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Volumn 52, Issue 34, 1996, Pages 11361-11378

Total syntheses of tacamide-type indole alkaloids of Tabernaemontana eglandulosa

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE ALKALOID; NICOTINIC ACID DERIVATIVE; TACAMINE; TACAMONINE; UNCLASSIFIED DRUG;

EID: 0030593653     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00663-1     Document Type: Article
Times cited : (27)

References (31)
  • 1
    • 85030271196 scopus 로고    scopus 로고
    • Synthetic Studies Towards the Indole Alkaloid Tacamine, Part 4. For Part 3, see ref. 11
    • 1. Synthetic Studies Towards the Indole Alkaloid Tacamine, Part 4. For Part 3, see ref. 11.
  • 10
    • 77957033332 scopus 로고
    • Eburnamine-Vincamine Alkaloids
    • Cordell, G.A. Ed. Academic Press, New York
    • 8. Lounasmaa, M.; Tolvanen, A. Eburnamine-Vincamine Alkaloids in The Alkaloids (Cordell, G.A. Ed.), Vol. 42, Academic Press, New York, 1992, pp. 1-116.
    • (1992) The Alkaloids , vol.42 , pp. 1-116
    • Lounasmaa, M.1    Tolvanen, A.2
  • 16
    • 0011808396 scopus 로고
    • 14. (a) Lukeš, R.; Vaculík, P. Chem. Listy 1957, 57, 1510-1516 (Chem. Abstr. 1958, 52, 1163c);
    • (1957) Chem. Listy , vol.57 , pp. 1510-1516
    • Lukeš, R.1    Vaculík, P.2
  • 28
    • 85030268494 scopus 로고    scopus 로고
    • Protection of the hydroxyl group (e.g. as an acetate) leads to the loss of this moiety in the catalytic hydrogenation, possibly via the following mechanism: (formula presented)
    • 22. Protection of the hydroxyl group (e.g. as an acetate) leads to the loss of this moiety in the catalytic hydrogenation, possibly via the following mechanism: (formula presented)
  • 29
    • 85030280179 scopus 로고    scopus 로고
    • The complete NMR characterization of these diastereomeric alcohols, including determination of configuration at the hydroxyethyl side chain, will be reported elsewhere
    • 23. The complete NMR characterization of these diastereomeric alcohols, including determination of configuration at the hydroxyethyl side chain, will be reported elsewhere.
  • 31
    • 0011810157 scopus 로고
    • Atta-ur-Rahman, Ed. Elsevier, Amsterdam
    • 25. See e.g.: Lounasmaa, M. in Studies in Natural Products Chemistry (Atta-ur-Rahman, Ed.), Vol. 14, Elsevier, Amsterdam, 1994, p. 712.
    • (1994) Studies in Natural Products Chemistry , vol.14 , pp. 712
    • Lounasmaa, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.