User menu

Copper-Catalysed Domino Silylative Aldol Reaction Leading to Stereocontrolled Chiral Quaternary Carbons.

Bibliographic reference Welle, Alexandre ; Petrignet, Julien ; Tinant, Bernard ; Wouters, Johan ; Riant, Olivier. Copper-Catalysed Domino Silylative Aldol Reaction Leading to Stereocontrolled Chiral Quaternary Carbons.. In: Chemistry (Weinheim an der Bergstrasse, Germany), Vol. 16, no. 36, p. 10980-3 (2010)
Permanent URL http://hdl.handle.net/2078.1/33148
  1. Tietze, Chem. Rev., 96, 115 (1996)
  2. Fogg, Coord. Chem. Rev., 248, 2365 (2004)
  3. Chapman, Synlett, 1 (2007)
  4. Nishiyama, Top. Curr. Chem., 279, 105 (2007)
  5. Han, Synlett, 2669 (2008)
  6. Shiomi, Org. Lett., 11, 1011 (2009)
  7. Ohmiya, Tetrahedron Lett., 49, 2388 (2008)
  8. Joensuu, J. Am. Chem. Soc., 130, 7328 (2008)
  9. Lumby, Org. Lett., 9, 4367 (2007)
  10. Lumby, Tetrahedron, 64, 7729 (2008)
  11. Angew. Chem. Int. Ed., 46, 498 (2007)
  12. Rendler, Angew. Chem., 119, 504 (2007)
  13. Deutsch, Chem. Rev., 108, 2916 (2008)
  14. Shibasaki, Chem. Rev., 108, 2853 (2008)
  15. Riant, Copper(I) Hydride Reagents and Catalysts in The Chemistry of Organocopper Compounds, 731 (2009)
  16. Ooi, Tetrahedron Lett., 40, 2133 (1999)
  17. Chiu, Tetrahedron Lett., 39, 9229 (1998)
  18. Chiu, Tetrahedron Lett., 39, 9229 (1998)
  19. Chiu, Org. Lett., 3, 1901 (2001)
  20. Chiu, Tetrahedron Lett., 42, 4091 (2001)
  21. Chiu, Chem. Commun., 2308 (2004)
  22. Chung, Synlett, 55 (2005)
  23. Agapiou, J. Am. Chem. Soc., 126, 4528 (2004)
  24. Lam, Org. Lett., 7, 4225 (2005)
  25. Lam, Org. Lett., 7, 5743 (2005)
  26. Lipshutz, J. Am. Chem. Soc., 130, 14378 (2008)
  27. Deschamp, Org. Lett., 11, 1217 (2009)
  28. Oswald, Org. Lett., 11, 4504 (2009)
  29. Welle, Org. Lett., 8, 6059 (2006)
  30. Angew. Chem. Int. Ed., 45, 1292 (2006)
  31. Deschamp, Angew. Chem., 118, 1314 (2006)
  32. Zhao, Tetrahedron Lett., 47, 1403 (2006)
  33. Zhao, J. Am. Chem. Soc., 128, 14440 (2006)
  34. Oisaki, J. Am. Chem. Soc., 128, 7164 (2006)
  35. Chuzel, Org. Lett., 8, 5943 (2006)
  36. Du, J. Am. Chem. Soc., 130, 16146 (2008)
  37. Chen, J. Am. Chem. Soc., 131, 11664 (2009)
  38. Kato, Synlett, 1299 (2009)
  39. Ohmura, Bull. Chem. Soc. Jpn., 82, 29 (2009)
  40. Burks, Chem. Commun., 4717 (2007)
  41. Angew. Chem. Int. Ed., 45, 5675 (2006)
  42. Walter, Angew. Chem., 118, 5803 (2006)
  43. Ohmiya, Org. Lett., 11, 5618 (2009)
  44. Ohmura, J. Am. Chem. Soc., 131, 16624 (2009)
  45. Ohmura, Org. Lett., 11, 2880 (2009)
  46. Walter, Tetrahedron, 65, 5513 (2009)
  47. Ito, J. Am. Chem. Soc., 120, 11196 (1998)
  48. Clark, J. Am. Chem. Soc., 126, 84 (2004)
  49. Lipshutz, J. Am. Chem. Soc., 120, 4021 (1998)
  50. Oestreich, Synlett, 2139 (2004)
  51. Auer, Synthesis, 2113 (2006)
  52. Weickgenannt, Chem. Eur. J., 16, 402 (2010)
  53. Lee, J. Am. Chem. Soc., 132, 2898 (2010)
  54. Gulliver, Inorg. Chim. Acta, 52, 153 (1981)
  55. Suginome, Organometallics, 19, 4647 (2000)
  56. Angew. Chem. Int. Ed., 37, 388 (1998)
  57. Corey, Angew. Chem., 110, 402 (1998)
  58. Denissova, Tetrahedron, 59, 10105 (2003)
  59. Christoffers, Adv. Synth. Catal., 347, 1473 (2005)
  60. Trost, Synthesis, 369 (2006)
  61. Ando, Tetrahedron Lett., 34, 1507 (1993)
  62. Angew. Chem. Int. Ed., 43, 2420 (2004)
  63. Mase, Angew. Chem., 116, 2474 (2004)
  64. Kobayashi, Org. Lett., 7, 4729 (2005)
  65. Wang, Tetrahedron Lett., 46, 5077 (2005)
  66. Denmark, J. Am. Chem. Soc., 129, 14864 (2007)
  67. Ichibakase, Tetrahedron Lett., 49, 4427 (2008)
  68. Zhao, Tetrahedron Lett., 50, 3458 (2009)
  69. Yoshino, J. Am. Chem. Soc., 131, 17082 (2009)
  70. Yamago, J. Org. Chem., 56, 2098 (1991)
  71. Das Jaya Prakash, Chechik Helena, Marek Ilan, A unique approach to aldol products for the creation of all-carbon quaternary stereocentres, 10.1038/nchem.131
  72. Burke, Org. Lett., 6, 405 (2004)
  73. Evans, Top. Stereochem., 13, 1 (1982)
  74. Tietze, Org. Lett., 11, 5230 (2009)