A synthesis of 4-carboxy-3-methylceph-3-em 1,1-dioxide involving a new strategy for the ring enlargement of penicillanate 1,1-dioxides-Reference-Cited by-同舟云学术

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A synthesis of 4-carboxy-3-methylceph-3-em 1,1-dioxide involving a new strategy for the ring enlargement of penicillanate 1,1-dioxides

Published:1985-01 Issue:4 Volume:26 Page:497-500
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sriyani Ananda G.D.,Stoodley Richard J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Clavulanic acid, a novel β-lactam isolated from Streptomyces clavuligerus; X-ray crystal structure analysis

2. CP-45,899, a Beta-Lactamase Inhibitor That Extends the Antibacterial Spectrum of Beta-Lactams: Initial Bacteriological Characterization

3. Chemical studies on the inactivation of Escherichia coli RTEM β-lactamase by clavulanic acid

4. Inactivation of radiolabeled RTEM .beta.-lactamase from Escherichia coli by clavulanic acid and 9-deoxyclavulanic acid

5. The inhibition of staphylococcal β-lactamase by clavulanic acid

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1. Sodium 2-Ethylhexanoate;Encyclopedia of Reagents for Organic Synthesis;2016-03-31

2. 4-Oxoazetidine-2-sulfinic Acid and Its Derivatives;Sulfur reports;1996-05

3. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996

4. Cephalosporins;Comprehensive Heterocyclic Chemistry II;1996

5. Synthesis of a highly reactive 1,1-dicyanomethylene-1-dethiacephalosporin;Tetrahedron Letters;1992-10

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