Structure and stereochemistry of antibiotic PS-5.
- 1 January 1980
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 33 (8), 796-803
- https://doi.org/10.7164/antibiotics.33.796
Abstract
The structure and stereochemistry of a new β-lactam antibiotic PS-5were determined as shown in Fig. 3.This publication has 12 references indexed in Scilit:
- Thienamycin, a new .BETA.-lactam antibiotic. I. Discovery, taxonomy, isolation and physical properties.The Journal of Antibiotics, 1979
- Olivanic acids, a family of .BETA.-lactam antibiotics with .BETA.-lactamase inhibitory properties produced by Streptomyces species. I. Detection, properties and fermentation studies.The Journal of Antibiotics, 1979
- PS-5, a new .BETA.-lactam antibiotic. II. Antimicrobial activity.The Journal of Antibiotics, 1979
- PS-5, a new .BETA.-lactam antibiotic. I. Taxonomy of the producing organism, isolation and physico-chemical properties.The Journal of Antibiotics, 1979
- The penems, a new class of .beta.-lactam antibiotics: 6-acylaminopenem-3-carboxylic acidsJournal of the American Chemical Society, 1978
- Structure and absolute configuration of thienamycinJournal of the American Chemical Society, 1978
- In Vitro Activity of ThienamycinAntimicrobial Agents and Chemotherapy, 1978
- PS-5, A new .BETA.-lactam antibiotic from Streptomyces.The Journal of Antibiotics, 1977
- Aldol condensations of regiospecific penicillanate and cephalosporanate enolates. Hydroxyethylation at C-6 and C-7The Journal of Organic Chemistry, 1977
- Structure elucidation of MM 17880, a new fused β-lactam antibiotic isolated from Streptomyces olivaceus; a mild β-lactam degradation reactionJournal of the Chemical Society, Chemical Communications, 1977