Isolation and characterization of side-products formed through ∆2-isomerization in the synthesis of cefpodoxime proxetil
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmacology
Link
http://www.nature.com/articles/s41429-019-0190-z.pdf
Reference17 articles.
1. Dabernat H, Avril JL, Boussougant Y. In-vitro activity of cefpodoxime against pathogens responsible for community-aquired respiratory tract infections. J Antimicrob Chemother. 1990;26E:1–6.
2. Fujimoto K, Ishihara S, Yanagisawa H, Ide J, Nakayama E, et al. Studies on orally active cephalosporin esters. J Antibiot. 1987;40:370–84.
3. Chocas EC, Paap CM, Godley PJ. Cefpodoxime proxetile: a new broad-spectrum, oral cephalosporin. Ann Pharmacother. 1993;27:1369–77.
4. Saathoff N, Lode H, Neider K, Depperman KM, Borner K, et al. Phamacokinetics of cefpodoxime proxetil and interactions with an antacid and an H2 receptor antagonist. AAC. 1992;36:796–800.
5. Fulton B, Perry CM. Cefpodoxime proxetile. Pediatr Drugs. 2001;3:137–58.
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