Issue 0, 1983

New polycyclic β-lactams. Synthesis of 2a,3-dihydroazeto[1,2-a]quinoline-1,4(2H)-diones, structural analogues of the carbacephalosporin antibiotics

Abstract

A method has been developed for the preparation of dihydroxydihydroazeto[1,2-a]quinoline-1,4(2H)-diones (1). The synthesis involved, as a key step, the completion of the polycyclic β-lactam system by a modified Bischler–Napieralski reaction. It was illustrated by the synthesis of (±)-7,8-dihydroxy-3,3-dimethyl-2-phenoxyacetamido-2a,3-dihydroazeto[1,2-a]quinoline-1,4(2H)-dione (20), which is structurally related to the carbacephalosporin antibiotics.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1983, 1925-1928

New polycyclic β-lactams. Synthesis of 2a,3-dihydroazeto[1,2-a]quinoline-1,4(2H)-diones, structural analogues of the carbacephalosporin antibiotics

M. D. Bachi and J. Klein, J. Chem. Soc., Perkin Trans. 1, 1983, 1925 DOI: 10.1039/P19830001925

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