Volume 21, Issue 37
Natural Products
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ChemInform Abstract: Synthesis and Antimicrobial Properties of Substituted 3-Aminoxy-(E)-2-methoxyiminopropionyl Penicillins and Cephalosporins.

A. BALSAMO

A. BALSAMO

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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B. MACCHIA

B. MACCHIA

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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A. MARTINELLI

A. MARTINELLI

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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E. ORLANDINI

E. ORLANDINI

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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A. ROSSELLO

A. ROSSELLO

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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F. MACCHIA

F. MACCHIA

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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G. BROCALLI

G. BROCALLI

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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P. DOMIANO

P. DOMIANO

Ist. Chim. Farm., Univ. Pisa, 56100 Pisa, Italy

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First published: September 11, 1990

Abstract

The title compounds of type (IV), (V) and (VI) are synthesized as described in the scheme.

ChemInform Abstract

The title compounds of type (IV), (V) and (VI) are synthesized as described in the scheme. Comparison of (IVa), (Va) and (VIa) with their analogues which lack the methoxyimino group shows that the antimicrobial activity of the former is generally lower. Only in the case of (IVa) higher activity toward Gram-positive resistant germs is observed. (IV) are also more active than penicillin G toward Gram-positive β-lactamase-producing germs.

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