Traceless Staudinger Ligation To Introduce Chemical Diversity on β-Lactamase Inhibitors of Second Generation
Author:
Affiliation:
1. Université de Paris, UMR CNRS 8601, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, F-75006 Paris, France
2. INSERM, Sorbonne Université, Université de Paris, Centre de Recherche des Cordeliers (CRC), F-75006 Paris, France
Funder
Agence Nationale de la Recherche
Association Vaincre la Mucoviscidose
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02741
Reference36 articles.
1. A resurgence of β-lactamase inhibitor combinations effective against multidrug-resistant Gram-negative pathogens
2. Avibactam is a covalent, reversible, non- -lactam -lactamase inhibitor
3. The road to avibactam: the first clinically useful non-β-lactam working somewhat like a β-lactam
4. Three Decades of β-Lactamase Inhibitors
5. Synthetic approaches towards avibactam and other diazabicyclooctane β-lactamase inhibitors
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1. Approachable Synthetic Methodologies for Second-Generation β-Lactamase Inhibitors: A Review;Pharmaceuticals;2024-08-23
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3. Synergistic Antibacterial Activity of Meropenem and Imipenem in Combination with Diazabicyclooctane Derivatives;Russian Journal of General Chemistry;2022-10
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