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Volumn 65, Issue 33, 2009, Pages 6591-6599

Synthesis and preliminary evaluation of duocarmycin analogues incorporating the 1,2,11,11a-tetrahydrocyclopropa[c]naphtho[2,3-e]indol-4-one (CNI) and 1,2,11,11a-tetrahydrocyclopropa[c]naphtho[1,2-e]indol-4-one (iso-CNI) alkylation subunits

Author keywords

[No Author keywords available]

Indexed keywords

1,2,11,11A TETRAHYDROCYCLOPROPA[C]NAPHTHO[1,2 E]INDOL 4 ONE; 1,2,11,11A TETRAHYDROCYCLOPROPA[C]NAPHTHO[2,3 E]INDOL 4 ONE; ANTHRACENE DERIVATIVE; DUOCARMYCIN DERIVATIVE; PHENANTHRENE DERIVATIVE; RACHELMYCIN; UNCLASSIFIED DRUG;

EID: 67650260769     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.02.065     Document Type: Article
Times cited : (9)

References (71)
  • 2
    • 0028376605 scopus 로고
    • For a detailed discussion of the DNA alkylation selectivity of CC-1065, see:
    • For a detailed discussion of the DNA alkylation selectivity of CC-1065, see:. Boger D.L., Johnson D.S., Yun W., and Tarby C.M. Bioorg. Med. Chem. 2 (1994) 115
    • (1994) Bioorg. Med. Chem. , vol.2 , pp. 115
    • Boger, D.L.1    Johnson, D.S.2    Yun, W.3    Tarby, C.M.4
  • 10
    • 0028095610 scopus 로고
    • Duocarmycin SA DNA alkylation properties:
    • Duocarmycin SA DNA alkylation properties:. Boger D.L., Johnson D.S., and Yun W. J. Am. Chem. Soc. 116 (1994) 1635
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 1635
    • Boger, D.L.1    Johnson, D.S.2    Yun, W.3
  • 61
    • 67650213557 scopus 로고    scopus 로고
    • note
    • Interestingly, the substrates bearing a C1-I as well as a C1-H (vs 13) preferentially cyclized to the phenanthrene skeleton.
  • 62
    • 67650228713 scopus 로고    scopus 로고
    • note
    • 3, 67%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.