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Volumn 50, Issue 37, 2011, Pages 8474-8477

Isoxazole functionalization technologies enable construction of tetracycline derivatives

Author keywords

antimicrobial agents; bacterial resistance; isoxazole; seragakinone A; tetracycline

Indexed keywords

ANTI-MICROBIAL AGENT; BACTERIAL RESISTANCE; ISOXAZOLES; SERAGAKINONE A; TETRACYCLINE;

EID: 80052442221     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201102480     Document Type: Article
Times cited : (32)

References (28)
  • 5
    • 79251631666 scopus 로고    scopus 로고
    • For a recent discussion of mechanism(s) of action leading to non-antimicrobial properties of tetracycline compounds
    • For a recent discussion of mechanism(s) of action leading to non-antimicrobial properties of tetracycline compounds, see:, M. O. Griffin, G. Ceballos, F. J. Villarreal, Pharm. Res. 2011, 63, 102-107.
    • (2011) Pharm. Res. , vol.63 , pp. 102-107
    • Griffin, M.O.1    Ceballos, G.2    Villarreal, F.J.3
  • 7
    • 0034704217 scopus 로고    scopus 로고
    • For a structural explanation for the antibiotic action of tetracycline on the 30S ribosomal subunit
    • For a structural explanation for the antibiotic action of tetracycline on the 30S ribosomal subunit, see:, D. E. Brodersen, W. M. Clemons, Jr., A. P. Carter, R. J. Morgan-Warren, B. T. Wimberly, V. Ramakrishnan, Cell 2000, 103, 1143-1154.
    • (2000) Cell , vol.103 , pp. 1143-1154
    • Brodersen, D.E.1    Clemons Jr., W.M.2    Carter, A.P.3    Morgan-Warren, R.J.4    Wimberly, B.T.5    Ramakrishnan, V.6
  • 22
    • 34250899206 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3252-3254.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 3252-3254
  • 25
    • 79952055800 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 2297-2301.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 2297-2301
  • 27
    • 80052455299 scopus 로고    scopus 로고
    • For a recently reported one-pot synthesis of 3-substituted isoxazole-4-carbaldehydes
    • For a recently reported one-pot synthesis of 3-substituted isoxazole-4-carbaldehydes, see:, J. A. Burkhard, B. H. Tchitchanov, E. M. Carreira, Angew. Chem. 2011, 123, 5491-5495
    • (2011) Angew. Chem. , vol.123 , pp. 5491-5495
    • Burkhard, J.A.1    Tchitchanov, B.H.2    Carreira, E.M.3
  • 28
    • 79957479241 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 5379- 5382.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5379-5382


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.