有机化学中的多米诺反应

罗佗平

引用本文: 罗佗平. 有机化学中的多米诺反应[J]. 大学化学, 2004, 19(4): 53-58. doi: 10.3969/j.issn.1000-8438.2004.04.015 shu

有机化学中的多米诺反应

    通讯作者: 罗佗平,
摘要: 寻求在环境友好介质中的“理想的”合成方法,从而实现在温和条件下快速、高选择性的合成,是有机化学发展中的重要目标。在这样的条件下,高效、高选择性、高原子经济性多米诺反应就突显其重要性。本文举例介绍了几种常见的多米诺反应,分析了一些多米诺反应的设计精妙之处.

English

    1. [1] Sadler I H,Simpson T J. Magn Reson Chem, 1992,30:518[1] Sadler I H,Simpson T J. Magn Reson Chem, 1992,30:518

    2. [2] Simpson T J. J Chem Soc Perkin Trans 1,1994:3055[2] Simpson T J. J Chem Soc Perkin Trans 1,1994:3055

    3. [3] Edward M, Croteau D R. Cyclization Enzymes in the Biosynthesis of Monoterpenes, Sesquiterpenes, and Diterpenes,Biosynthesis,Topics in Current Chemistry. Berlin Heidelberg:Springer-Verlag, 1998[3] Edward M, Croteau D R. Cyclization Enzymes in the Biosynthesis of Monoterpenes, Sesquiterpenes, and Diterpenes,Biosynthesis,Topics in Current Chemistry. Berlin Heidelberg:Springer-Verlag, 1998

    4. [4] Abe I,Prestwich G D. J Biol Chem,1994,269:802[4] Abe I,Prestwich G D. J Biol Chem,1994,269:802

    5. [5] Corey E J,Cheng H,Baker C H,et al. JAm Chem Soc,1997,119:1289[5] Corey E J,Cheng H,Baker C H,et al. JAm Chem Soc,1997,119:1289

    6. [6] Feil C,Sussmuth R,Jung G,et al. Eur J Bioch,1996,242:51[6] Feil C,Sussmuth R,Jung G,et al. Eur J Bioch,1996,242:51

    7. [7] Paterson I,Tillyer R D,Smaill J B. Tetrahedron Lett,1993,34:7137[7] Paterson I,Tillyer R D,Smaill J B. Tetrahedron Lett,1993,34:7137

    8. [8] Johnson W S. Angew Chem, 1976,88:33[8] Johnson W S. Angew Chem, 1976,88:33

    9. [9] Hickmott P W, Suschitzky H, Urbani R. J Chem Soc Perkin Trans, 1973(1):2063[9] Hickmott P W, Suschitzky H, Urbani R. J Chem Soc Perkin Trans, 1973(1):2063

    10. [10] Gary H. Posner Chem Rev,1986,86:831[10] Gary H. Posner Chem Rev,1986,86:831

    11. [11] Wuckelt J,Doring M,Langer P,et al. Synlett,1999,468[11] Wuckelt J,Doring M,Langer P,et al. Synlett,1999,468

    12. [12] Begley M J,Pattenden G,Smithies A J,et al. Tetrahedron Lett,1994,35:2417[12] Begley M J,Pattenden G,Smithies A J,et al. Tetrahedron Lett,1994,35:2417

    13. [13] Trost B M,Shi Y. JAm Chem Soc,1992,114:791[13] Trost B M,Shi Y. JAm Chem Soc,1992,114:791

    14. [14] Trost B M,Shi Y. J Am Chem Soc,1993,115:12491[14] Trost B M,Shi Y. J Am Chem Soc,1993,115:12491

    15. [15] Trost B M. Angew Chem Int Ed Engl, 1995,34:259[15] Trost B M. Angew Chem Int Ed Engl, 1995,34:259

    16. [16] Trost B M,Shi Y. J Am Chem Soc,1993,115:9421[16] Trost B M,Shi Y. J Am Chem Soc,1993,115:9421

    17. [17] Negishi E I,Sugihara T,Coperet C,et al. J Am Chem Soc,1994,116:7923[17] Negishi E I,Sugihara T,Coperet C,et al. J Am Chem Soc,1994,116:7923

    18. [18] Tietze L F,Beifuss U,Lokos M,et al. Angew Chem,1990,102:545[18] Tietze L F,Beifuss U,Lokos M,et al. Angew Chem,1990,102:545

    19. [19] Tietze L F,Beifuss U,Lokos M,et al. Angew Chem,Int Ed Engl,1990,29:527[19] Tietze L F,Beifuss U,Lokos M,et al. Angew Chem,Int Ed Engl,1990,29:527

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