Synthesis and antimicrobial properties of cephalosporin derivatives substituted on the C(7) nitrogen with arylmethyloxyimino or arylmethyloxyamino alkanoyl groups
D. Gentili et al., Synthesis and antimicrobial properties of cephalosporin derivatives substituted on the C(7) nitrogen with arylmethyloxyimino or arylmethyloxyamino alkanoyl groups, FARMACO, 54(4), 1999, pp. 224-231
Some 7-aminocephalosporanic acid (7-ACA) derivatives substituted on the C(7
) nitrogen with 2-(arylmethyloxyimino)propionyl (3a-f), 2-(arylmethyloxyami
no)propionyl (4a-d) and (arylmethyloxyamino)acetyl (2a-d) moieties were syn
thesized by reaction of the appropriate acylating agents with 7-ACA protect
ed as a t-butyl ester, followed by removal of the t-butyl protecting group.
The new compounds; tested in vitro for their antimicrobial activity agains
t Gram-positive and Gram-negative bacteria, proved to possess a modest acti
vity directed only against Gram-positive microorganisms. (C) 1999 Elsevier
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