiadiazepine-1,1-dioxide derivatives via copper
    catalyzed tandem [3+2] cycloaddition/N-Arylation and utilization of this method to synthesize indoline and thiophene fused sultam. Section C deals with the novel
    synthesis of angular diborminated furosultam derivaitves via bromocyclization strategy. This method is also applicable for the synthesis of tetrahydrofuroisoquinolin-
    5(9bH)-one. Section D, demonstrate an efficient and regioselective synthesis of 4-iodo-2,3-disubstituted-2H-thieno[3,2-e][1,2]thiazine-1,1-dioxide derivatives via
    iodocyclization approach. The resulting 4-iodo-2,3-disubstituted-2H-thieno[3,2-e][1,2]thiazine-1,1-dioxide utilized to couple with a array of boronic acids (Suzuki
    coupling) and activated alkenes (Heck coupling). The Sonogashira coupled product was efficiently transformed to azido precursor, which was exploited for the diversity
    oriented synthesis of triazole linked thieno-sultam derivatives.
    Part III comprises of 1H and 13C NMR spectral copies and X-Ray crystallograpic data of all the compounds incorporated in this thesis.

    Abbreviations i-iv Abstract v-xiv Part I Part I, Section-A: Overview on “on water” reactions and Michael addition I.A.1 Introduction 1 I.A.2 “On water” approaches 2 I.A.3 Michael addition in the presence of water 16 I.A.4 “On water” Michael addition 17 I.A.5 References 18 Part I, Section-B: Facile and highly efficient method for the C-alkylation of 2-hydroxy-1,4-naphthoquinones to nitroalkenes under catalyst free ‘on water’ conditions I.B.1 Introduction 23 I.B.2 Review of literature 24 I.B.3 Results and discussions 27 I.B.4 Conclusion 32 I.B.5 Experimental Section 32 I.B.6 References 37 Part I, Section-C: Synthesis of C3-nitroalkylated-4-hydroxycoumarin and hydroxyiminodihydrofuroquinolinone derivatives via Michael addition of cyclic 1,3-dicarbonyl compounds to -nitrostyrenes I.C.1 Introduction 40 I.C.2 Review of literature 42 I.C.3 Results and discussions 42 I.C.4 Conclusion 52 I.C.5 Experimental Section 52 I.C.6 References 61 Part I, Section-D: A mild and convenient one-pot, two-step synthesis of hydroxyiminodihydrobenzofurans mediated by silica gel under microwave activation conditions I.D.1 Introduction 65 I.D.2 Review of literature 65 I.D.3 Results and discussions 67 I.D.4 Conclusion 72 I.D.5 Experimental Section 73 I.D.6 References 82 Part II Part-II, Section-A: Overview on cyclic sulfonamides (Sultam) and triazoles II.A.1 Introduction 85 II.A.2 Synthetic approaches to sultam 87 II.A.3 Overview on synthesis of triazoles 97 II.A.4 References 100 Part-II, Section-B: One-pot Synthesis of Triazolothiadiazepine-1,1-dioxide Derivatives via Copper Catalyzed Tandem [3+2] Cycloaddition/N-Arylation II.B.1 Introduction 103 II.B.2 Review of literature 103 II.B.3 Results and discussions 105 II.B.4 Conclusion 112 II.B.5 Experimental Section 113 II.B.6 References 126 Part-II, Section-C: Synthesis of Angular Dibrominated Furosultam Scaffolds via NBS mediated Bromocyclization Strategy II.C.1 Introduction 129 II.C.2 Review of literature 129 II.C.3 Results and discussions 130 II.C.4 Conclusion 143 II.C.5 Experimental Section 144 II.C.6 References 167 Part-II, Section-D: Regioselective synthesis of 4-iodo-2,3,-disubstituted thiophene fused sultam derivatives via iodocyclization strategy and its application towards triazole linker II.D.1 Introduction 169 II.D.2 Review of literature 170 II.D.3 Results and Discussions 170 II.D.4 Conclusion 178 II.D.5 Experimental Section 179 II.C.6 References 189 Part-III III.A.1 X-Ray Crystallographic data 189 III.B.1 1H and 13C NMR Spectral copies 206 List of publications 393

    1. (a) Lindström U. M. Organic reactions in water: Principles, Strategies and Applications Blackwell publishers, New York, 2007; (b) Polshettiwar, V.; Varma, R. S. Acc. Chem. Res. 2008, 41, 629.
    2. (a) Breslow, R. Acc. Chem. Res. 1991, 24, 159. (b) Li, C. J.; Chang, T. H. Organic Reactions in Aqueous Media, Wiley, New York, 1997; 7950; (c) Lindström, U. M. Chem. Rev. 2002, 102, 275; (d) Shu, K.; Kei, M. Acc. Chem. Res. 2002, 35, 209; (e) Li, C.-J.; Chem. Rev. 2005, 105, 3095; (f) Pirrung, M. C. Chem. Eur. J. 2006, 12, 1312.
    3. (a) Narayan, S.; Muldoon, J. Finn, M. G.; Fokin, V. V.; Kolb, H. C.; Sharpless, K.B. Angew. Chem. Int. Ed. 2005, 44, 3275; (b) Klijin, J. E.; Engberts, J. B. F. N. Nature 2005, 435, 746; (c) Zhang, H. B.; Liu, L.; Chen, Y. J.; Wang, D.; Li, C. -J. Eur. J. Org. Chem. 2006, 869; (d) Price, B. K.; Tour, J. J. Am. Chem. Soc. 2006, 128, 12899; (e) Gonzalez-Cruz, D.; Tejedor, D.; deArmas, P.; Morales, E. Q.; Garcia-Tellado, F. Chem. Commun. 2006, 2798; (f) Gonzsles-Cruz, D.; Tejedor, D.; de Armas, P.; GarcPa-Telaldo, F. Chem. Eur. J. 2007, 13, 4823; (g) Chakraborti, A. K.; Rudrawar, S.; Jadhav, K. B.; Kaur, G.; Chaneshwara, S. V. Green Chem. 2007, 1335; (h) El-Batta, A.; Jiang, C.; Zhao, W.; Anness, R.; Cooksy, A. L.; Bergdahl, M.; J. Org .Chem. 2007, 72, 5244; (i) Huang, J.; Zhang, X.; Armstrong, D. W. Angew. Chem. Int. Ed. 2007, 46, 9073; (j) Guizzetti, S.; Benaglia, M.; Raimondi, L.; Celentano, G. Org. Lett. 2007, 9, 1247; (k) Turner, G. L.; Morris, J. A.; Greaney, M. F. Angew. Chem. Int. Ed. 2007, 46, 7996; (l) Shapiro, N.; Vigalok, A. Angew. Chem. Int. Ed. 2008, 47, 2849; (m) Cozzi, P. G.; Zoli, L. Angew. Chem. Int. Ed. 2008, 47, 4162; (n) Santi, C.; Santoro, S.; Battistelli, B.; Testaferri, L.; Tiecco, M. Eur. J. Org. Chem. 2008, 5387; (o) Wang, F.; Fu, H.; Jiang, Y.; Zhao, Y. Adv. Synth. Catal. 2008, 350, 1830; (p) Zhang, Q. -Y.; Liu, B. -K.; Chen, W.-Q.; Wu, Q.; Lin X.-F. Green Chem. 2008, 972; (q) Pirrung, M. C.; Sarma, K. D.; Wang, J. J. Org. Chem. 2008, 73, 8730.
    4. (a) Jeffrey, G.A. An Introduction of Hydrogen Bonding, Oxford University Press, Oxford 1997. (b) Pimentel, G. C.; McLellan, A. L. The Hydrogen Bond, Freeman, San Francisco, 1960; (c) McCauley , J. A.; Navasota , K.; Lander, P. A.; Mischke, S. G.; Semones, M. A. ; Kishi, Y. J. Am. Chem. Soc., 1998, 120 , 7647; (d) Noda, T.; Ishiwata, A.; Uemura, S.; Sakamoto, S.; Hirama, M. Synlett 1998, 298; (e) Noda, T.; Ishiwata, A.; Uemura, S.; Sakamoto, S;. Hirama, M. Synlett 1998 , 298; (f) Satake, M. ; Ofuji, K.; Naoki, H.; James, K. J.; Furey, A.; McMahon, T.; Silke, J.; Yasumoto, T. J. Am. Chem.Soc. 1998, 120 , 9967; (g) Nicolaou, K. C.; Pihko, P. M.; Bernal, F. ; Frederick, M. O.; Qian , W.; Uesaka, N.; Diedrichs, N.; Hinrichs, J.; Koftis, T. V.; Loizidou, E.; Petrovic, G.; Rodriquez, M.; Sarlah, D.; Zou, N. J. Am. Chem. Soc. 2006, 128, 2244. (h) Rigby, J. H.; Maharoof, U. S. M.; Mateo, M. E. J. Am. Chem. Soc. 2000, 122, 6624.
    5. (a) Asami, Y.; Kakeya, H.; Onose, R.; Yoshida, A.; Matsuzaki, H.; Osada, H. Org. Lett. 2002, 4, 2845. (b) Allen, J.G.; Danishefsky, S. J. J. Am. Chem. Soc. 2001, 123, 351. (c) White, J. D.; Somers, T. C. J. Am. Chem. Soc., 1994, 116, 9912. (d) Fettes, A.; Carreira, E. M. J. Org. Chem. 2003, 68, 9274. (e) Cook, J. L.; Hunter , C.A.; Low , C. M. R.; Perez-Velasco, A.; Vinter, J. G. Angew. Chem. Int. Ed. 2007, 46, 3706 and references cited therein.
    6. Hayashi, Y. Angew. Chem. Int. Ed. 2006, 45, 8103.
    7. (a) P. A. Grieco, P. Garner, Z. He, Tetrahedron Lett. 1983, 24, 1897. ; (b) P. A. Grieco, K. Yoshida, P. Garner, J. Org. Chem. 1983, 48, 3137
    8. Rideout, D. C.; Breslow, R. J. Am. Chem. Soc. 1980, 102, 7816.
    9. Rideout, D. C.; Moitra, U.; Breslow, R. Tetrahedron Lett. 1983, 24, 1901.
    10. Blokzijl, W.; Engberts, J. B. F. N. Angew. Chem., Int. Ed. 1993, 32, 1545.
    11. Breslow, R. In Structure and Reactivity in Aqueous Solution; Cramer, C. J., Truhlar, D. G., Eds.; American Chemical Society: Washington, DC, 1994; Vol. 568, pp 291-302.
    12. Rieber, N., Alberts, J., Lipsky, J. A., Lemal, D. M. J. Am. Chem.Soc. 1969, 91, 5668.
    13. Platz, R.; Fuchs, W.; Rieber, N.; Samuel, U.-R.; Jung, J. DE Patent 2615878, 1977.
    14. Platz, R.; Fuchs, W.; Rieber, N.; Jung, J. DE Patent 2742034, 1979.
    15. Y. Leblanc, R. Zamboni, M. A. Bernstein, J. Org. Chem. 1991, 56, 1971.
    16. Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Angew. Chem., Int. Ed. 2001, 40, 2004.
    17. Li, Z.; Seo, T. S.; Ju, J. Tetrahedron Lett. 2004, 45, 3143.
    18. Butler, R. N.; Coyne, A. G.; Moloney, E. M. Tetrahedron Lett. 2007, 48, 3501.
    19. Butler, R. N.; Coyne, A. G.; Cunningham, W. J.; Moloney, E. M.; Burke, L. A. HelV. Chim. Acta 2005, 88, 1611.
    20. Gonzalez-Cruz, D.; Tejedor, D.; de Armas, P.; Morales, E. Q.; Garcia-Tellado, F. Chem. Commun. 2006, 2798.
    21. Gonzalez-Cruz, D.; Tejedor, D.; de Armas, P.; Garcia-Tellado, F.Chem. Eur. J. 2007, 13, 4823.
    22. Bala, K.; Hailes, H. C. Synthesis 2005, 3423.
    23. Gajewski, J. J.; Jurayj, J.; Kimbrough, D. R.; Gande, M. E.; Ganem, B.; Carpenter, B. K. J. Am. Chem. Soc. 1987, 109, 1170.
    24. Brandes, E.; Grieco, P. A.; Gajewski, J. J. J. Org. Chem. 1989, 54, 515.
    25. Demko, Z. P.; Sharpless, K. B. J. Org. Chem. 2001, 66, 7945.
    26. Hulme, C. Multicompon. React. 2005, 311.
    27. Domling, A. Curr. Opin. Chem. Biol. 2002, 6, 306.
    28. Ugi, I.; Werner, B. Methods Reagents Green Chem. 2007, 3.
    29. Das Sarma, K.; Pirrung, M. C. J. Am. Chem. Soc. 2004, 126, 444.
    30. Pirrung, M. C.; Das Sarma, K. Tetrahedron 2005, 61, 11456.
    31. Azizi, N.; Saidi, M. R. Org. Lett. 2005, 7, 3649.
    32. Saidi, M. R.; Ziyaei-Halimjani, A. Can. J. Chem. 2006, 84, 1515.
    33. Vilotijevic, I.; Jamison, T. F. Science 2007, 317, 1189.
    34. Converso, A.; Burow, K.; Marzinzik, A.; Sharpless, K. B.; Finn, M. G. J. Org. Chem. 2001, 66, 4386.
    35. Converso, A.; Saaidi, P. L.; Sharpless, K. B.; Finn, M. G. J. Org.Chem. 2004, 69, 7336.
    36. Cozzi, P. G.; Zoli, L. Green Chem. 2007, 9, 1292.
    37. Cozzi, P. G.; Zoli, L. Angew. Chem., Int. Ed. 2008, 47, 4162.
    38. Tandon, V.; Maurya, H. Tetrahedron Lett. 2009, 50, 5896.
    39. Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem. Int.Ed. 2002, 41, 2596.
    40. Tornøe, C. W.; Christensen, C.; Meldal, M. J. Org. Chem. 2002, 67, 3057.
    41. Wei, C.; Li, Z.; Li, C.-J. Synlett 2004, 1472.
    42. Wei, C. M.; Li, C. J. J. Am. Chem. Soc. 2002, 124, 5638.
    43. Chen, L.; Li, C. J. Chem. Commun. 2004, 2362.
    44. Bhattacharya, S.; Sengupta, S. Tetrahedron Lett. 2004, 45, 8733.
    45. Churruca, F.; SanMartin, R.; Tellitu, I.; Domı´nguez, E. Synlett 2005, 3116.
    46. Ine´s, B.; Moreno, I.; SanMartin, R.; Domı´nguez, E. J. Org. Chem.2008, 73, 8448.
    47. Ine´s, B.; SanMartin, R.; Churruca, F. t.; Domı´nguez, E.; Urtiaga, M. K.; Arriortua, M. a. I. Organometallics 2008, 27, 2833.
    48. Anderson, K. W.; Buchwald, S. L. Angew. Chem., Int. Ed. 2005, 44, 6173.
    49. Guss, C. O.; Rosenthal, R. J. Am. Chem. Soc. 1955, 77, 2549.
    50. Podgorsek, A.; Stavber, S.; Zupan, M.; Iskra, J. Green Chem. 2007, 9, 1212.
    51. Pravst, I.; Zupan, M.; Stavber, S. Tetrahedron Lett. 2006, 47, 4707.
    52. Oshovsky, G.G; Reinhoudt, D.N.; Verboom, W. Angew Chem. Int. Ed. 2007, 46, 2366.
    53. (a) List, B. Chem. Rev. 2007, 107, 5413. (b) Dalko, P. I.; Moisan L. Angew. Chem. Int. Ed. 2004, 43, 5138. (c) Enders, D.; Christoph, G.; Hüttl, M. R. M. Angew. Chem. Int. Ed. 2007, 46, 1570. (d) Halland N.; Hansen, T.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2003, 42, 4955
    54. Zu, L.; Wang, J.; Wang, W. Org. Lett. 2006, 8, 3077.
    55. Zhu, S.; Yu, S.; Ma, D. Angew. Chem. Int. Ed. 2008, 47, 545.
    56. (a) R. Ling, U.V.Ekhato, J.R.Rubin, D. J. Wustrow, Tetrahedron 2001, 57, 6579 (b) R. Galeazzi, G. Martelli, G. Mobbili, M. Orena, S. Rinaldi, Tetrahedron : Asymmetry 2003, 14, 3353.
    57. (a)Barange, D. K.; Raju, B, R.; Kavala, V.; Kuo, C.-W.; Tu, Y.-C.; Yao, C.-F. Tetrahedron 2010, 66, 3754–3760. (b) Barange, D, K.; Kavala, V.; Kuo, C.-W.; Tseng, C.; Tu, Y.-C.; Yao, C.-F. Tetrahedron Lett. 2009, 50, 5116. (c) Habib, P. M.; Kavala, V.; Raju, B. R.; Kuo, C-W.; Huang, W C.; Yao, C.-F. Eur. J. Org. Chem. 2009, 4503.

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