메뉴 건너뛰기




Volumn 62, Issue 43, 2006, Pages 10171-10181

Stereochemically pure α-trifluoromethyl-malic hydroxamates: synthesis and evaluation as inhibitors of matrix metalloproteinases

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TRIFLUOROMETHYL MALIC HYDROXAMATE DERIVATIVE; FLUORINE DERIVATIVE; GELATINASE A; GELATINASE B; HYDROXAMIC ACID; MALIC ACID DERIVATIVE; MATRIX METALLOPROTEINASE INHIBITOR; N ACYL OXAZOLIDINE 2 THIONE; OXAZOLIDINE DERIVATIVE; PYRUVIC ACID DERIVATIVE; TRIFLUOROPYRUVATE; UNCLASSIFIED DRUG;

EID: 33748437500     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.08.036     Document Type: Article
Times cited : (9)

References (37)
  • 1
    • 0003518240 scopus 로고    scopus 로고
    • Ojima I., McCarthy J.R., and Welch J.T. (Eds), ACS Books; American Chemical Society, Washington, DC
    • In: Ojima I., McCarthy J.R., and Welch J.T. (Eds). Biomedical Frontiers of Fluorine Chemistry (1996), ACS Books; American Chemical Society, Washington, DC
    • (1996) Biomedical Frontiers of Fluorine Chemistry
  • 10
    • 33748433593 scopus 로고    scopus 로고
    • note
    • 2.
  • 12
  • 19
    • 33748413696 scopus 로고    scopus 로고
    • note
    • CCDC 601635 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033; e-mail: deposi@ccdc.cam.ac.uk).
  • 20
  • 22
    • 85004882387 scopus 로고
    • 2 undergoes rapid decomposition even at 4 °C, therefore it must be used within 1-2 h from its preparation. Our results are in agreement with an earlier report:
    • 2 undergoes rapid decomposition even at 4 °C, therefore it must be used within 1-2 h from its preparation. Our results are in agreement with an earlier report:
    • (1978) Synthesis , pp. 474-476
    • Gorecka, A.1    Leplawy, M.2    Zabrocki, J.3    Zwierzak, A.4
  • 24
    • 0037178970 scopus 로고    scopus 로고
    • For the addition of amine nucleophiles to β-lactones see:
    • For the addition of amine nucleophiles to β-lactones see:. Nelson S.G., Spencer K.L., Cheung W.S., and Mamie S.J. Tetrahedron 58 (2002) 7081-7091
    • (2002) Tetrahedron , vol.58 , pp. 7081-7091
    • Nelson, S.G.1    Spencer, K.L.2    Cheung, W.S.3    Mamie, S.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.