메뉴 건너뛰기




Volumn 45, Issue 2, 2005, Pages 285-290

Ferrocene-mediated proton-coupled electron transfer in a series of ferrocifen-type breast-cancer drug candidates

Author keywords

Antitumor agents; Electrochemistry; Electron transfer; Hormones; Metallocenes

Indexed keywords

CELLS; DRUG PRODUCTS; ELECTROCHEMISTRY; HORMONES; PROTONS; TUMORS;

EID: 29544436942     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200502925     Document Type: Article
Times cited : (381)

References (37)
  • 2
    • 0037435046 scopus 로고    scopus 로고
    • b) for recent reviews on the biological mechanisms of SERMs, see: V. C. Jordan, J. Med. Chem. 2003, 46, 883
    • (2003) J. Med. Chem. , vol.46 , pp. 883
    • Jordan, V.C.1
  • 11
    • 29544447947 scopus 로고    scopus 로고
    • note
    • Herein, Cytotoxicity is defined as an antiproliferative effect that, in contrast to an antihormonal effect, is not reversed by the addition of estradiol.
  • 17
    • 29544438808 scopus 로고    scopus 로고
    • note
    • + moiety.
  • 18
    • 29544438460 scopus 로고    scopus 로고
    • note
    • In our system, phenol oxidation waves occurred at potentials higher than 0.8 V vs. SCE.
  • 25
    • 29544441934 scopus 로고    scopus 로고
    • unpublished results
    • The involvement of a quinone methide species subsequent to the electron-transfer activation is further supported by the observation that the meio-OH-substituted analogues that have been tested did not show any reactivity following their initial one-electron oxidation in the presence of base (comparable to Figure 3 a), whereas intramolecular electron transfer was observed electrochemically when a para-phenol was added to the meta-substituted derivative, (comparable to Figure 3 b). (P. Pigeon, A. Vessières, E. Hillard, G. Jaouen, unpublished results).
    • Pigeon, P.1    Vessières, A.2    Hillard, E.3    Jaouen, G.4
  • 34
    • 29544441366 scopus 로고    scopus 로고
    • unpublished results
    • A. Vessières, E. A. Hillard, P. Pigeon, S. Top, K. Kowalski, J. Zakrzewski, G. Jaouen, unpublished results. Compounds 4, 7, and 8 were synthesized by McMurry cross-coupling reactions between 3- chloropropionylferrocene and 4,4′-dihydroxybenzophenone, ferrocene ethyl ketone and 4-hydroxy,4′-methoxybenzophenone, and 4-hydroxyphenylethyl ketone and 4-methoxyphenylferrocenyl ketone, respectively, and characterized by NMR spectroscopy and HRMS.
    • Vessières, A.1    Hillard, E.A.2    Pigeon, P.3    Top, S.4    Kowalski, K.5    Zakrzewski, J.6    Jaouen, G.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.