Issue 0, 1973

Synthetic studies related to nuclear analogues of the penicillins and cephalosporins

Abstract

A route developed for the synthesis of nuclear analogues of the penicillins and cephalosporins has been used to generate 2,2-dimethyl-8-oxo-7β-phenylacetamido-4-thia-1-aza-6αH-bicyclo[4·2·0]octane-3-carboxylic acid (17; R = H).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1973, 479-484

Synthetic studies related to nuclear analogues of the penicillins and cephalosporins

G. Lowe and M. V. J. Ramsay, J. Chem. Soc., Perkin Trans. 1, 1973, 479 DOI: 10.1039/P19730000479

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