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Volumn 43, Issue 10, 1996, Pages 2099-2112

A convenient access to protoberberine derivatives

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[No Author keywords available]

Indexed keywords


EID: 0010729208     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-96-7439     Document Type: Article
Times cited : (5)

References (32)
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    • 0025770727 scopus 로고
    • See for example: a) D. L. C. McCall, J. Alexander, J. Barber, R.G. Jaouhari, A. Satoskar, and R. D. Waigh, Bioorg.& Med. Chem. Lett., 1994, 4, 1663; b) C. Weimar, S. Angerer, and W. Wiegrebe, Arch. Pharm. (Wienheim), 1991, 324, 509; c) S. Angerer, G. Brandl, A. Mannschreck, C. Weimar, and W. Wiegrebe, Anti-Cancer Drug Design, 1992, 7, 351.
    • (1991) Arch. Pharm. (Wienheim) , vol.324 , pp. 509
    • Weimar, C.1    Angerer, S.2    Wiegrebe, W.3
  • 3
    • 0026658263 scopus 로고
    • See for example: a) D. L. C. McCall, J. Alexander, J. Barber, R.G. Jaouhari, A. Satoskar, and R. D. Waigh, Bioorg.& Med. Chem. Lett., 1994, 4, 1663; b) C. Weimar, S. Angerer, and W. Wiegrebe, Arch. Pharm. (Wienheim), 1991, 324, 509; c) S. Angerer, G. Brandl, A. Mannschreck, C. Weimar, and W. Wiegrebe, Anti-Cancer Drug Design, 1992, 7, 351.
    • (1992) Anti-Cancer Drug Design , vol.7 , pp. 351
    • Angerer, S.1    Brandl, G.2    Mannschreck, A.3    Weimar, C.4    Wiegrebe, W.5
  • 12
    • 0009802153 scopus 로고
    • See for example a) S. F. Dyke, D. W. Brown, M. Sainsbury, and G. Hardy, Tetrahedron, 1971, 27, 3495; b) S. F. Dyke and E. P. Tiley, Tetrahedron, 1975, 31, 561; c) D. Badía, E. Domínguez, and C. Iriondo, J. Heterocycl. Chem., 1986, 23, 1599.
    • (1971) Tetrahedron , vol.27 , pp. 3495
    • Dyke, S.F.1    Brown, D.W.2    Sainsbury, M.3    Hardy, G.4
  • 13
    • 0000969795 scopus 로고
    • See for example a) S. F. Dyke, D. W. Brown, M. Sainsbury, and G. Hardy, Tetrahedron, 1971, 27, 3495; b) S. F. Dyke and E. P. Tiley, Tetrahedron, 1975, 31, 561; c) D. Badía, E. Domínguez, and C. Iriondo, J. Heterocycl. Chem., 1986, 23, 1599.
    • (1975) Tetrahedron , vol.31 , pp. 561
    • Dyke, S.F.1    Tiley, E.P.2
  • 14
    • 25744465098 scopus 로고
    • See for example a) S. F. Dyke, D. W. Brown, M. Sainsbury, and G. Hardy, Tetrahedron, 1971, 27, 3495; b) S. F. Dyke and E. P. Tiley, Tetrahedron, 1975, 31, 561; c) D. Badía, E. Domínguez, and C. Iriondo, J. Heterocycl. Chem., 1986, 23, 1599.
    • (1986) J. Heterocycl. Chem. , vol.23 , pp. 1599
    • Badía, D.1    Domínguez, E.2    Iriondo, C.3
  • 15
    • 2742565528 scopus 로고    scopus 로고
    • note
    • -1) 3400-3250 (NH st.). Satisfactory combustion analyses were obtained for tetrahydroisoquinolines (4a) and (4b).
  • 21
    • 0001739614 scopus 로고
    • The synthesis of isoquinolines by the Pomeranz-Fritsch reaction
    • W. J. Gensler, "The synthesis of isoquinolines by the Pomeranz-Fritsch reaction", Organic Reactions, 1951, vol. 6, p. 191.
    • (1951) Organic Reactions , vol.6 , pp. 191
    • Gensler, W.J.1
  • 24
    • 2742552445 scopus 로고
    • Ph. D. Thesis, University of the Basque Country
    • I. Tellitu, Ph. D. Thesis, University of the Basque Country, 1994.
    • (1994)
    • Tellitu, I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.