Results 161 to 170 of about 6,381 (215)
Antimicrobial Resistance of ESKAPE Pathogens Identified in Patients with Necrotizing Fasciitis: A 10-Year Retrospective Study. [PDF]
Radu-Adameşteanu MO +7 more
europepmc +1 more source
Studies of 2-Oxazolidinones. (II) : Products of the Pyrolysis of Some 2-Oxazolidinones
openaire
Drug monitoring and individual dose optimization of antimicrobial drugs: oxazolidinones
INTRODUCTION: Oxazolidinones are synthetic antibiotics with bacteriostatic activity against Gram-positive pathogens. Linezolid, the first marketed oxazolidinone, has shown also activity against Mycobaterium tuberculosis, including multidrug-resistant and
Dario Cattaneo, , Michael Neely
exaly +2 more sources
A novel way to chiral 2-oxazolidinones: selenium-catalyzed cyclocarbonylation of 2-aminoethanols
Selenium-catalyzed cyclocarbonylation of 2-aminoethanols with CO under atmospheric pressure at 30 degrees C afforded 2-oxazolidinones in excellent yields without any other co-catalyst.
Shiwei Lu
exaly +2 more sources
Synthesis of oxazolidinones in supercritical CO2 under heterogeneous catalysis [PDF]
Basic alumina efficiently promotes the reaction of propargylamines with scCO2 for the synthesis of variously substituted oxazolidinones that, after catalyst filtration, are easily isolated by methanol ...
Raimondo Maggi, Maurizio Selva
exaly +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Drugs, 2000
The oxazolidinones represent a novel chemical class of synthetic antimicrobial agents. They exhibit an unique mechanism of protein synthesis inhibition and generally display bacteriostatic activity against many important human pathogens, including methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci, and penicillin- and ...
D I, Diekema, R N, Jones
openaire +2 more sources
The oxazolidinones represent a novel chemical class of synthetic antimicrobial agents. They exhibit an unique mechanism of protein synthesis inhibition and generally display bacteriostatic activity against many important human pathogens, including methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci, and penicillin- and ...
D I, Diekema, R N, Jones
openaire +2 more sources
The Lancet, 2001
Many common gram-positive pathogens (eg, Staphylococcus aureus, Enterococcus spp, and Streptococcus pneumoniae) have become increasingly resistant to antimicrobial agents, and new drugs with activity against gram-positive bacteria are urgently needed. The oxazolidinones, a new chemical class of synthetic antimicrobial agent, have a unique mechanism of ...
D J, Diekema, R N, Jones
openaire +2 more sources
Many common gram-positive pathogens (eg, Staphylococcus aureus, Enterococcus spp, and Streptococcus pneumoniae) have become increasingly resistant to antimicrobial agents, and new drugs with activity against gram-positive bacteria are urgently needed. The oxazolidinones, a new chemical class of synthetic antimicrobial agent, have a unique mechanism of ...
D J, Diekema, R N, Jones
openaire +2 more sources
Oxazolidinones as novel human CCR8 antagonists
High-throughput screening of the corporate compound collection led to the discovery of a novel series of N-substituted-5-aryl-oxazolidinones as potent human CCR8 antagonists. The synthesis, structure-activity relationships, and optimization of the series
David P Andrew +2 more
exaly +2 more sources
Acta Crystallographica Section C Crystal Structure Communications, 1997
Redetermination of the crystal structure of the title compound, C3H5NO2, leads to a precise geometry for this molecule that is compared with the conformation of several aryl-substituted oxazolidinones. Molecular cohesion is stabilized by hydrogen bonds between the amine and carbonyl groups.
Wouters, Johan +2 more
openaire +2 more sources
Redetermination of the crystal structure of the title compound, C3H5NO2, leads to a precise geometry for this molecule that is compared with the conformation of several aryl-substituted oxazolidinones. Molecular cohesion is stabilized by hydrogen bonds between the amine and carbonyl groups.
Wouters, Johan +2 more
openaire +2 more sources

