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Volumn 44, Issue 8, 1996, Pages 1631-1633

Alternative synthesis of duocarmycin SA using a tricyclic heteroaromatic intermediate prepared by palladium-catalyzed coupling reactions

Author keywords

3H pyrrolo 3,2 f quinoline derivative; antitumor antibiotic; duocarmycin SA; formal synthesis; palladium catalyzed coupling

Indexed keywords

ANTINEOPLASTIC ANTIBIOTIC; DUOCARMYCIN A; DUOCARMYCIN B1; DUOCARMYCIN B2; DUOCARMYCIN SA; PALLADIUM; PYRINDAMYCIN A; PYRINDAMYCIN B; QUINOLINE DERIVATIVE; RACHELMYCIN; UNCLASSIFIED DRUG;

EID: 0029760961     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.44.1631     Document Type: Article
Times cited : (18)

References (28)
  • 24
    • 0026699017 scopus 로고    scopus 로고
    • Review: a) Stille J. K., Angew. Chem., Int. Ed. Engl., 15, 508-524 (1986); b) Mitchell T. N., Synthesis, 1992, 803-815.
    • Synthesis , vol.1992 , pp. 803-815
    • Mitchell, T.N.1
  • 27
    • 0001403744 scopus 로고
    • Alcohols 10a and 10b were formed by addition of borane generated in situ to 5a and 5b, followed by oxidation with air. cf. Brown H. C., Midland M. M., Kabalka G. W., J. Am. Chem. Soc., 93, 1024-1025 (1971).
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 1024-1025
    • Brown, H.C.1    Midland, M.M.2    Kabalka, G.W.3
  • 28
    • 9544235249 scopus 로고    scopus 로고
    • note
    • Thanks are due to the Ministry of Education, Science, and Culture of Japan for financial support.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.