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Volumn 65, Issue 11, 2009, Pages 2201-2211

Synthesis of a novel tetrahydroisoquinoline pentacyclic framework

Author keywords

Antitumor antibiotics; N Acyliminium; Pictet Spengler type; Tetrahydroisoquinolines

Indexed keywords

3 METHYL PYRAZINOL[1,2 B]ISOQUINOLINE 1,4 DIONE DERIVATIVE; ENAMINE; QUINOLINE DERIVATIVE; TETRAHYDROISOQUINOLINE; UNCLASSIFIED DRUG;

EID: 59749100522     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.01.051     Document Type: Article
Times cited : (17)

References (26)
  • 12
    • 59749104761 scopus 로고    scopus 로고
    • Avendaño, C.; de la Cuesta, E. Curr. Org. Synth., in press.
    • Avendaño, C.; de la Cuesta, E. Curr. Org. Synth., in press.
  • 19
    • 59749105205 scopus 로고    scopus 로고
    • note
    • 2O.
  • 20
    • 49549155653 scopus 로고
    • This type of oxidation process is very common in simple enolizable ketones. See for instance:
    • This type of oxidation process is very common in simple enolizable ketones. See for instance:. Fetizon M., Kakis F.J., and Ignatioadou-Ragoussis V. Tetrahedron 30 (1974) 3981-3989
    • (1974) Tetrahedron , vol.30 , pp. 3981-3989
    • Fetizon, M.1    Kakis, F.J.2    Ignatioadou-Ragoussis, V.3
  • 22
    • 0001974818 scopus 로고
    • For a general review on diimide reductions, see:. Paquette L.A. (Ed), John Wiley & Sons, New York, NY
    • For a general review on diimide reductions, see:. Pasto D.J., and Taylor R.T. In: Paquette L.A. (Ed). Organic Reactions (1991), John Wiley & Sons, New York, NY 91-155
    • (1991) Organic Reactions , pp. 91-155
    • Pasto, D.J.1    Taylor, R.T.2
  • 23
    • 34247257366 scopus 로고    scopus 로고
    • For reduction of solid-supported multiple bonded substrates, see:
    • For reduction of solid-supported multiple bonded substrates, see:. Buszek K.R., and Brown N. J. Org. Chem. 72 (2007) 3125-3128
    • (2007) J. Org. Chem. , vol.72 , pp. 3125-3128
    • Buszek, K.R.1    Brown, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.