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Volumn 7, Issue 12, 1996, Pages 3431-3444

Asymmetric synthesis with diphenylphosphine oxides: Bicyclic aminals and oxazolidines as chiral auxiliaries

Author keywords

[No Author keywords available]

Indexed keywords

NOREPHEDRINE; OXAZOLIDINE DERIVATIVE; PHOSPHINE OXIDE DERIVATIVE;

EID: 0030561470     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(96)00451-X     Document Type: Article
Times cited : (12)

References (49)
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    • note
    • 2) and the hydroxyl group as drawn.
  • 31
    • 0026459980 scopus 로고
    • 24. For a review on the use of cyclic sulfates and sulfites in synthesis, see: Lohray, B. B. Synthesis, 1992, 1035-1052; Kolb, H. C.; VanNieuwenhze, M. S.; Sharpless, K. B. Chem. Rev., 1994, 94, 2483-2547.
    • (1992) Synthesis , pp. 1035-1052
    • Lohray, B.B.1
  • 32
    • 4444276636 scopus 로고
    • 24. For a review on the use of cyclic sulfates and sulfites in synthesis, see: Lohray, B. B. Synthesis, 1992, 1035-1052; Kolb, H. C.; VanNieuwenhze, M. S.; Sharpless, K. B. Chem. Rev., 1994, 94, 2483-2547.
    • (1994) Chem. Rev. , vol.94 , pp. 2483-2547
    • Kolb, H.C.1    VanNieuwenhze, M.S.2    Sharpless, K.B.3
  • 39
    • 0000870492 scopus 로고
    • 31. He, X-C.; Eliel, E. L. Tetrahedron, 1987, 43, 4979-4987. See also: Matsubara, S.; Takahashi, H.; Utimoto, K. Chem. Lett., 1992, 2173-2176.
    • (1987) Tetrahedron , vol.43 , pp. 4979-4987
    • He, X.-C.1    Eliel, E.L.2
  • 43
    • 33947094130 scopus 로고
    • 34. Luche, J-L. J. Am. Chem. Soc., 1978, 100, 2226-2227; Gemal, A. L.; Luche, J-L. J. Am. Chem. Soc., 1981, 103, 5454-5459.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 2226-2227
    • Luche, J.-L.1
  • 44
    • 33845556313 scopus 로고
    • 34. Luche, J-L. J. Am. Chem. Soc., 1978, 100, 2226-2227; Gemal, A. L.; Luche, J-L. J. Am. Chem. Soc., 1981, 103, 5454-5459.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 5454-5459
    • Gemal, A.L.1    Luche, J.-L.2
  • 45
    • 0011952953 scopus 로고    scopus 로고
    • note
    • 35. Hoppe has suggested a similar Felkin transition state to rationalise the stereoselectivity of additions to some structurally related keto oxazolidines (see reference 12a).
  • 46
    • 0028803867 scopus 로고
    • Chelation of cerium between ketone and phosphinoyl oxygens in Luche reductions is of course well established
    • 36. Chelation of cerium between ketone and phosphinoyl oxygens in Luche reductions is of course well established: Hutton, G.; Jolliff, T.; Mitchell, H.; Warren, S. Tetrahedron Lett., 1995, 36, 7905-7908.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 7905-7908
    • Hutton, G.1    Jolliff, T.2    Mitchell, H.3    Warren, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.