𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Sulfazecin and isosulfazecin, novel β-lactam antibiotics of bacterial origin

✍ Scribed by Imada, A.; Kitano, K.; Kintaka, K.; Muroi, M.; Asai, M.

Book ID
109721990
Publisher
Nature Publishing Group
Year
1981
Tongue
English
Weight
324 KB
Volume
289
Category
Article
ISSN
0028-0836

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Theoretical studies on β-lactam antibiot
Theoretical studies on β-lactam antibiotics. IV. Conformational analysis of novel β-lactam antibiotics and the binding specificities of crosslinking enzyme(s) and β-lactamases
✍ T. K. Vasudevan; V. S. R. Rao 📂 Article 📅 1981 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 609 KB

## Abstract Conformational‐energy calculations were carried out on the new family of β‐lactam antibiotics (viz., thienamycin, PS‐5, 1‐oxa‐ and 1‐thiapenems, and their close analogs); these exhibit broad‐spectrum antibacterial activity and stability towards β‐lactamase‐producing strains. The bicycli

ChemInform Abstract: Enzymatic Synthesis
ChemInform Abstract: Enzymatic Synthesis and Activity of Novel β-Lactam Antibiotics. Part 3. Novel β-Lactam Antibiotics Synthesized by Amination of Catechols Using Fungal Laccase.
✍ Annett Mikolasch; Martina Wurster; Michael Lalk; Sabine Witt; Simone Seefeldt; E 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A Novel Approach to the Synthesis of Pre
A Novel Approach to the Synthesis of Precursors of Tricyclic β-Lactam Antibiotics
✍ Rita Annunziata; Maurizio Benaglia; Mauro Cinquini; Franco Cozzi; Laura Poletti; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 296 KB 👁 1 views

The stereoselective synthesis of two precursors of tricyclic β-ring-forming reaction followed by the reduction of a functionalized aromatic substituent at C-4 of the β-lactam lactam antibiotics (trinems) has been attempted by a novel approach that involves a highly stereoselective azetidinone nucleu