Semisynthetic cephalosporins. Synthesis and structure-activity relations of 7-mandelamido-3-cephem-4-carboxylic acids

…, LL Lam, JJ Taggart, JR Guarini, L Phillips

Index: Hoover; Dunn; Jakas; Lam; Taggart; Guarini; Phillips Journal of Medicinal Chemistry, 1974 , vol. 17, # 1 p. 34 - 41

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Citation Number: 36

Abstract

Most of the several cephalosporins that have been found to be clinically useful incorporate at the 7 position an acyl moiety derived from acetic acid, monosubstituted with an appropriate grouping such as thiophene, tetrazole. pyridylthio, or cyano. Structure-activity studies on cephalosporins teach that homologation or substitution of the acetic acid by a second grouping is generally undesirable from the standpoint of level and breadth of ...