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Volumn 45, Issue 39, 2004, Pages 7255-7259

Access to enantiopure polycyclic β-lactams by Diels-Alder reaction of novel inner-outer-ring 2-(silyloxy)dienes with a carbacepham skeleton

Author keywords

Lactam; 2 Azetidinone; Carbacepham; Diels Alder cycloaddition; Diene

Indexed keywords

BETA LACTAM ANTIBIOTIC; CARBACEPHEM DERIVATIVE;

EID: 4444268853     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.022     Document Type: Article
Times cited : (13)

References (45)
  • 28
    • 0036214613 scopus 로고    scopus 로고
    • For a recent review on bi- and tricyclic-Î-lactams with nonclassical structure, see: B. Alcaide, and P. Almendros Curr. Org. Chem. 6 2002 245
    • (2002) Curr. Org. Chem. , vol.6 , pp. 245
    • Alcaide, B.1    Almendros, P.2
  • 29
    • 0000048258 scopus 로고
    • Intermolecular Diels-Alder Reactions
    • B.M. Trost I. Fleming Pergamon Oxford
    • W. Oppolzer Intermolecular Diels-Alder Reactions B.M. Trost I. Fleming Comprehensive Organic Synthesis Vol. 5 1991 Pergamon Oxford p 315
    • (1991) Comprehensive Organic Synthesis , vol.5
    • Oppolzer, W.1
  • 37
    • 0004030275 scopus 로고
    • M.I. Page Chapman and Hall London
    • Carbacephems are a promising new family of β-lactam antibiotics closely related to the widely used cephalosporins, with similar antibacterial profiles but with greater chemical stability and enhanced pharmacokinetic properties. See, for example: R.D.G. Cooper M.I. Page The Chemistry of β-Lactams 1992 Chapman and Hall London 272 Chapter 8
    • (1992) The Chemistry of β-Lactams , pp. 272
    • Cooper, R.D.G.1
  • 45
    • 4444260791 scopus 로고    scopus 로고
    • note
    • +-57, 11), 73 (100)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.