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Volumn , Issue 7, 2001, Pages 660-661

An expeditious synthesis of optically pure 1,4,5,6-tetrahydro-as-triazines, fused to the carbohydrate skeleton

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EID: 0035634154     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2001.660     Document Type: Article
Times cited : (9)

References (19)
  • 1
    • 0003790195 scopus 로고    scopus 로고
    • ed. by Y. Chapleur, Wiley-VCH, Weinheim, and relevant references cited therein
    • Y. Chapleur, in "Carbohydrate Mimics: Concepts and Methods," ed. by Y. Chapleur, Wiley-VCH, Weinheim (1997), and relevant references cited therein.
    • (1997) Carbohydrate Mimics: Concepts and Methods
    • Chapleur, Y.1
  • 6
    • 0040763841 scopus 로고    scopus 로고
    • U. S. Patent 3510483 (1967)
    • D. L. Trepanier, U. S. Patent 3510483 (1967); Chem. Abstr., 73, 35415y (1970).
    • Trepanier, D.L.1
  • 7
    • 4243841674 scopus 로고
    • D. L. Trepanier, U. S. Patent 3510483 (1967); Chem. Abstr., 73, 35415y (1970).
    • (1970) Chem. Abstr. , vol.73
  • 8
    • 0038985655 scopus 로고    scopus 로고
    • U. S. Patent 3428635 (1966)
    • D. L. Trepanier, G. H. Harris, U. S. Patent 3428635 (1966); Chem. Abstr., 71, 81438q (1969).
    • Trepanier, D.L.1    Harris, G.H.2
  • 9
    • 25344450485 scopus 로고
    • D. L. Trepanier, G. H. Harris, U. S. Patent 3428635 (1966); Chem. Abstr., 71, 81438q (1969).
    • (1969) Chem. Abstr. , vol.71
  • 10
    • 0039578334 scopus 로고    scopus 로고
    • U. S. Patent 3462431 (1966)
    • E. R. Wagner, U. S. Patent 3462431 (1966); Chem. Abstr., 71, 91541g (1969).
    • Wagner, E.R.1
  • 11
    • 4243557983 scopus 로고
    • E. R. Wagner, U. S. Patent 3462431 (1966); Chem. Abstr., 71, 91541g (1969).
    • (1969) Chem. Abstr. , vol.71
  • 18
    • 0038985645 scopus 로고    scopus 로고
    • note
    • 3) data of 5a: δ (ppm) 7.40-7.44 (2H, m, PhH), 7.26-7.32 (7H, m, PhH), 6.90 (1H, m, PhH), 5.54 (1H, s, NH), 4.88 (1H, d, J = 11.5 Hz, PhCHH), 4.59 (1H, d, J= 11.5 Hz, PhCHH), 4.42 (1H, d, J= 7.77 Hz, H-1), 3.84 (1H, dd, J = 3.35 and 9.7 Hz, H-3), 4.07 (1H, dd, J = 1.5 and 13.13 Hz, H-5), 3.76 (1H, dd, J = 1.5 and 13.13 Hz, H-5′), 3.55 (1H, dd, J = 7.9 and 9.7 Hz, H-2), 3.43 (1H, brs, H-4), 2.5 (3H, s, OMe); 5b: 7.33 (7H, m, PhH), 6.86 (2H, m, PhH), 5.50 (1H, s, NH), 5.29 (3H, s, OMe), 4.90 (1H, d, J = 11.6 Hz, PhCHH), 4.62 (1H, d, J = 11.6 Hz, PhCHW), 4.41 (1H, d, J = 9.7 Hz, H-1), 4.08 (1H, d, J = 12.8 Hz, H-5), 3.77 (3H, m, H-2, H-3, H-5′), 2.5 (3H, s, OMe); 5c: 7.25-7.37 (2H, m, PhH), 7.29 (5H, m, PhH), 6.98 (2H, m, PhW), 5.55 (1H, s, NH), 4.87 (1H, d, J = 11.6 Hz, PhCHH), 4.57 (1H, d, J = 11.6 Hz, PhCHH), 4.40 (1H, d, J = 7.63 Hz, H-1), 4.22 (1H, dd, J = 3.36 and 9.76 Hz, H-3), 4.06 (1H, dd, J = 1.53 and 13.12Hz, H-5), 3.75 (1H, dd, 7= 1.53 and 13.12 Hz, H-5′), 3.52 (1H, dd, J = 7.63 and 9.76 Hz, H-2), 3.42 (1H, m, H-4), 2.5 (3H, s, OMe); 5d: 7.42-7.43 (2H, m, PhH), 7.13-7.42 (5H, m, PhH), 6.83-6.86 (2H, m, PhH), 5.73 (1H, s, NH), 4.81 (1H, d, J = 11.3 Hz, PhCHH), 4.50 (1H, d, J = 11.3 Hz, PhCHH), 4.37 (1H, d, J = 7.94 Hz, H-1), 4.24 (1H, dd, J = 2.74 and 9.76 Hz, H-3), 4.02 (1H, d, J = 13.12 Hz, H-5), 3.69 (1H, d, 13.12 Hz, H-5′), 3.54 (2H, m, H-2, H-4), 2.5 (3H, s, OMe).
  • 19
    • 0040763836 scopus 로고    scopus 로고
    • note
    • 3).


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