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Volumn 53, Issue 1, 1997, Pages 299-306

New syntheses of the Amaryllidacaea alkaloids vasconine, assoanine, oxoassoanine, pratosine and ismine by radical cyclisation

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ASSOANINE; ISMINE; OXOASSOANINE; PRATOSINE; UNCLASSIFIED DRUG; VASCONINE;

EID: 0031060463     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)00985-4     Document Type: Article
Times cited : (45)

References (27)
  • 5
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    • Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem., 1978, 21, 199. Pettit, G. R.; Gaddamidi, V.; Goswami, A.; Cragg, G. M. J. Nat. Prod., 1984, 47, 796. Chattopadhyay, S. C.; Chattopadhyay, U.; Mathur, P.; Saini, K. S. Planta Med., 1983, 49, 252.
    • (1978) J. Med. Chem. , vol.21 , pp. 199
    • Zee-Cheng, R.K.-Y.1    Yan, S.-J.2    Cheng, C.C.3
  • 6
    • 0021750466 scopus 로고
    • Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem., 1978, 21, 199. Pettit, G. R.; Gaddamidi, V.; Goswami, A.; Cragg, G. M. J. Nat. Prod., 1984, 47, 796. Chattopadhyay, S. C.; Chattopadhyay, U.; Mathur, P.; Saini, K. S. Planta Med., 1983, 49, 252.
    • (1984) J. Nat. Prod. , vol.47 , pp. 796
    • Pettit, G.R.1    Gaddamidi, V.2    Goswami, A.3    Cragg, G.M.4
  • 7
    • 0021050882 scopus 로고
    • Zee-Cheng, R. K.-Y.; Yan, S.-J.; Cheng, C. C. J. Med. Chem., 1978, 21, 199. Pettit, G. R.; Gaddamidi, V.; Goswami, A.; Cragg, G. M. J. Nat. Prod., 1984, 47, 796. Chattopadhyay, S. C.; Chattopadhyay, U.; Mathur, P.; Saini, K. S. Planta Med., 1983, 49, 252.
    • (1983) Planta Med. , vol.49 , pp. 252
    • Chattopadhyay, S.C.1    Chattopadhyay, U.2    Mathur, P.3    Saini, K.S.4
  • 18
    • 0342666524 scopus 로고    scopus 로고
    • Supplied by Aldrich Chem. Co. (Spain)
    • Supplied by Aldrich Chem. Co. (Spain).
  • 20
    • 0343100871 scopus 로고
    • For an alternative synthesis of ismine from N-norismine by N monomethylation of the latter see: Prabhakar, S.; Lobo, A. M.; Marques, M. M.; Tavares, M. R. J. Chem. Res. (S), 1985, 394. For other syntheses of ismine see: Hill, R. K.; Carlson, R. M. J. Org. Chem., 1965,30, 1571; Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett., 1988, 29, 5463.
    • (1985) J. Chem. Res. (S) , pp. 394
    • Prabhakar, S.1    Lobo, A.M.2    Marques, M.M.3    Tavares, M.R.4
  • 21
    • 0343972655 scopus 로고
    • For an alternative synthesis of ismine from N-norismine by N monomethylation of the latter see: Prabhakar, S.; Lobo, A. M.; Marques, M. M.; Tavares, M. R. J. Chem. Res. (S), 1985, 394. For other syntheses of ismine see: Hill, R. K.; Carlson, R. M. J. Org. Chem., 1965,30, 1571; Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett., 1988, 29, 5463.
    • (1965) J. Org. Chem. , vol.30 , pp. 1571
    • Hill, R.K.1    Carlson, R.M.2
  • 22
    • 0001186212 scopus 로고
    • For an alternative synthesis of ismine from N-norismine by N monomethylation of the latter see: Prabhakar, S.; Lobo, A. M.; Marques, M. M.; Tavares, M. R. J. Chem. Res. (S), 1985, 394. For other syntheses of ismine see: Hill, R. K.; Carlson, R. M. J. Org. Chem., 1965,30, 1571; Siddiqui, M. A.; Snieckus, V. Tetrahedron Lett., 1988, 29, 5463.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 5463
    • Siddiqui, M.A.1    Snieckus, V.2
  • 23
    • 0342666522 scopus 로고    scopus 로고
    • note
    • A blank experiment performed, under identical experimental conditions, showed that N-norismine was not converted into the phenanthridine 13.
  • 25
    • 0343536788 scopus 로고    scopus 로고
    • note
    • •.
  • 26
    • 77957058319 scopus 로고
    • Brossi, A. Ed.; Academic Press, New York
    • b) Formation of an aldehyde, in 9% yield, in a photochemicalIy induced cyclisation of a structurally more complex o-bromobenzylether has been reported: Bringmann, G.; In The Alkaloids', Brossi, A. Ed.; Academic Press, New York, 1986, Vol. 29; pp. 141.
    • (1986) The Alkaloids , vol.29 , pp. 141
    • Bringmann, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.