Works about OXAZOLIDINONES
Results: 299
Perfluoroalkyl‐Decorated Noble‐Metal‐Free MOFs for the Highly Efficient One‐Pot Four‐Component Coupling between Aldehydes, Amines, Alkynes, and Flue Gas CO<sub>2</sub>.
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- Angewandte Chemie, 2024, v. 136, n. 6, p. 1, doi. 10.1002/ange.202318115
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- Article
Thermocatalytic Conversion of CO<sub>2</sub> to Valuable Products Activated by Noble‐Metal‐Free Metal‐Organic Frameworks.
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- Angewandte Chemie, 2023, v. 135, n. 34, p. 1, doi. 10.1002/ange.202305213
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Reactivity of Glutaconamides Within [2]Rotaxanes: Mechanical Bond Controlled Chemoselective Synthesis of Highly Reactive α‐Ketoamides and their Light‐Triggered Cyclization.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202302681
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Highly Efficient Conversion of Propargylic Alcohols and Propargylic Amines with CO<sub>2</sub> Activated by Noble‐Metal‐Free Catalyst Cu<sub>2</sub>O@ZIF‐8.
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- Angewandte Chemie, 2022, v. 134, n. 19, p. 1, doi. 10.1002/ange.202114817
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Selectively Regulating Lewis Acid–Base Sites in Metal–Organic Frameworks for Achieving Turn‐On/Off of the Catalytic Activity in Different CO<sub>2</sub> Reactions.
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- Angewandte Chemie, 2022, v. 134, n. 18, p. 1, doi. 10.1002/ange.202200123
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Coupling of Cu(100) and (110) Facets Promotes Carbon Dioxide Conversion to Hydrocarbons and Alcohols.
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- Angewandte Chemie, 2021, v. 133, n. 9, p. 4929, doi. 10.1002/ange.202015159
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Palladium‐Catalyzed Regio‐, Diastereo‐, and Enantioselective 1,2‐Arylfluorination of Internal Enamides.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2731, doi. 10.1002/ange.202012882
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- Article
Polyurethanes from Direct Organocatalytic Copolymerization of p‐Tosyl Isocyanate with Epoxides.
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- Angewandte Chemie, 2021, v. 133, n. 3, p. 1617, doi. 10.1002/ange.202011902
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Kinetic Resolution of Tertiary 2‐Alkoxycarboxamido‐Substituted Allylic Alcohols by Chiral Phosphoric Acid Catalyzed Intramolecular Transesterification.
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- Angewandte Chemie, 2019, v. 131, n. 30, p. 10421, doi. 10.1002/ange.201905034
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Insight into the mechanochemistry of the Maillard reaction: degradation of Schiff bases via 5-oxazolidinone intermediate.
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- European Food Research & Technology, 2021, v. 247, n. 5, p. 1095, doi. 10.1007/s00217-021-03690-5
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- Article
IN VITRO EVALUATION OF THE EFFECTIVENESS OF DIFFERENT BODIPY DYES AS PHOTOSENSITIZER IN METHICILLIN-RESISTANT Staphylococcus aureus TREATMENT.
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- Mugla Journal of Science & Technology, 2018, v. 4, n. 2, p. 191, doi. 10.22531/muglajsci.448768
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Chemovariation and antibacterial activity of extracts and isolated compounds from species of Ixora and Greenea (Ixoroideae, Rubiaceae).
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6893
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- Article
Probing Nanoscale Interactions of Antimicrobial Zinc Oxide Quantum Dots on Bacterial and Fungal Cell Surfaces.
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- Advanced Materials Interfaces, 2022, v. 9, n. 3, p. 1, doi. 10.1002/admi.202101484
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A Graftable Quaternary Ammonium Biocidal Polymer Reduces Biofilm Formation and Ensures Biocompatibility of Medical Devices.
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- Advanced Materials Interfaces, 2021, v. 8, n. 5, p. 1, doi. 10.1002/admi.202001516
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Rational design of biodegradable sulphonamide candidates treating septicaemia by synergistic dual inhibition of COX-2/PGE2 axis and DHPS enzyme.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1737, doi. 10.1080/14756366.2022.2086868
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Synthesis and structure-activity relationships of novel 5-(hydroxamic acid)methyl oxazolidinone derivatives as 5-lipoxygenase inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 1471, doi. 10.1080/14756366.2020.1786082
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Quantum chemical modeling of the inhibition mechanism of monoamine oxidase by oxazolidinone and analogous heterocyclic compounds.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 1, p. 81, doi. 10.3109/14756366.2012.753882
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- Article
Determination of 3-Amino-2-oxazolidinone in Animal Tissue by an Enzyme-Linked Immunosorbent Assay and a Time-Resolved Fluoroimmunoassay.
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- Analytical Letters, 2015, v. 48, n. 8, p. 1275, doi. 10.1080/00032719.2014.979355
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Characterization of a Multiresistance Plasmid Carrying the optrA and cfr Resistance Genes From an Enterococcus faecium Clinical Isolate.
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- Frontiers in Microbiology, 2018, p. N.PAG, doi. 10.3389/fmicb.2018.02189
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Antibiotics Affect ROS Production and Fibroblast Migration in an In-vitro Model of Sinonasal Wound Healing.
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- Frontiers in Cellular & Infection Microbiology, 2020, p. 1, doi. 10.3389/fcimb.2020.00110
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ESTIMATION OF FORM-II CONTENT BY X-RAY DIFFRACTION IN LINEZOLID FILM COATED TABLETS.
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- Pharma Science Monitor, 2017, v. 8, n. 3, p. 38
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Antimicrobial stewardship and oxazolidinones use, a consideration for a Zambian health system.
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- Medical Journal of Zambia, 2019, v. 46, n. 3, p. 165, doi. 10.55320/mjz.46.3.553
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Source identification and entry pathways of banned antibiotics nitrofuran and chloramphenicol in shrimp value chain of Bangladesh.
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- EurAsian Journal of Biosciences, 2014, n. 8, p. 71, doi. 10.5053/ejobios.2014.8.0.7
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Diasteroselective conjugate addition of diethylaluminum cyanide to a conjugated N-enoyl system: an alternative synthesis of ( S)-pregabalin.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 1, p. 45, doi. 10.1139/cjc-2013-0397
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Testing of Medical Tablets Produced With Microcrystalline Cellulose Prepared From Agricultural Wastes.
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- Polymer Composites, 2014, v. 35, n. 7, p. 1343, doi. 10.1002/pc.22786
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Stereoselective synthesis of (−)‐cytoxazone and its unnatural congener (+)‐5‐epi‐cytoxazone.
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- Chirality, 2021, v. 33, n. 8, p. 479, doi. 10.1002/chir.23334
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A scalable synthesis of (+)‐coronafacic acid.
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- Chirality, 2020, v. 32, n. 4, p. 423, doi. 10.1002/chir.23172
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Genome-Wide Expression Profiling of the Response to Linezolid in Mycobacterium tuberculosis.
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- Current Microbiology, 2012, v. 64, n. 6, p. 530, doi. 10.1007/s00284-012-0104-9
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Development of novel antibacterial drugs to combat multiple resistant organisms.
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- Langenbeck's Archives of Surgery, 2015, v. 400, n. 2, p. 153, doi. 10.1007/s00423-015-1280-4
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Novel and highly efficient transformation of carbon dioxide into 2-oxazolidinones over Al-MCM-41 mesoporous-supported ionic liquids.
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- Environmental Technology, 2024, v. 45, n. 9, p. 1855, doi. 10.1080/09593330.2022.2156816
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Analysis of combined resistance to oxazolidinones and phenicols among bacteria from dogs fed with raw meat/vegetables and the respective food items.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-51918-y
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Synthesis, Antibacterial, Antioxidant, and Molecular Modeling Studies of Novel [2,3′-Biquinoline]-4-Carboxylic Acid and Quinoline-3-Carbaldehyde Analogs.
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- Journal of Chemistry, 2021, p. 1, doi. 10.1155/2021/9939506
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Synthesis, Molecular Docking, MEP and SAR Analysis, ADME-Tox Predictions, and Antimicrobial Evaluation of Novel Mono- and Tetra-Alkylated Pyrazole and Triazole Ligands.
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- Journal of Chemistry, 2021, p. 1, doi. 10.1155/2021/6663245
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Chitosan-S-triazinyl-bis(2-aminomethylpyridine) and Chitosan-S-triazinyl-bis(8-oxyquinoline) Derivatives: New Reagents for Silver Nanoparticle Preparation and Their Effect of Antimicrobial Evaluation.
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- Journal of Chemistry, 2020, p. 1, doi. 10.1155/2020/9590120
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Streptomyces sp. MNP32, a forest-dwelling Actinomycetia endowed with potent antibacterial metabolites.
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- 3 Biotech, 2023, v. 13, n. 7, p. 1, doi. 10.1007/s13205-023-03670-4
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Novel alginate/activated-charcoal platform for local treatment of resistant pathogens in wounds.
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- Chemical Industry / Hemijska Industrija, 2024, v. 78, p. 62
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Catalytic transformation of carbon dioxide into seven-membered heterocycles and their domino transformation into bicyclic oxazolidinones.
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- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-56681-5
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STUDIES ON POST HETEROCYCLIZATION OF 1, 3, 4-OXADIAZOLE CONTAINING AZETIDINONES DERIVATIVES AND THEIR BIOLOGICAL STUDIES.
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- Rasayan Journal of Chemistry, 2019, v. 12, n. 3, p. 1229, doi. 10.31788/RJC.2019.1235033
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Current Updates on Oxazolidinone and Its Significance.
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- International Journal of Medicinal Chemistry, 2012, p. 1, doi. 10.1155/2012/159285
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Cationic Conjugated Oligomers for Efficient and Rapid Antibacterial Photodynamic Therapy via Both Type I and Type II Pathways.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 1, p. 61, doi. 10.1002/cjoc.202300447
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Synthesis and Structure‐Activity Relationships of Ring‐Opened Bengamide Analogues against Methicillin‐ResistantStaphylococcus aureus<sup>†</sup>.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 3, p. 671, doi. 10.1002/cjoc.202000502
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Effects of Boiling on Nitrofuran AOZ Residues in Commercial Eggs.
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- Kafkas Universitesi Veteriner Fakultesi Dergisi, 2013, v. 19, n. 6, p. 1023, doi. 10.9775/kvfd.2013.9362
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A New Indole Glucoside and Other Constituents from the Sea Cucumber-Derived Aspergillus fumigatus M580 and Their Biological Activities.
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- Records of Natural Products, 2022, v. 16, n. 6, p. 633, doi. 10.25135/rnp.310.2110.2248
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A new 4-oxazolidinone from Sorghum halepense (L.) Pers.
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- Records of Natural Products, 2015, v. 9, n. 2, p. 247
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Synthesis, cytotoxicity and in vitro antibacterial screening of novel hydrazones bearing thienopyridine moiety as potent COX-2 inhibitors.
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- Journal of the Iranian Chemical Society, 2020, v. 17, n. 12, p. 3299, doi. 10.1007/s13738-020-01987-y
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Transition metal-catalyzed intramolecular cyclization of N-Boc-protected propargyl/ethynyl amines: a novel and convenient access to 2-oxazolidinone/oxazolone derivatives.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 3, p. 617, doi. 10.1007/s13738-018-1542-5
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Improving the toughness of polycyanate ester by adding epoxy pre‐polymer with different molecular weights.
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- Journal of Applied Polymer Science, 2020, v. 137, n. 45, p. 1, doi. 10.1002/app.49395
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Antioxidant, antibacterial, and antileishmanial potential of Micromeria nervosa extracts and molecular mechanism of action of the bioactive compound.
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- Journal of Applied Microbiology, 2023, v. 134, n. 2, p. 1, doi. 10.1093/jambio/lxad007
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Green synthesis of Ag doped ZnO nanoparticles: study of their structural, optical, thermal and antibacterial properties.
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- Materials Technology, 2022, v. 37, n. 13, p. 2785, doi. 10.1080/10667857.2022.2075307
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Early Experience with Tedizolid: Clinical Efficacy, Pharmacodynamics, and Resistance.
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- Pharmacotherapy, 2014, v. 34, n. 11, p. 1198, doi. 10.1002/phar.1491
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