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Volumn , Issue 2, 1999, Pages 216-218

First total synthesis of dioncophylline B, a 7,6'-coupled naphthylisoquinoline alkaloid

Author keywords

Cross coupling; Dioncophylline B; Directed ortho metalation; Naphthylisoquinoline alkaloids; Total synthesis

Indexed keywords

DIONCOPYLLINE B; ISOQUINOLINE DERIVATIVE; METAL; UNCLASSIFIED DRUG;

EID: 0344141328     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2575     Document Type: Article
Times cited : (14)

References (38)
  • 2
    • 77957089074 scopus 로고
    • Cordell, G.A., Ed.; Academic Press: New York
    • For reviews, see: a) Bringmann, G.; Pokorny, F. In The Alkaloids, Vol. 46; Cordell, G.A., Ed.; Academic Press: New York, 1995; p 127.
    • (1995) The Alkaloids , vol.46 , pp. 127
    • Bringmann, G.1    Pokorny, F.2
  • 11
  • 13
    • 0003486057 scopus 로고    scopus 로고
    • Scolastico, C.; Nicotra, F., Eds.; Plenum Publishing Corporation: New York, in press
    • a) Bringmann, G.; Tasler, S. In Current Trends in Organic Synthesis; Scolastico, C.; Nicotra, F., Eds.; Plenum Publishing Corporation: New York, in press.
    • Current Trends in Organic Synthesis
    • Bringmann, G.1    Tasler, S.2
  • 17
    • 0344643462 scopus 로고    scopus 로고
    • 11c,d
    • 11c,d
  • 18
    • 0012397313 scopus 로고
    • For reviews, see: a) Snieckus, V. Chem. Rev. 1990, 90, 879.
    • (1990) Chem. Rev. , vol.90 , pp. 879
    • Snieckus, V.1
  • 19
    • 0003171828 scopus 로고    scopus 로고
    • Chatgilialoglu, C.; Snieckus, V., Ed.; Kluwer Academic Publishers: Netherlands
    • b) Snieckus, V. In: Chemical Synthesis; Chatgilialoglu, C.; Snieckus, V., Ed.; Kluwer Academic Publishers: Netherlands, 1996, p 191.
    • (1996) Chemical Synthesis , pp. 191
    • Snieckus, V.1
  • 20
    • 0001210050 scopus 로고
    • For a (stepwise) double DoM → biaryl cross-coupling to give m-ter- and tetraphenyls, see Sharp, M.J.; Cheng, W.; Sniekkus, V. Tetrahedron Lett. 1987, 28, 5093 and Cheng, W.; Snieckus, V. Tetrahedron Lett. 1987, 28, 5097. See also James, C.A.; Snieckus, V. Tetrahedron Lett. 1997, 38, 8149.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5093
    • Sharp, M.J.1    Cheng, W.2    Sniekkus, V.3
  • 21
    • 0001197152 scopus 로고
    • For a (stepwise) double DoM → biaryl cross-coupling to give m-ter- and tetraphenyls, see Sharp, M.J.; Cheng, W.; Sniekkus, V. Tetrahedron Lett. 1987, 28, 5093 and Cheng, W.; Snieckus, V. Tetrahedron Lett. 1987, 28, 5097. See also James, C.A.; Snieckus, V. Tetrahedron Lett. 1997, 38, 8149.
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5097
    • Cheng, W.1    Snieckus, V.2
  • 22
    • 0030683497 scopus 로고    scopus 로고
    • For a (stepwise) double DoM → biaryl cross-coupling to give m-ter- and tetraphenyls, see Sharp, M.J.; Cheng, W.; Sniekkus, V. Tetrahedron Lett. 1987, 28, 5093 and Cheng, W.; Snieckus, V. Tetrahedron Lett. 1987, 28, 5097. See also James, C.A.; Snieckus, V. Tetrahedron Lett. 1997, 38, 8149.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8149
    • James, C.A.1    Snieckus, V.2
  • 33
    • 0000103227 scopus 로고
    • For reviews, see: a) Stille, J.K. Angew. Chem. 1986, 98, 504; Angew. Chem., Int. Ed. Engl. 1986, 25, 508.
    • (1986) Angew. Chem. , vol.98 , pp. 504
    • Stille, J.K.1
  • 34
    • 84985570392 scopus 로고
    • For reviews, see: a) Stille, J.K. Angew. Chem. 1986, 98, 504; Angew. Chem., Int. Ed. Engl. 1986, 25, 508.
    • (1986) Angew. Chem., Int. Ed. Engl. , vol.25 , pp. 508
  • 38
    • 0345505699 scopus 로고    scopus 로고
    • In addition, smaller amounts of 6 and 4 were detected
    • In addition, smaller amounts of 6 and 4 were detected.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.