Results 11 to 20 of about 2,355 (106)

Antimicrobial Effect of Oxazolidinones and Its Synergistic Effect with Bedaquiline Against Mycobacterium abscessus Complex

open access: yesInfection and Drug Resistance, 2023
Tianhui Gao,1,* Cong Yao,1,* Yuanyuan Shang,1 Renchun Su,1 Xuxia Zhang,1 Weicong Ren,1 Shanshan Li,1 Wei Shu,2 Yu Pang,1 Qi Li2 1Department of Bacteriology and Immunology, Beijing Key Laboratory for Drug-Resistant Tuberculosis Research, Beijing ...
Gao T   +9 more
doaj   +1 more source

New Oxazolidinones for Tuberculosis: Are Novel Treatments on the Horizon?

open access: yesPharmaceutics
Multidrug-resistant tuberculosis (MDR-TB) is a global health concern. Standard treatment involves the use of linezolid, a repurposed oxazolidinone. It is associated with severe adverse effects, including myelosuppression and mitochondrial toxicity.
Ricky Hao Chen   +4 more
doaj   +3 more sources

A Critical Review of Oxazolidinones: An Alternative or Replacement for Glycopeptides and Streptogramins? [PDF]

open access: yesCanadian Journal of Infectious Diseases, 2001
OBJECTIVE: To review the available data on the oxazolidinones linezolid and eperezolid.
George G Zhanel   +5 more
doaj   +2 more sources

Palladium-catalyzed formation of oxazolidinones from biscarbamates: a mechanistic study [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2011
Oxazolidinones can be synthesized starting from cyclic biscarbamates via a palladium-catalyzed reaction. To test the proposed mechanism of this reaction, first, bicyclonorcarene endoperoxides derived from cyano and carbomethoxy cycloheptatrienes were ...
Benan Kilbas, Metin Balci
doaj   +2 more sources

Ligand-Free Ullmann-Type Arylation of Oxazolidinones by Diaryliodonium Salts [PDF]

open access: yes, 2022
The arylation of azaheterocycles can be considered as one of the most important processes for the preparation of various biologically active compounds.
Natalia , Soldatova   +7 more
core   +2 more sources

oxazolidinones

open access: yes, 2022
Archive of oxazolidinones containing sub-folders named after each compound and its net charge. Every compound's folder contains a total of 20 files distributed into three sub-directories reporting QM (QM/), FF (FF/), and MD (MD ...
Giuliano Malloci (2060875)   +5 more
core   +1 more source

N-Acylation of Oxazolidinones via Aerobic Oxidative NHC Catalysis [PDF]

open access: yes, 2018
In the ongoing quest to find alternatives to atom un-economical and forcing conditions in acylation reactions, aerobic oxidative NHC catalysis has emerged as a method to convert aldehydes to potent acylating reagents.
Henrik Sundén (1399444)   +15 more
core   +1 more source

Synthesis of oxazolidinones from N-aryl-carbamate and epichlorohydrin under mild conditions [PDF]

open access: yes, 2022
The reaction conditions for an enantiospecific synthesis of various N-aryl-oxazolidinones from N-aryl-carbamates and (R) or (S) epichlorohydrin were optimized.
Buscemi S.   +4 more
core   +1 more source

Synthesis of Oxazolidinones by a Hypervalent Iodine Mediated Cyclization of N‐Allylcarbamates [PDF]

open access: yes, 2021
The preparation of oxazolidinones by the hypervalent iodine mediated cyclization of allylcarbamates is described. A versatile range of substrates can be converted into substituted oxazolidinones primed for further transformations.
Lo, Pui Kin Tony   +8 more
core   +1 more source

Systems to Access 5‐Aryl‐2‐Oxazolidinones: Catalyst‐Free Synthesis Under Ambient Conditions [PDF]

open access: yes, 2020
The development of sustainable synthetic routes to access valuable oxazolidinones via CO2 fixation is an active research area, and the aziridine/carbon dioxide coupling has aroused a considerable interest. This reaction features a high activation barrier
Pampaloni G.   +17 more
core   +3 more sources

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