Synthesis and activity of cephalosporins containing an oxyiminomethylene functionality in the ortho-position of a phenyl- or phenoxyacetic acid C-7 side chain substituent
Articolo
Data di Pubblicazione:
1998
Citazione:
Synthesis and activity of cephalosporins containing an oxyiminomethylene functionality in the ortho-position of a phenyl- or phenoxyacetic acid C-7 side chain substituent / D. Albanese, D. Landini, M. Leone, M. Penso, M. Zenoni. - In: IL FARMACO. - ISSN 0014-827X. - 53:10-11(1998), pp. 709-717.
Abstract:
A new series of cephalosporins having in the C-7 side chain a phenyl- or a phenoxyacetamido group bearing an oxyiminomethyl function in the ortho-position of the aromatic ring was prepared. Their in vitro activity was tested against both Gram+ and Gram- strains. (C) 1998 Elsevier Science S.A. All rights reserved.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
β-lactam antibiotics; Oxyacetamido cephalosporins; Oxyiminomethylene cephalosporins; Phase transfer catalysis
Elenco autori:
D. Albanese, D. Landini, M. Leone, M. Penso, M. Zenoni
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