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Volumn 37, Issue 17, 1996, Pages 3051-3054

Norephedrine-derived oxazolidines as chiral auxiliaries-stereocontrolled routes to R or S β-hydroxy phosphine oxides

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHINE OXIDE DERIVATIVE;

EID: 0029998934     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00467-4     Document Type: Article
Times cited : (15)

References (31)
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    • note
    • β-Keto phosphine oxide 9 was synthesised in 52% yield using an acylation reaction between lithiated methyldiphenylphosphine oxide and methyl ester 6.
  • 4
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    • He, X-C.; Eliel, E. L. Tetrahedron, 1987, 43, 4979-4987. See also: Matsubara, S.; Takahashi, H.; Utimoto, K. Chem. Lett., 1992, 2173-2176.
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  • 9
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    • Agami, C.; Couty, F.; Lequesne, C Tetrahedron, 1995, 51, 4043-4056; Agami, C.; Couty, F.; Lequesne, C. Tetrahedron Lett., 1994, 35, 3309-3312; Colombo, L.; Di Giacomo, M.; Brusotti, G.; Delogu, G. Tetrahedon Lett., 1994, 35, 2063-2066.
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    • Agami, C.1    Couty, F.2    Lequesne, C.3
  • 10
    • 0028240876 scopus 로고
    • Agami, C.; Couty, F.; Lequesne, C Tetrahedron, 1995, 51, 4043-4056; Agami, C.; Couty, F.; Lequesne, C. Tetrahedron Lett., 1994, 35, 3309-3312; Colombo, L.; Di Giacomo, M.; Brusotti, G.; Delogu, G. Tetrahedon Lett., 1994, 35, 2063-2066.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 3309-3312
    • Agami, C.1    Couty, F.2    Lequesne, C.3
  • 11
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    • Agami, C.; Couty, F.; Lequesne, C Tetrahedron, 1995, 51, 4043-4056; Agami, C.; Couty, F.; Lequesne, C. Tetrahedron Lett., 1994, 35, 3309-3312; Colombo, L.; Di Giacomo, M.; Brusotti, G.; Delogu, G. Tetrahedon Lett., 1994, 35, 2063-2066.
    • (1994) Tetrahedon Lett. , vol.35 , pp. 2063-2066
    • Colombo, L.1    Di Giacomo, M.2    Brusotti, G.3    Delogu, G.4
  • 14
    • 85030186798 scopus 로고    scopus 로고
    • note
    • Scolastico synthesised essentially the same ratio of 1,2 diols syn- and anti-11 in 80% yield using a slightly different dihydroxylation procedure (see reference 6).
  • 15
    • 85030191884 scopus 로고    scopus 로고
    • note
    • 2) and the hydroxyl group as drawn.
  • 19
    • 0026459980 scopus 로고
    • 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
  • 20
    • 4444276636 scopus 로고
    • 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
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    • (1993) J. Org. Chem. , vol.58 , pp. 5832-5837
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    • (1995) Tetrahedron Lett. , vol.36 , pp. 8473-8476
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    • 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.
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    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 5454-5459
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.