Synthesis and Reactivity with β-Lactamases of “Penicillin-like” Cyclic Depsipeptides-Reference-Cited by-同舟云学术

Synthesis and Reactivity with β-Lactamases of “Penicillin-like” Cyclic Depsipeptides

Published:1999-01-09 Issue:3 Volume:64 Page:713-720
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cabaret D.¹,Adediran S. A.¹,Garcia Gonzalez M. J.¹,Pratt R. F.¹,Wakselman M.¹

Affiliation:

1. SIRCOB, Université de Versailles - Saint Quentin-en-Yvelines, Bâtiment Lavoisier, 45 Avenue des Etats Unis, F-7800, Versailles, France, and Department of Chemistry, Wesleyan University, Middletown, Connecticut 06459

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980564%2B

Reference53 articles.

1. Neuhaus, F. C.; Georgopapadakou, N. H. InEmergingTargetsinAntibacterialandAntifungalChemotherapy; Sutcliffe, J., Georgopapadakou, N. H., Eds.; Routledge, Chapman & Hall: New York, 1992; pp 205−273.

2. Evolution and Dissemination of β-Lactamases Accelerated by Generations of β-Lactam Antibiotics

3. beta-Lactamase-catalyzed hydrolysis of acyclic depsipeptides and acyl transfer to specific amino acid acceptors.

4. Kinetics and mechanism of the serine .beta.-lactamase catalyzed hydrolysis of depsipeptides

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