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Volumn 39, Issue 17, 1998, Pages 2451-2454

A direct connection of a tricyclic analog of methyllycaconitine with 2- methylsuccinimidobenzoic acid

Author keywords

[No Author keywords available]

Indexed keywords

2 METHYLSUCCINIMIDOBENZOIC ACID; ALPHA BUNGAROTOXIN; METHYLLYCACONITINE; NICOTINIC RECEPTOR; UNCLASSIFIED DRUG;

EID: 0032560052     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00239-1     Document Type: Article
Times cited : (25)

References (17)
  • 1
    • 0002603630 scopus 로고
    • 1. Manske, R. H. F. Can. J. Research, 1938, 16B, 57. Pelletier, S. W.; Mody, N. V.; Joshi, B. S.; Schramm, L. C. Alkaloids: Chemical and Biological Perspectives: Pelletier, S. W., ed., J. Wiley and Sons, New York, 1984, 2, 205. Yusunov, M. S. Nat. Prod. Rep., 1991, 8, 499.
    • (1938) Can. J. Research , vol.16 B , pp. 57
    • Manske, R.H.F.1
  • 3
    • 0010624811 scopus 로고
    • 1. Manske, R. H. F. Can. J. Research, 1938, 16B, 57. Pelletier, S. W.; Mody, N. V.; Joshi, B. S.; Schramm, L. C. Alkaloids: Chemical and Biological Perspectives: Pelletier, S. W., ed., J. Wiley and Sons, New York, 1984, 2, 205. Yusunov, M. S. Nat. Prod. Rep., 1991, 8, 499.
    • (1991) Nat. Prod. Rep. , vol.8 , pp. 499
    • Yusunov, M.S.1
  • 14
    • 0010553227 scopus 로고
    • For a better procedure
    • 11. Whitehurst, J. S.; Dave, V. J. C. S. Perkin Trans. 1, 1973, 393. For a better procedure, see: Eaton, P. E.; Jobe, P. G. Synthesis, 1983, 796.
    • (1973) J. C. S. Perkin Trans. 1 , pp. 393
    • Whitehurst, J.S.1    Dave, V.2
  • 15
    • 0010590159 scopus 로고
    • 11. Whitehurst, J. S.; Dave, V. J. C. S. Perkin Trans. 1, 1973, 393. For a better procedure, see: Eaton, P. E.; Jobe, P. G. Synthesis, 1983, 796.
    • (1983) Synthesis , pp. 796
    • Eaton, P.E.1    Jobe, P.G.2
  • 17
    • 84920293505 scopus 로고    scopus 로고
    • note
    • 3) δ 12.8, 16.3, 20.5, 34.0, 35.2, 36.6, 36.8, 37.0, 37.2, 38.1, 39.1, 41.0, 41.3, 47.2, 48.2, 61.5, 63.2, 73.8, 89.0, 129.3, 132.3, 132.4, 132.7, 132.9, 133.0, 176.8, 180.2, 180.9.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.