oxazolidin-2-one has been researched along with carbamates in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 6 (40.00) | 29.6817 |
2010's | 8 (53.33) | 24.3611 |
2020's | 1 (6.67) | 2.80 |
Authors | Studies |
---|---|
Beak, P; Gross, KM | 1 |
Ballester, P; Far, AR; Rebek, J; Shivanyuk, A | 1 |
Adam, W; Franz, R; Inoue, Y; Jockusch, S; Martinez, C; Poon, T; Sivaguru, J; Turro, NJ; Washington, I | 1 |
Adam, W; Dyer, J; Inoue, Y; Jockusch, S; Saito, H; Sivaguru, J; Turro, NJ | 1 |
Bernard, SE; Decatur, JD; Gupta, R; Rojas, CM; Sogi, KM | 1 |
Candler, J; Doran, AC; Duplantier, AJ; Efremov, I; Ganong, AH; Haas, JA; Hanks, AN; Kraus, KG; Lazzaro, JT; Lu, J; Maklad, N; McCarthy, SA; O'Sullivan, TJ; Rogers, BN; Siuciak, JA; Spracklin, DK; Zhang, L | 1 |
Costache, A; Kaushik, D; Michniak-Kohn, B | 1 |
Li, X; Lu, M; Lu, Y; Zeng, X; Zhong, G; Zhu, D | 1 |
Baudot, R; Cren-Olivé, C; Feidt, C; Fratta, C; Lazartigues, A; Thomas, M; Wiest, L | 1 |
Harding, SL; Savage, GP | 1 |
Wang, GW; You, X | 1 |
Frost, CG; Mahy, W; Plucinski, PK | 1 |
Bethel, TK; Giletto, MB; Jones, CL; Kuszpit, MR; Tepe, JJ | 1 |
Chamni, S; Chanvorachote, P; Plubrukrn, A; Saito, N; Sirimangkalakitti, N; Suwanborirux, K; Yokoya, M | 1 |
Bansagi, J; Batey, RA; Debrauwer, V; Narayanan, P; Wilson-Konderka, C | 1 |
15 other study(ies) available for oxazolidin-2-one and carbamates
Article | Year |
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Complex-induced proximity effects: the effect of varying directing-group orientation on carbamate-directed lithiation reactions.
Topics: Bridged Bicyclo Compounds; Carbamates; Ligands; Lithium; Models, Molecular; Molecular Structure; Oxazolidinones; Stereoisomerism; Tin | 2001 |
A synthetic receptor for choline and carnitine.
Topics: Carbamates; Carnitine; Choline; Crystallography, X-Ray; Models, Molecular; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Oxazolidinones; Receptors, Cell Surface | 2002 |
Temperature and solvent control of the stereoselectivity in the reactions of singlet oxygen with oxazolidinone-substituted enecarbamates.
Topics: Benzoin; Carbamates; Kinetics; Oxazolidinones; Photochemistry; Singlet Oxygen; Solvents; Stereoisomerism; Temperature; Thermodynamics | 2004 |
Controlled diastereoselectivity at the alkene-geometry through selective encapsulation: E-Z photoisomerization of oxazolidinone-functionalized enecarbamates within hydrophobic nano-cavities.
Topics: Alkenes; Carbamates; Circular Dichroism; Indicators and Reagents; Isomerism; Magnetic Resonance Spectroscopy; Oxazolidinones; Photochemistry; Solutions; Stereoisomerism | 2007 |
Protecting group and solvent control of stereo- and chemoselectivity in glucal 3-carbamate amidoglycosylation.
Topics: Calcium Gluconate; Carbamates; Catalysis; Combinatorial Chemistry Techniques; Glycosylation; Hexosamines; Mannose; Molecular Structure; Oxazolidinones; Stereoisomerism | 2009 |
3-Benzyl-1,3-oxazolidin-2-ones as mGluR2 positive allosteric modulators: Hit-to lead and lead optimization.
Topics: Administration, Oral; Allosteric Regulation; Allosteric Site; Carbamates; Chemistry, Pharmaceutical; Drug Design; Humans; Inhibitory Concentration 50; Ligands; Microsomes; Models, Chemical; Molecular Structure; Oxazolidinones; Receptors, Metabotropic Glutamate; Schizophrenia | 2009 |
Percutaneous penetration modifiers and formulation effects.
Topics: Administration, Cutaneous; Azepines; Cadaver; Carbamates; Ceramides; Chemistry, Pharmaceutical; DEET; Drug Compounding; Ethanol; Humans; Hydrogen Bonding; Insect Repellents; Kinetics; Models, Molecular; Molecular Structure; Oxazolidinones; Permeability; Pharmaceutic Aids; Polyethylene Glycols; Propylene Glycol; Skin; Skin Absorption; Solvents; Structure-Activity Relationship; Sulfur Compounds; Technology, Pharmaceutical; Water | 2010 |
Chiral Brønsted acid catalyzed enantioselective α-aminoxylation of enecarbamates.
Topics: Acids; Amino Alcohols; Carbamates; Catalysis; Ketones; Nitroso Compounds; Oxazolidinones; Stereoisomerism | 2010 |
Multiresidue method for the determination of 13 pesticides in three environmental matrices: water, sediments and fish muscle.
Topics: Acetamides; Aminoimidazole Carboxamide; Animals; Benzimidazoles; Carbamates; Chemical Fractionation; Chromatography, Liquid; Environmental Monitoring; Fishes; Geologic Sediments; Hydantoins; Isoxazoles; Methacrylates; Muscles; Naphthalenes; Niacinamide; Oxazolidinones; Pesticide Residues; Pesticides; Phenylurea Compounds; Propionates; Pyrimidines; Quinoxalines; Reproducibility of Results; Solid Phase Extraction; Strobilurins; Sulfonylurea Compounds; Tandem Mass Spectrometry; Thiophenes; Water Pollutants, Chemical | 2011 |
Facial selectivity induced by N-aryl atropisomerism in benzonitrile oxide cycloadditions with 4-methylene-2-oxazolidinones.
Topics: Carbamates; Cyclization; Methylation; Models, Molecular; Molecular Structure; Nitriles; Oxazolidinones; Oxides; Stereoisomerism | 2012 |
Ferric chloride-catalyzed reaction of [60]fullerene with tert-butyl N-substituted carbamates: synthesis of oxazolidino[4,5:1,2][60]fullerenes.
Topics: Carbamates; Catalysis; Chlorides; Ferric Compounds; Fullerenes; Magnetic Resonance Spectroscopy; Oxazolidinones | 2014 |
Copper-catalyzed one-pot synthesis of N-aryl oxazolidinones from amino alcohol carbamates.
Topics: Amino Alcohols; Carbamates; Catalysis; Copper; Cyclization; Hydrocarbons, Iodinated; Molecular Structure; Oxazolidinones | 2014 |
Hydroxyamination of olefins using Br-N-(CO2Me)2.
Topics: Alkenes; Amination; Amino Alcohols; Carbamates; Catalysis; Cyclization; Indicators and Reagents; Magnetic Resonance Spectroscopy; Oxazolidinones; Stereoisomerism | 2015 |
Synthesis and Absolute Configuration of Acanthodendrilline, a New Cytotoxic Bromotyrosine Alkaloid from the Thai Marine Sponge Acanthodendrilla sp.
Topics: Animals; Antineoplastic Agents; Carbamates; Cell Line, Tumor; Humans; Magnetic Resonance Spectroscopy; Mass Spectrometry; Oxazolidinones; Porifera; Spectroscopy, Fourier Transform Infrared; Stereoisomerism | 2016 |
Topics: Alcohols; Amines; Biological Products; Carbamates; Hydantoins; Isocyanates; Oxazolidinones; Thiocarbamates; Urea | 2022 |