Synthesis and antimicrobial spectrum of FCE 22101 and its orally available ester FCE 22891

The most efficient routes for the synthesis of FCE 22101, a pencm antibiotic characterized by a carbamoyloxymethyl sidechain at C-2 identical to that of cefuroxime and cefotaxime, and of FCE 22891, its orally absorbed pro-drug, are described. On the basis of in-vitro antimicrobial profile and other...

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Veröffentlicht in:Journal of antimicrobial chemotherapy 1989, Vol.23 (suppl-C), p.1-6
Hauptverfasser: Franceschi, G., Perrone, E., Alpegiani, M., Bedeschi, A., Battistini, C., Zarini, F., Bruna, C. Della
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container_end_page 6
container_issue suppl-C
container_start_page 1
container_title Journal of antimicrobial chemotherapy
container_volume 23
creator Franceschi, G.
Perrone, E.
Alpegiani, M.
Bedeschi, A.
Battistini, C.
Zarini, F.
Bruna, C. Della
description The most efficient routes for the synthesis of FCE 22101, a pencm antibiotic characterized by a carbamoyloxymethyl sidechain at C-2 identical to that of cefuroxime and cefotaxime, and of FCE 22891, its orally absorbed pro-drug, are described. On the basis of in-vitro antimicrobial profile and other characteristics the compounds have been considered worthy of further development.
doi_str_mv 10.1093/jac/23.suppl_C.1
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source Oxford University Press Journals Digital Archive legacy; MEDLINE
subjects Anti-Bacterial Agents - chemical synthesis
Anti-Bacterial Agents - pharmacology
Bacteria - drug effects
Carbapenems
Chemical Phenomena
Chemistry
Lactams
title Synthesis and antimicrobial spectrum of FCE 22101 and its orally available ester FCE 22891
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