Bulletin of the Korean Chemical Society

  • 제22권5호
  • /
  • Pages.443-444
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  • 2001
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Facile Synthesis of Optically Active Styrene Oxide Derivatives by Asymmetric Reduction of Substituted 2-Sulfonyloxyacetophenones with (-)-B-Chlorodiisopinocampheylborane $(^dIpc_2BCI)$

  • 발행 : 20010500
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참고문헌

  1. J. Chem. Soc. Perkin Trans. v.1 Coote, S. J.;Davies, S. G.;Middlemiss, D.;Naylor, A.
  2. Chemistry and Industry Britten, A. Z.
  3. Tetrahedron Lett. v.38 Hett, R.;Fang, Q. K.;Gao, Y.;Hong, Y.;Butler, H. T.;Nie, X.;Wald, S. A.
  4. Bioorg. Med. Chem. Lett. v.4 Badone, D.;Guzzi, U.
  5. Bioorg. Med. Chem. Lett. v.5 Di Phabio, R.;Pietra, C.;Thomas, R. J.;Ziviani, L.
  6. J. Org. chem. v.60 Solladie-Cavallo, A.;Diep-Vohuule, A.
  7. Tetrahedron: Asymmetry v.2 Nieduzak, T. R.;Margolin, A. L.
  8. Tetrahedron v.53 Pedragossa-Moreau, S.;Morisseau, C.;Baratti, J.;Zylber, J.;Archelas, A.;Furstoss, R.
  9. See, ref. 1f.
  10. Tetrahedron Lett. v.38 Fulton, D. A.;Gibson, C. L.
  11. Tetrahedron Lett. v.37 O'Brian, P.;Poumellec, P.
  12. J. Org. Chem. v.60 Miao, G;Rossiter, B. E.
  13. J. Chem. Soc., Chem. Commun. Toshimitsu, A.;Abo, H.;Hirosawa, C.;Tanimoto, S.
  14. J. Org. Chem. v.56 Chini, M.;Crotti, P.;Maccia, F.
  15. Synlett Niibo, Y.;Nakata, T.;Otera, J.;Nozaki, H.
  16. Tetrahedron Lett. v.28 De Lucci, O.;Buso, M.;Modena, G.
  17. Tetrahedron Lett. v.27 Atkins, R. K.;Frazier, J.;Moore, L. L.;Weigel, L. O.
  18. J. Org. Chem. v.59 Harris, C. E.;Fisher, G. B.;B.eardsley, D.;Lee, L.;Goralski, C. T.;Nicholson, L. W.;Singaram, B.
  19. Catalytic Asymmetric Synthesis Jacobsen, E. N.(Ed.);Ojima, I.(Ed.)
  20. Science v.261 Collman, J. P.;Zhang, X.;Lee, V. J.;Uffelman, E. S.;Brauman, J. I.
  21. J. Synth. Org. Chem. Jpn. v.53 Katsuki, T.
  22. J. Org. Chem. v.64 Wang, Z. X.;Miller, S. M.;Anderson, O. P.;Shi, Y.
  23. J. Am. Chem. Soc. v.119 Wang, Z. X.;Tu, Y.;Frohn, M.;Zhang, J. R.;Shi, Y.
  24. J. Am. Chem. Soc. v.112 Zhang, W.;Loebach, J. L.;Wilson, S. R.;Jacobsen, E. N.
  25. J. Org. Chem. v.56 Halterman, R. L.
  26. J. Am. Chem. Soc. v.115 Colman, J. P.;Lee, V. J.;Zhang, X.;Ibers, J. A.;Brauman, J. I.
  27. J. Am. Chem. Soc. v.113 Naruta, Y.;Tani, F.;Ishihara, N.;Maruyaman, K.
  28. J. Am. Chem. Soc. v.116 Palucki, M.;Pospicil, P. J.;Zhang, W.;Jacobsen, E. N.
  29. Tetrahedron v.53 For a review, see;Archer, I. B. J.
  30. J. Org. Chem. v.63 Moussou, P.;Archer, A.;Baratti, J.;Furstoss, R.
  31. Science v.2777 Tokunaga, M.;Larrow, J. F.;Kakiuchi, F.;Jacobsen, E. N.
  32. Tetrahedron: Asymmetry v.8 Brandes, B. D.;Jacobsen, E. N.
  33. J. Org. Chem. v.53 Corey, E. J.;Shibata, S.;Bakshi, R. K.
  34. Tetrahedron v.48 Kolb, H. C.;Sharpless, K. B.
  35. Org. Prep. Proced. Int. v.32 Choi, O. K.;Cho, B. T.
  36. J. Chem. Soc. Perkin Trans. v.1 Cho, B. T.;Yang, W. K.;Choi, O. K.
  37. Reductions in Organic Synthesis (ACS Symposium Series 641) For a recent review, see;Ramachandran, P. V.;Brown, H. C.;Abdel-Magid, A. F.(Ed.)
  38. J. Org. Chem. v.47 Koser, F. G.;Relenyi, A. G.;Kalos, A. N.;Revrovic, L.;Wettach, R. H.
  39. J. Org. Chem. v.53 Lodaya, J. S.;Koser, G. F.
  40. Synthesis Hoffman, R. V.
  41. Bull. Korean Chem. Soc. v.17 Lee, J. C.;Oh, Y. S.;Cho, S. H.
  42. Synlett and Tetrahedron Lett. Khanna, M. S.;Garg, C. P.;Kapoor, R. P.
  43. J. Org. Chem. v.57 Ramachandran, P. V.;Teodorovic, A. V.;Rangaishenvi, M. V.;Brown, H. C.
  44. J. Org. Chem. v.53 Corey, E. J.;Shibata, S.;Bakshi, R. K.
  45. Tetrahedron: Asymmetry v.9 Tanaka, K.;Yasuda, M.
  46. J. Org. Chem. v.61 Pedragosa-Moreau, S.;Morisseau, C.;Zylber, J.;Archelas, A.;Baratti, J.;Furstoss, R.
  47. Tetrahedron:Asymmetry v.11 Yvonne, G.;Archeles, A.;Broxterman, Q. B.;Schulze.;Furstoss, R.

피인용 문헌

  1. Facile Synthesis of Enantiopure 1,2-Diols and Terminal Epoxides from Chiral β-Hydroxy Sulfides vol.24, pp.7, 2003, https://doi.org/10.5012/bkcs.2003.24.7.1023
  2. Efficient Synthesis of Optically Active 2-N-Boc (or Cbz)-amino-1-arylethanols as Key Intermediates for Synthesis of Chiral Drugs via Asymmetric Reduction vol.25, pp.5, 2004, https://doi.org/10.5012/bkcs.2004.25.5.747