Desulphurative approaches to penem antibiotics. IV. Bromination of 3-methyl-2-thiacephems, a novel entry in the synthesis of potent antimicrobial agents-Reference-Cited by-同舟云学术

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Desulphurative approaches to penem antibiotics. IV. Bromination of 3-methyl-2-thiacephems, a novel entry in the synthesis of potent antimicrobial agents

Published:1983-01 Issue:31 Volume:24 Page:3283-3286
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Perrone Ettore,Alpegiani Marco,Bedeschi Angelo,Giudici Franco,Foglio Maurizio,Franceschi Giovanni

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Choice of chemotherapy for infection by Staphylococcus aureus

2. 2-(Alkylthio)penem-3-carboxylic acids. V. Synthesis and antibacterial activities of "1-thiathienamycin" and related compounds.

3. Biological activity of (5R,6S,8R)-6-.ALPHA.-hydroxyethyl-2-acetoxymethyl-2-penem-3-carboxylate.

4. 2-(Alkylthio)penem-3-carboxylic acids II. Chemical manipulation of penem side chains.

5. Penems. I. Novel synthesis of antibacterial penem compounds utilizing 1,3-dithiolane derivatives

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1. Trichloroacetyl Isocyanate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

2. Tetrabutylammonium Acetate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

3. Synthesis of γ-and δ-lactones derived from 4-quinolone-3-carboxylic acid;Tetrahedron Letters;1997-02

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

5. Other Fused Azetidines, Azetines, and Azetes;Comprehensive Heterocyclic Chemistry II;1996

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