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Volumn 7, Issue 10, 2005, Pages 2031-2033

Cascade iminium ion reactions for the facile synthesis of quinolizidines. Concise syntheses of (±)-epilupinine and (-)-epimyrtine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID DERIVATIVE; EPIMYRTINE; IMINE; LUPININE; QUINOLIZIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 19544382355     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol050544b     Document Type: Article
Times cited : (48)

References (41)
  • 1
    • 7044235263 scopus 로고    scopus 로고
    • For reviews, see: (a) Tietze, L. F. Chem. Rev. 1996, 96, 115.
    • (1996) Chem. Rev. , vol.96 , pp. 115
    • Tietze, L.F.1
  • 4
    • 7744232650 scopus 로고    scopus 로고
    • For a leading review of indolizidine and quinolizidine alkaloids, see: Michael, J. P. Nat. Prod. Rep. 2004, 21, 625.
    • (2004) Nat. Prod. Rep. , vol.21 , pp. 625
    • Michael, J.P.1
  • 29
    • 3142683132 scopus 로고    scopus 로고
    • 13C NMR spectral data for synthetic 14 were consistent with those reported. See: Ma, S.; Ni, B. Eur. J. Chem. 2004, 10, 3286.
    • (2004) Eur. J. Chem. , vol.10 , pp. 3286
    • Ma, S.1    Ni, B.2
  • 32
    • 19544389034 scopus 로고    scopus 로고
    • note
    • 3CN or upon heating in the presence of basic alumina.
  • 37
    • 0003244794 scopus 로고
    • Stereoelectronic Effects in Organic Chemistry
    • Pergamon Press: New York
    • (c) Deslongchamps, P. Stereoelectronic Effects in Organic Chemistry; Organic Chemistry Series, Vol. 1; Pergamon Press: New York, 1983.
    • (1983) Organic Chemistry Series , vol.1
    • Deslongchamps, P.1
  • 39
    • 0001258881 scopus 로고
    • 13C NMR spectral data for synthetic 23 and 24 and the specific rotation for 23 were consistent with those reported. See: (a) Slosse, P.; Hootele, C. Tetrahedron 1981, 37, 4287.
    • (1981) Tetrahedron , vol.37 , pp. 4287
    • Slosse, P.1    Hootele, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.