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Volumn 20, Issue 12, 2010, Pages 3831-3833

Syntheses and biological evaluation of ring-C modified colchicine analogs

Author keywords

2 Nitrosopyridine; Colchicine; Cytotoxicity; Microtubule; Nitroso Diels Alder

Indexed keywords

COLCHICINE; COLCHICINE DERIVATIVE; ISOCOLCHICINE; TUBULIN;

EID: 77954212976     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2010.03.056     Document Type: Article
Times cited : (32)

References (14)
  • 8
    • 0000001557 scopus 로고
    • For a review of cycloaddition reactions of 2-methoxytropone, see: F. Pietra Chem. Rev. 73 1973 293
    • (1973) Chem. Rev. , vol.73 , pp. 293
    • Pietra, F.1
  • 11
    • 77954217329 scopus 로고    scopus 로고
    • The stereochemistry of 6a was conclusively determined by X-ray crystallographic analysis. See Ref. 6
    • The stereochemistry of 6a was conclusively determined by X-ray crystallographic analysis. See Ref. 6.
  • 12
    • 0000967997 scopus 로고
    • 2-Nitrosopyridine derivatives were synthesized in a two-step sequence (N,N-dimethyl sulfilimine intermediate formation, followed by oxidation using m-CPBA), see: E.C. Taylor, C.P. Tseng, and J.B. Rampal J. Org. Chem. 47 1982 552
    • (1982) J. Org. Chem. , vol.47 , pp. 552
    • Taylor, E.C.1    Tseng, C.P.2    Rampal, J.B.3
  • 13
    • 77954213737 scopus 로고    scopus 로고
    • note
    • 13C NMR patterns. For example, all the chemical shifts of the C-12 of the major isomers 6a-k are near 82.0 ppm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.