Works matching DE "OXAZOLIDINONES synthesis"
Results: 56
Protonated Porphyrins: Bifunctional Catalysts for the Metal‐Free Synthesis of N‐Alkyl‐Oxazolidinones.
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- Chemistry - A European Journal, 2023, v. 29, n. 1, p. 1, doi. 10.1002/chem.202202729
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Synthesis, screening and antimicrobial activity evaluation of spiro indolothiazolidinone, oxazolidinone and azetidene derivatives of benzenesulfonyl chloride.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 7, p. 429, doi. 10.1007/s11094-012-0814-0
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Comprehensive spectral identification of key intermediates to the final product of the chiral pool synthesis of radezolid.
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- Chemistry Central Journal, 2017, v. 11, p. 1, doi. 10.1186/s13065-017-0309-x
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Daily 300 mg dose of linezolid for multidrug-resistant and extensively drug-resistant tuberculosis: updated analysis of 51 patients.
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- Journal of Antimicrobial Chemotherapy (JAC), 2012, v. 67, n. 6, p. 1503, doi. 10.1093/jac/dks078
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Cooperative Catalysis of Ru(III)‐Porphyrin in CO<sub>2</sub>‐Involved Synthesis of Oxazolidinones.
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- Chemistry - An Asian Journal, 2021, v. 16, n. 17, p. 2504, doi. 10.1002/asia.202100533
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Non‐Reductive CO<sub>2</sub> Valorization into Oxazolidinones via Cycloaddition to Aziridines: A Personal Insight.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 39, p. 1, doi. 10.1002/ejoc.202400616
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Front Cover: Facile Multicomponent Synthesis of Oxazolidinones from Primary Amines and Cesium (Hydrogen)Carbonate (Eur. J. Org. Chem. 27/2023).
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- European Journal of Organic Chemistry, 2023, v. 26, n. 27, p. 1, doi. 10.1002/ejoc.202300636
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Facile Multicomponent Synthesis of Oxazolidinones from Primary Amines and Cesium (Hydrogen)Carbonate.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 27, p. 1, doi. 10.1002/ejoc.202300135
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Synthesis of oxazolidinones from N-aryl-carbamate and epichlorohydrin under mild conditions.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 140, doi. 10.24820/ark.5550190.p011.706
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An expeditious construction of 3-aryl-5-(substituted methyl)-2-oxazolidinones: a short and efficient synthesis of Linezolid.
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- ARKIVOC: Online Journal of Organic Chemistry, 2012, p. 45
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Cu<sub>x</sub>O<sub>y</sub> Incorporated COF: A Potential Reusable Catalyst for the Synthesis of α‐Hydroxy Ketones and Oxazolidinones Under Atmospheric CO<sub>2</sub> Pressure and Solvent‐Free Conditions.
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- ChemCatChem, 2024, v. 16, n. 22, p. 1, doi. 10.1002/cctc.202400920
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A Ni‐Based Metal‐Organic Framework with Polarizing Traits for Efficient Heterogeneous Catalysis in the Sustainable Synthesis of Oxazolidinones.
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- ChemCatChem, 2024, v. 16, n. 19, p. 1, doi. 10.1002/cctc.202400429
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Synthesis of Oxazolidinones and Derivatives through Three‐Component Fixation of Carbon Dioxide.
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- ChemCatChem, 2018, v. 10, n. 14, p. 3057, doi. 10.1002/cctc.201800142
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Conversion of Carbon Dioxide into Oxazolidinones Mediated by Quaternary Ammonium Salts and DBU.
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- ChemCatChem, 2017, v. 9, n. 24, p. 4451, doi. 10.1002/cctc.201700594
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Synthesis of Oxazolidinones from Epoxides and Isocyanates Catalysed by Aluminium Heteroscorpionate Complexes.
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- ChemCatChem, 2016, v. 8, n. 12, p. 2100, doi. 10.1002/cctc.201600407
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Synthesis of Oxazolidinones from Epoxides and Isocyanates Catalyzed by Rare-Earth-Metal Complexes.
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- ChemCatChem, 2015, v. 7, n. 7, p. 1145, doi. 10.1002/cctc.201403015
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A green approach for the synthesis of 2-oxazolidinones using gold(I) complex immobilized on KCC-1 as nanocatalyst at room temperature.
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- Applied Organometallic Chemistry, 2016, v. 30, n. 10, p. 835, doi. 10.1002/aoc.3511
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Theoretical Investigation of Proton Transfer in Thiazolidine-2-thione and Oxazolidine-2-thione via Direct Transition and Self-Assisted and Water-Assisted Tautomerization.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 4, p. 361, doi. 10.1007/s10593-015-1708-3
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5-(α-Halobenzyl)- and 5-Benzylidene-2,2-dimethyl-1,3-oxazolidin-4-ones in Synthesis of α-Hydroxy Acids.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 12, p. 2801, doi. 10.1134/S1070363217120088
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'Click Synthesis' of Some Novel Benzimidazol Oxime Ethers Containing Heterocycle Residues as Potential β-Adrenergic Blocking Agents.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 12, p. 1097, doi. 10.1002/jccs.201500244
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Spirulina (Arthrospira) platensis Supported Ionic Liquid as a Catalyst for the Synthesis of 3-Aryl-2-oxazolidinones from Carbon Dioxide, Epoxide, Anilines.
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- Catalysis Letters, 2018, v. 148, n. 1, p. 119, doi. 10.1007/s10562-017-2217-z
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N-Heterocyclic Carbene (NHC) Catalyzed Cycloaddition of CO<sub>2</sub> to N-Tosyl Aziridines: Regio and Stereoselective Synthesis of Oxazolidin-2-ones.
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- ChemCatChem, 2012, v. 4, n. 6, p. 774, doi. 10.1002/cctc.201200080
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An Experimental and Theoretical Study on the Unexpected Catalytic Activity of Triethanolamine for the Carboxylative Cyclization of Propargylic Amines with CO<sub>2</sub>.
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- ChemSusChem, 2017, v. 10, n. 9, p. 2001, doi. 10.1002/cssc.201700241
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Cyanuric Acid-Based Organocatalyst for Utilization of Carbon Dioxide at Atmospheric Pressure.
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- ChemSusChem, 2017, v. 10, n. 6, p. 1080, doi. 10.1002/cssc.201601684
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Formal Synthesis of (–)‐Perhydrohistrionicotoxin Using a Thorpe‐Ziegler Cyclization Approach. Synthesis of Functionalized Aza‐Spirocycles.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 6, p. 1215, doi. 10.1002/ejoc.201801604
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Synthesis and In Vitro Antibacterial Activity of Novel 3-Azabicyclo[3.3.0]octanyl Oxazolidinones.
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- Chemical Biology & Drug Design, 2012, v. 80, n. 3, p. 388, doi. 10.1111/j.1747-0285.2012.01404.x
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Discovery, Synthesis and Evaluation of Novel Cholesterol Absorption Inhibitors.
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- Chemical Biology & Drug Design, 2012, v. 80, n. 3, p. 426, doi. 10.1111/j.1747-0285.2012.01421.x
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The synthesis of sutezolid and eperezolid using proline catalyzed α-aminoxylation of an aldehyde.
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- Journal of Chemical Sciences, 2022, v. 134, n. 2, p. 1, doi. 10.1007/s12039-022-02052-2
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Synthesis and Biological Evaluation of Novel Dehydroabietic Acid-Oxazolidinone Hybrids for Antitumor Properties.
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- International Journal of Molecular Sciences, 2018, v. 19, n. 10, p. 3116, doi. 10.3390/ijms19103116
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A Metal-Free Approach Toward Saturated N-Propargyl Heterocycles via an Annulation/Decarboxylative Coupling Sequence.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 11, p. 2447, doi. 10.1002/adsc.201500044
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Oxazolidinone Synthesis through Halohydrin Dehalogenase- Catalyzed Dynamic Kinetic Resolution.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 8, p. 1709, doi. 10.1002/adsc.201500111
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Oxazolidinone Antibiotics: Chemical, Biological and Analytical Aspects.
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- Molecules, 2021, v. 26, n. 14, p. 4280, doi. 10.3390/molecules26144280
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In Vitro Activities of LCB 01-0648, a Novel Oxazolidinone, against Gram-Positive Bacteria.
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- Molecules, 2017, v. 22, n. 3, p. 394, doi. 10.3390/molecules22030394
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A Novel Synthesis of the Oxazolidinone Antithrombotic Agent Rivaroxaban.
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- Molecules, 2014, v. 19, n. 9, p. 14999, doi. 10.3390/molecules190914999
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Absolute Configuration of the Phenylpropanoid Isolated from Peperomia tetraphylla.
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- Chinese Journal of Chemistry, 2013, v. 31, n. 10, p. 1336, doi. 10.1002/cjoc.201300648
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- Article
Isocyanurate Formation During Oxazolidinone Synthesis from Epoxides and Isocyanates Catalysed by a Chromium(Salphen) Complex.
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- Chemistry - A European Journal, 2017, v. 23, n. 52, p. 12937, doi. 10.1002/chem.201702948
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A One-Pot Synthesis of N-Aryl-2-Oxazolidinones and Cyclic Urethanes by the Lewis Base Catalyzed Fixation of Carbon Dioxide into Anilines and Bromoalkanes.
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- Chemistry - A European Journal, 2016, v. 22, n. 30, p. 10355, doi. 10.1002/chem.201602338
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- Article
Generation of Oxazolidine-2,4-diones Bearing Sulfur-Substituted Quaternary Carbon Atoms by Oxothiolation/Cyclization of Ynamides.
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- Chemistry - A European Journal, 2016, v. 22, n. 7, p. 2532, doi. 10.1002/chem.201504356
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Lewis-Acid-Mediated Stereospecific Radical Polymerization of Acrylimides Bearing Chiral Oxazolidinones.
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- Chemistry - A European Journal, 2015, v. 21, n. 51, p. 18547, doi. 10.1002/chem.201504184
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Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines.
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- Chemistry - A European Journal, 2015, v. 21, n. 29, p. 10530, doi. 10.1002/chem.201501271
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Direct Assembly of 2-Oxazolidinones by Chemical Fixation of Carbon Dioxide.
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- Chemistry - A European Journal, 2014, v. 20, n. 29, p. 8867, doi. 10.1002/chem.201402368
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(Enantio)selective Hydrogen Autotransfer: Ruthenium-Catalyzed Synthesis of Oxazolidin-2-ones from Urea and Diols.
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- Angewandte Chemie, 2016, v. 128, n. 27, p. 7957, doi. 10.1002/ange.201600698
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Transformation of Atmospheric CO<sub>2</sub> Catalyzed by Protic Ionic Liquids: Efficient Synthesis of 2-Oxazolidinones.
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- Angewandte Chemie, 2015, v. 127, n. 18, p. 5489, doi. 10.1002/ange.201411969
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A Rapid Synthesis of 4-Oxazolidinones: Total Synthesis of Synoxazolidinones A and B.
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- Angewandte Chemie, 2014, v. 126, n. 21, p. 5505, doi. 10.1002/ange.201402310
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Highly Diastereoselective Total Syntheses of (+)-7-Epigoniodiol, (−)-8-Epigoniodiol, and (+)-9-Deoxygoniopypyrone.
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- Helvetica Chimica Acta, 2013, v. 96, n. 7, p. 1366, doi. 10.1002/hlca.201200368
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Stereocontrolled Synthesis of the C1-C10 Fragments of Monensin B and Laidlomycin.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 6, p. 567, doi. 10.1002/ajoc.201500078
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- Article
Novel approach to stereoselective synthesis of ( E)/( Z)-( N-acyl-oxazolidinone)-eneglycinates.
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- Research on Chemical Intermediates, 2015, v. 41, n. 2, p. 749, doi. 10.1007/s11164-013-1225-x
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A convenient one-pot synthesis and bioactivity of N-dichloroacetyl-5-aryl-1,3-oxazolidines.
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- Heterocyclic Communications, 2013, v. 19, n. 3, p. 201, doi. 10.1515/hc-2013-0042
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- Article
Expanded Ring NHC Silver Carboxylate Complexes as Efficient and Reusable Catalysts for the Carboxylative Cyclization of Unsubstituted Propargylic Derivatives.
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- ChemSusChem, 2021, v. 14, n. 11, p. 2367, doi. 10.1002/cssc.202002822
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- Article
Synthesis of Oxazolidinones by using Carbon Dioxide as a C<sub>1</sub> Building Block and an Aluminium‐Based Catalyst.
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- ChemSusChem, 2019, v. 12, n. 14, p. 3296, doi. 10.1002/cssc.201901171
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