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Volumn 61, Issue 10, 2003, Pages 949-960

Total Synthesis of Potent Antitumor Alkaloid Ecteinascidin 743

Author keywords

Chiral template; DuPHOS; Ecteinascidin 743; Intramolecular Heck reaction; Phase II and III clinical trials; Phenol aldehyde cyclization; Pictet Spengler reaction; Potent antitumor alkaloid; Tetrahydroisoquinoline; Ugi's 4 CC reaction

Indexed keywords

DRUG PRODUCTS; HYDROGENATION; MOLECULAR DYNAMICS; ONCOLOGY; OXIDATION; PHENOLS; SILVER COMPOUNDS; SYNTHESIS (CHEMICAL); TUMORS;

EID: 0346329883     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: 10.5059/yukigoseikyokaishi.61.949     Document Type: Article
Times cited : (9)

References (41)
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    • Scott, J.D.1    Williams, R.M.2
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    • 0001218910 scopus 로고
    • A similar difference of reactivity in the D-glucose derivatives was reported: G. W. J. Fleet, P. W. Smith, Tetrahedron, 43, 971 (1987)
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    • Fleet, G.W.J.1    Smith, P.W.2
  • 27
    • 0002654419 scopus 로고    scopus 로고
    • F. Diederich, P. J. Stang, Eds., Wiley-VCH Verlag GmbH, Weinheim, Germany
    • For reviews, see: (a) J. T. Link, L. E. Overman, "In Metal-Catalyzed Cross-Coupling Reactions" F. Diederich, P. J. Stang, Eds., Wiley-VCH Verlag GmbH, Weinheim, Germany, 231 (1998)
    • (1998) In Metal-Catalyzed Cross-Coupling Reactions , pp. 231
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  • 31
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    • In Isonitrile Chemistry
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    • 1971 , pp. 145
    • Gokel, G.1    Lüdke, G.2    Ugi, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.