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Volumn 9, Issue 2, 2007, Pages 295-298

First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridme and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A

Author keywords

[No Author keywords available]

Indexed keywords

16 EPI VELLOSIMINE; 16-EPI-VELLOSIMINE; ALDEHYDE; ALKALOID; INDOLE ALKALOID; MACUSINE A; POLYNEURIDINE; POLYNEURIDINE ALDEHYDE; UNCLASSIFIED DRUG;

EID: 33846623329     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol062762q     Document Type: Article
Times cited : (27)

References (36)
  • 2
    • 0002452680 scopus 로고
    • The Synthesis of Macroline Related Alkaloids
    • Pelletier, S. W, Ed, Elsevier Science: New York
    • Hamaker, L. K.; Cook, J. M. The Synthesis of Macroline Related Alkaloids. In Alkaloids: Chemical and Biological Perspectives; Pelletier, S. W., Ed.; Elsevier Science: New York, 1995; Vol. 9, pp 23-84.
    • (1995) Alkaloids: Chemical and Biological Perspectives , vol.9 , pp. 23-84
    • Hamaker, L.K.1    Cook, J.M.2
  • 3
    • 0035238311 scopus 로고    scopus 로고
    • The Ajmaline Group of Indole Alkaloids
    • Cordell, G. A, Ed, Academic Press: San Diego, Chapter 1, pp
    • Lounasmaa, M.; Hanhinen, P. The Ajmaline Group of Indole Alkaloids. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: San Diego, 2001; Vol. 55, Chapter 1, pp 1-87.
    • (2001) The Alkaloids , vol.55 , pp. 1-87
    • Lounasmaa, M.1    Hanhinen, P.2
  • 6
    • 0013848559 scopus 로고
    • The biogenetic numbering of indole alkaloids is used in the text. See
    • The "biogenetic numbering" of indole alkaloids is used in the text. See: Le Men, J.; Taylor, W. I. Experientia 1965, 21, 508.
    • (1965) Experientia , vol.21 , pp. 508
    • Le Men, J.1    Taylor, W.I.2
  • 17
    • 0015581781 scopus 로고    scopus 로고
    • Quebrachidine 4 was reported to show psychosedative and adrenergic activity. See: Lyon, R. L.; Fong, H. H. S.; Farnsworth, N. R.; Svoboda, G. H. J. Pharm. Sci. 1973, 62, 218.
    • Quebrachidine 4 was reported to show psychosedative and adrenergic activity. See: Lyon, R. L.; Fong, H. H. S.; Farnsworth, N. R.; Svoboda, G. H. J. Pharm. Sci. 1973, 62, 218.
  • 18
    • 0000834750 scopus 로고    scopus 로고
    • Biomimetic synthesis of 7 from 6. See: Burke, D. E.; Cook, J. M.; Le Quesne, P. W. J. Am. Chem. Soc. 1973, 95, 546.
    • Biomimetic synthesis of 7 from 6. See: Burke, D. E.; Cook, J. M.; Le Quesne, P. W. J. Am. Chem. Soc. 1973, 95, 546.
  • 19
    • 0032714668 scopus 로고    scopus 로고
    • Antimalarial activity: (a) Keawpradub, N.; Kirby, G. C.; Steele, J. C.; Houghton, P. J. Planta Med. 1999, 65, 690.
    • Antimalarial activity: (a) Keawpradub, N.; Kirby, G. C.; Steele, J. C.; Houghton, P. J. Planta Med. 1999, 65, 690.
  • 33
    • 0027997412 scopus 로고    scopus 로고
    • For a review on TPAP/NMO oxidations, see: Ley, S. V.; Norman, J.; Griffith, W. P.; Marsden, S. P. Synthesis 1994, 23, 639.
    • For a review on TPAP/NMO oxidations, see: Ley, S. V.; Norman, J.; Griffith, W. P.; Marsden, S. P. Synthesis 1994, 23, 639.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.