Works matching DE "RESOLUTION (Chemistry)"
Results: 480
O,O'-Di-p-toluoyl-(2R,3R)-tartaric acid as supramolecular resolving agent.
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- Journal of Thermal Analysis & Calorimetry, 2003, v. 74, n. 1, p. 155, doi. 10.1023/A:1026334021007
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Symmetry, inertness and chirality in theory of chiral systems.
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- Foundations of Chemistry, 2015, v. 17, n. 2, p. 129, doi. 10.1007/s10698-015-9231-2
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Asymmetric reduction of ketopantolactone using a strictly ( R)-stereoselective carbonyl reductase through efficient NADPH regeneration and the substrate constant-feeding strategy.
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- Biotechnology Letters, 2017, v. 39, n. 11, p. 1741, doi. 10.1007/s10529-017-2415-1
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Chemical Electron Tomography at Lower Dose and Higher Resolution.
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- Microscopy & Microanalysis, 2024, v. 30, p. 1, doi. 10.1093/mam/ozae044.890
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Optical Resolution and Structure Determination of New Indolizidine Alkaloids from Elaeocarpus sphaericus.
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- Helvetica Chimica Acta, 2011, v. 94, n. 2, p. 347, doi. 10.1002/hlca.201000200
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Novel Naphthoquinones from Heterophragma adenophyllum.
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- Helvetica Chimica Acta, 2004, v. 87, n. 4, p. 820
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Identification of transcription factor binding sites from ChIP-seq data at high resolution.
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- Bioinformatics, 2013, v. 29, n. 21, p. 2705, doi. 10.1093/bioinformatics/btt470
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功能性二氧化硅微球的制备及对色氨酸 对映体的高效拆分研究.
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- Journal of Changzhou University (Natural Science Edition) / Changzhou Daxue Xuebao (Ziran Kexue Ban), 2019, v. 31, n. 6, p. 17, doi. 10.3969/j.issn.2095-0411.2019.06.003
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Chiral resolution, determination of absolute configuration, and biological evaluation of (1,2-benzothiazin-4-yl)acetic acid enantiomers as aldose reductase inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 5, p. 846, doi. 10.3109/14756366.2014.961447
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Lipase-mediated Resolution of Branched Chain Fatty Acids.
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- Biocatalysis & Biotransformation, 2002, v. 20, n. 5, p. 297, doi. 10.1080/10242420290025511
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Microbial Oxidation of Amines: A Preliminary Investigation on the Resolution of Racemic 1-Phenylethyl Amine.
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- Biocatalysis & Biotransformation, 2002, v. 20, n. 5, p. 311
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Mini Review: Advances in 2-Haloacid Dehalogenases.
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- Frontiers in Microbiology, 2021, v. 12, p. 1, doi. 10.3389/fmicb.2021.758886
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Discovery of Cymopolyphenols A–F From a Marine Mesophotic Zone Aaptos Sponge-Associated Fungus Cymostachys sp. NBUF082.
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- Frontiers in Microbiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fmicb.2021.638610
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Medical Uncertainty and Paradox, and the Quality-of-Care Crisis.
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- International Journal of Health, Wellness & Society, 2012, v. 2, n. 1, p. 21, doi. 10.18848/2156-8960/CGP/v02i01/41210
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High Resolution Chemistry Transport Modeling with the On-Line CHIMERE-WRF Model over the French Alps—Analysis of a Feedback of Surface Particulate Matter Concentrations on Mountain Meteorology.
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- Atmosphere, 2020, v. 11, n. 6, p. 565, doi. 10.3390/atmos11060565
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Coupled Stratospheric Chemistry–Meteorology Data Assimilation. Part I: Physical Background and Coupled Modeling Aspects.
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- Atmosphere, 2020, v. 11, n. 2, p. 150, doi. 10.3390/atmos11020150
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Resolution enhancement of field asymmetric waveform ion mobility spectrometry (FAIMS) by ion focusing.
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- Chemistry Central Journal, 2013, v. 7, n. 1, p. 1, doi. 10.1186/1752-153X-7-120
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Synthesis of Adamantyl H‐Phosphinate Esters.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 1, p. 1, doi. 10.1002/ejoc.202101130
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Combining Diastereomeric Resolution and Viedma Ripening by Using a Racemic Resolving Agent.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 44, p. 5975, doi. 10.1002/ejoc.202101193
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Regioselective Synthesis of 4,7,12,15‐Tetrasubstituted [2.2]Paracyclophanes: A Modular Route Involving Optical Resolution.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 34, p. 4828, doi. 10.1002/ejoc.202100762
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Synthesis, Chiral Resolution, and Optical Properties of 2,18‐Dihydoxy‐5,10,15‐trioxa[9]helicene.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 1, p. 146, doi. 10.1002/ejoc.202001177
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A Decade of Muricatacin Synthesis and Beyond.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 44, p. 6845, doi. 10.1002/ejoc.202000665
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Helicenes Fused with Hexafluorocyclopentene (HFCP): Synthesis, Structure, and Properties.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 12, p. 1871, doi. 10.1002/ejoc.202000152
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Desymmetrization of 2‐Cyano‐N‐tosylbenzylidenimine with Thiols and Organocatalytic Heterocyclization by Dynamic Resolution: Mechanism Investigation.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 46, p. 7584, doi. 10.1002/ejoc.201901499
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First Direct Evidence of an ortho‐Lithiated Aryloxetane: Solid and Solution Structure, and Dynamics.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5549, doi. 10.1002/ejoc.201900949
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Cover Feature: Rare‐Earth‐Metal‐Catalyzed Kinetic Resolution of Chiral Aminoalkenes via Hydroamination: The Effect of the Silyl Substituent of the Binaphtholate Ligand on Resolution Efficiency (Eur. J. Org. Chem. 15/2019).
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 15, p. 2567, doi. 10.1002/ejoc.201900455
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Rare‐Earth‐Metal‐Catalyzed Kinetic Resolution of Chiral Aminoalkenes via Hydroamination: The Effect of the Silyl Substituent of the Binaphtholate Ligand on Resolution Efficiency.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 15, p. 2592, doi. 10.1002/ejoc.201900107
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Chiral Tetraaryl‐ and Tetraalkynylborates as Chiral Solvating Agents for Tetraalkylammonium Salts.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 4, p. 803, doi. 10.1002/ejoc.201801448
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Optically Active 2,7,10,15‐Tetrahydroxytetraphenylene: Clathrates with Both Enantiomers of 1‐Phenylethylamine and Their Stability.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 48, p. 6991, doi. 10.1002/ejoc.201801422
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Bio‐Based Chiral Amines via Aza‐Michael Additions to (–)‐Levoglucosenone Under Aqueous Conditions.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 17, p. 2028, doi. 10.1002/ejoc.201800388
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Configurationally Stable (S)- and (R)-α-Methylproline-Derived Ligands for the Direct Chemical Resolution of Free Unprotected β³-Amino Acids.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 15, p. 1821, doi. 10.1002/ejoc.201800120
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Lipase Regioselective O-Acetylations of a myo-Inositol Derivative: Efficient Desymmetrization of 1,3-Di-O-benzyl-myoinositol.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 3, p. 386, doi. 10.1002/ejoc.201701417
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Total Synthesis and Cytotoxic Activity of 5′-Hydroxyzearalenone and 5′β-Hydroxyzearalenone.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 47, p. 7133, doi. 10.1002/ejoc.201701272
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First and Highly Stereoselective Synthesis of Both Enantiomers of Octahydroindole-2-phosphonic Acid (Oic<sup>P</sup>).
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 45, p. 6781, doi. 10.1002/ejoc.201701330
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Covalently Immobilized Lipases are Efficient Stereoselective Catalysts for the Kinetic Resolution of rac-(5-Phenylfuran-2-yl)-β-alanine Ethyl Ester Hydrochlorides.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 20, p. 2878, doi. 10.1002/ejoc.201700174
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Synthesis and Chiral Resolution of C<sub>3</sub>-Symmetric Tribenzotriquinacenes.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 26, p. 4470, doi. 10.1002/ejoc.201600890
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Graphical Abstract: Eur. J. Org. Chem. 33/2015.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 33, p. 7183, doi. 10.1002/ejoc.201590096
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One-Pot Synthesis, Crystallization and Deracemization of Isoindolinones from Achiral Reactants.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 33, p. 7249, doi. 10.1002/ejoc.201501191
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Ultrahigh-Resolution Diffusion-Ordered Spectroscopy.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 50, p. 15579, doi. 10.1002/anie.201609676
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Combining Organocatalysis with Central-to-Axial Chirality Conversion: Atroposelective Hantzsch-Type Synthesis of 4-Arylpyridines.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 4, p. 1401, doi. 10.1002/anie.201509967
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Insights into the Mechanism of Carbon Monoxide Dehydrogenase at Atomic Resolution.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 29, p. 8337, doi. 10.1002/anie.201503979
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Do Spatially Explicit Wildlife Exposure Models Improve the Estimation of Risk for Small Mammals? Case Study: Application of Spatially Explicit Exposure Model to Small Mammal Exposures to Lead in Heterogeneous Landscapes.
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- Integrated Environmental Assessment & Management, 2021, v. 17, n. 1, p. 259, doi. 10.1002/ieam.4326
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Sensitivity of CHIMERE to changes in model resolution and chemistry over the northwestern Iberian Peninsula.
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- Atmospheric Chemistry & Physics Discussions, 2019, p. 1, doi. 10.5194/acp-2019-351
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New analytical approach to calibrate the NaI (Tl) detectors using spherical radioactive sources.
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- Radiation Protection Dosimetry, 2013, v. 156, n. 1, p. 109, doi. 10.1093/rpd/nct048
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Kinetic Analysis of R-Selective ω-Transaminases for Determination of Intrinsic Kinetic Parameters and Computational Modeling of Kinetic Resolution of Chiral Amine.
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- Applied Biochemistry & Biotechnology, 2020, v. 191, n. 1, p. 92, doi. 10.1007/s12010-020-03240-x
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Resolution enhanced homonuclear carbon decoupled triple resonance experiments for unambiguous RNA structural characterization.
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- Journal of Biomolecular NMR, 2005, v. 32, n. 2, p. 129, doi. 10.1007/s10858-005-5093-6
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α, β-DCP-LA Selectively Activates PKC-ε and Stimulates Neurotransmitter Release with the Highest Potency among 4 Diastereomers.
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- Cellular Physiology & Biochemistry (Karger AG), 2011, v. 27, n. 2, p. 149, doi. 10.1159/000325217
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Crystal Engineering of Conglomerates: Dilution of Racemate-Forming Fe(II) and Ni(II) Congeners into Conglomerate-Forming [Zn(bpy) 3 ](PF 6) 2.
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- Chemistry (2624-8549), 2023, v. 5, n. 1, p. 255, doi. 10.3390/chemistry5010020
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A magneto-optical scheme of a proton microscope based on the U-70 synchrotron radiograph complex.
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- Technical Physics Letters, 2016, v. 42, n. 7, p. 674, doi. 10.1134/S1063785016070105
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Multisyringe Chromatography (MSC): An Effective and Low Cost Tool for Water-Soluble Vitamin Separation.
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- Analytical Letters, 2012, v. 45, n. 17, p. 2637, doi. 10.1080/00032719.2012.693139
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