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Volumn 1, Issue 1, 2006, Pages 37-40

Structure-activity relationships in side-chain-modified epothilone analogues - How important is the position of the nitrogen atom?

Author keywords

Antitumor agents; Epothilones; Natural products; Structure activity relationships; Total synthesis

Indexed keywords

EPOTHILONE DERIVATIVE; NITROGEN;

EID: 33746306765     PISSN: 18607179     EISSN: 18607187     Source Type: Journal    
DOI: 10.1002/cmdc.200500051     Document Type: Article
Times cited : (26)

References (34)
  • 4
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    • Angew. Chem. Int. Ed. 2005, 44, 2838-2850;
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 2838-2850
  • 9
    • 0032541259 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 2014-2045.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2014-2045
  • 17
    • 0038339605 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 2511-2515.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2511-2515
  • 20
    • 33746270195 scopus 로고    scopus 로고
    • note
    • Epo D is the 12/13-deoxy derivative of Epo B; it incorporates a cis double bond between C12 and C13 in place of an epoxide moiety.
  • 24
    • 1842550988 scopus 로고
    • Compound 7 was prepared from the known 2,6-dimethyl-benzothiazole (M.J. Spitulnik, Synthesis 1976, 730-731) by light-catalyzed bromination with NBS (W lamp, 80 C, 4 h) and subsequent treatment of the brominated intermediate with AcOH and hexamethylene tetraamine (2 h, 36%).
    • (1976) Synthesis , pp. 730-731
    • Spitulnik, M.J.1
  • 29
    • 33746275572 scopus 로고    scopus 로고
    • note
    • 2 at 160 C) analogously to the synthesis of 6. Details of the synthesis of 14 will be published elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.