Synthesis and antimicrobial properties of cephalosporin derivatives substituted on the C(7) nitrogen with arylmethyloxyimino or arylmethyloxyamino alkanoyl groups

Citation
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
Citations number
21
Categorie Soggetti
Pharmacology & Toxicology
Journal title
FARMACO
ISSN journal
0014827X → ACNP
Volume
54
Issue
4
Year of publication
1999
Pages
224 - 231
Database
ISI
SICI code
0014-827X(19990430)54:4<224:SAAPOC>2.0.ZU;2-P
Abstract
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 Science S.A. All rights reserved.