Works matching DE "ACETONE"
Results: 3929
Towards a high-quality in situ observation network for oxygenated volatile organic compounds (OVOCs) in Europe: transferring metrological traceability to the field.
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- Atmospheric Measurement Techniques, 2025, v. 18, n. 2, p. 371, doi. 10.5194/amt-18-371-2025
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2.7μm 增透膜设计及工艺研究.
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- Piezoelectrics & Acoustooptics, 2024, v. 46, n. 6, p. 990, doi. 10.11977/j.issn.1004-2474.2024.06.025
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Simultaneous Spectrometric Determination of Cu(II), Co(II), and Ni(II) in Pharmaceutical and Environmental Samples with XAD-4/DMMDTC Solid-Phase Extraction System.
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- Biological Trace Element Research, 2020, v. 194, n. 1, p. 295, doi. 10.1007/s12011-019-01930-0
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Metalloproteomics Approach to Analyze Mercury in Breast Milk and Hair Samples of Lactating Women in Communities of the Amazon Basin, Brazil.
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- Biological Trace Element Research, 2018, v. 181, n. 2, p. 216, doi. 10.1007/s12011-017-1057-4
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News and Analysis of the Global Innovation Scene.
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- Research Technology Management, 2020, v. 63, n. 3, p. 2, doi. 10.1080/08956308.2020.1733883
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Properties of Rice Stem Extracts Obtained by Using Subcritical Fluids.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 10, p. 2112, doi. 10.1271/bbb.130485
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Extraction of Defatted Rice Bran with Subcritical Aqueous Acetone.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 8, p. 1535, doi. 10.1271/bbb.120286
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Functional-Food Constituents in the Fruiting Bodies of Stropharia rugosoannulata.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 8, p. 1631, doi. 10.1271/bbb.110308
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Synthesis of Quinolactacide via an Acyl Migration Reaction and Dehydrogenation with Manganese Dioxide, and Its Insecticidal Activities.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 1, p. 303, doi. 10.1271/bbb.70.303
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Fabrication of functionally graded 3A/5A zeolites by electrophoretic deposition.
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- Surface Engineering, 2007, v. 23, n. 6, p. 443, doi. 10.1179/174329407X247136
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Electrochemical Nonenzymatic Acetone Sensing: A Novel Approach of Biosensor Platform Based on CNT/CuO Nanosystems.
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- Macromolecular Symposia, 2023, v. 412, n. 1, p. 1, doi. 10.1002/masy.202200150
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Caulerpa lentillifera Seaweed Extract as Natural Sensitizer for Dye‐Sensitized Solar Cell.
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- Macromolecular Symposia, 2023, v. 407, n. 1, p. 1, doi. 10.1002/masy.202100359
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- Article
Non‐Invasive Diabetic Sensor Based on Cellulose Acetate/Graphene Nanocomposite.
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- Macromolecular Symposia, 2020, v. 392, n. 1, p. 1, doi. 10.1002/masy.202000024
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Metal‐Chitosan Nanocomposites: A Perspective Way to Preparation, Morphology, and Structural Studies.
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- Macromolecular Symposia, 2020, v. 389, n. 1, p. 1, doi. 10.1002/masy.201900067
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Asymmetric Aldol Reaction of Thiazole-Carbaldehydes: Regio- and Stereoselective Synthesis of Tubuvalin Analogues.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 16, p. 3370, doi. 10.1002/adsc.201400640
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Ferrocenyl-Based P,N Catalysts for the Mono-α-Arylation of Acetone.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 14/15, p. 2979, doi. 10.1002/adsc.201400235
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Direct Organocatalytic Asymmetric Mannich Addition of 3-Substituted-2 H-1,4-Benzoxazines: Access to Tetrasubstituted Carbon Stereocenters.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 17, p. 3381, doi. 10.1002/adsc.201300654
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Femtosecond laser inscription of polarized-sensitive volume phase grating in nanoporous glass.
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- Optical & Quantum Electronics, 2023, v. 55, n. 5, p. 1, doi. 10.1007/s11082-023-04590-6
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Dye-sensitized solar cells concocted with dyes extracted from fresh and dried leaves of Henna using different solvents.
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- Optical & Quantum Electronics, 2021, v. 53, n. 5, p. 1, doi. 10.1007/s11082-021-02953-5
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Adsorption profile and thermodynamic parameters of the preconcentration of Eu(III) on 2-thenoyltrifluoroacetone loaded polyurethane (PUR) foam.
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- Journal of Radioanalytical & Nuclear Chemistry, 2003, v. 256, n. 1, p. 73, doi. 10.1023/A:1023300109423
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Comparative analysis of various fixative solutions on insect preservation for molecular studies.
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- Entomologia Experimentalis et Applicata, 2009, v. 130, n. 3, p. 290, doi. 10.1111/j.1570-7458.2008.00821.x
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Immobilization of Baeyer–Villiger monooxygenase from acetone grown Fusarium sp.
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- Biotechnology Letters, 2022, v. 44, n. 3, p. 461, doi. 10.1007/s10529-022-03224-3
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Umbelliferone esters with antibacterial activity produced by lipase-mediated biocatalytic pathway.
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- Biotechnology Letters, 2021, v. 43, n. 2, p. 469, doi. 10.1007/s10529-020-03014-9
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Influence of organic solvents in the extraction and purification of torularhodin from Sporobolomyces ruberrimus.
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- Biotechnology Letters, 2021, v. 43, n. 1, p. 89, doi. 10.1007/s10529-020-03023-8
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An engineered non-oxidative glycolysis pathway for acetone production in Escherichia coli.
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- Biotechnology Letters, 2016, v. 38, n. 8, p. 1359, doi. 10.1007/s10529-016-2115-2
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Assessment of morphological changes of Clostridium acetobutylicum by flow cytometry during acetone/butanol/ethanol extractive fermentation.
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- Biotechnology Letters, 2015, v. 37, n. 3, p. 577, doi. 10.1007/s10529-014-1702-3
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Extraction of short-chain-length poly-[( R)-hydroxyalkanoates] ( scl-PHA) by the 'anti-solvent' acetone under elevated temperature and pressure.
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- Biotechnology Letters, 2013, v. 35, n. 7, p. 1023, doi. 10.1007/s10529-013-1185-7
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Lipase-catalyzed simultaneous biosynthesis of biodiesel and glycerol carbonate from corn oil in dimethyl carbonate.
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- Biotechnology Letters, 2011, v. 33, n. 9, p. 1789, doi. 10.1007/s10529-011-0627-3
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Lipase-catalyzed selective synthesis of monolauroyl maltose using continuous stirred tank reactor.
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- Biotechnology Letters, 2008, v. 30, n. 3, p. 497, doi. 10.1007/s10529-007-9560-x
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Anaerobic biotechnological approaches for production of liquid energy carriers from biomass.
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- Biotechnology Letters, 2007, v. 29, n. 7, p. 1005, doi. 10.1007/s10529-007-9360-3
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Adsorbents for acetone in cyclohexane effuent employed in Ziegler-Natta catalyst process.
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- Adsorption, 2008, v. 14, n. 6, p. 805, doi. 10.1007/s10450-008-9143-8
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Enhancing mechanical properties and surface quality of FDM-printed ABS: A comprehensive study on cold acetone vapor treatment.
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- International Journal of Advanced Manufacturing Technology, 2024, v. 130, n. 7/8, p. 4027, doi. 10.1007/s00170-023-12929-2
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Surface roughness of FDM parts after post-processing with acetone vapor bath smoothing process.
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- International Journal of Advanced Manufacturing Technology, 2018, v. 95, n. 1-4, p. 1505, doi. 10.1007/s00170-017-1165-5
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Theoretical study of the side reactions of ethanol-to-butadiene conversion on MgO catalyst: formation of diethyl ether, ethyl acetal, 1,3-butanediol, methyl ethyl ketone, n-butanol, butanal, and acetone.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2022, v. 141, n. 11, p. 1, doi. 10.1007/s00214-022-02927-0
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A force field for acetone: the transition from small clusters to liquid phase investigated by molecular dynamics simulations.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 7, p. 1, doi. 10.1007/s00214-016-1914-9
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On the possible catalytic role of a single water molecule in the acetone + OH gas phase reaction: a theoretical pseudo-second-order kinetics study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2011, v. 129, n. 2, p. 209, doi. 10.1007/s00214-011-0921-0
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Theoretical studies and rate constants calculation for the reactions of acetone with fluorine and bromine atoms.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2011, v. 128, n. 3, p. 317, doi. 10.1007/s00214-010-0848-x
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Direct ab initio MD study on the hydrogen abstraction reaction of triplet state acetone from methanol molecule.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2011, v. 128, n. 2, p. 207, doi. 10.1007/s00214-010-0822-7
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Theoretical studies on the reactions of acetone with chlorine atom and methyl radical.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2008, v. 119, n. 5/6, p. 445, doi. 10.1007/s00214-007-0402-7
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Theoretical modeling of spectroscopic properties of molecules in solution: toward an effective dynamical discrete/continuum approach.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2007, v. 117, n. 5/6, p. 1001, doi. 10.1007/s00214-006-0216-z
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Hybrid Monte Carlo simulations of vertical electronic transitions in acetone in aqueous solution.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2007, v. 117, n. 3, p. 441, doi. 10.1007/s00214-006-0172-7
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Solvent Effects on the UV (n → π*) and NMR (<sup>17</sup>O) Spectra of Acetone in Aqueous Solution: Development and Validation of a Modified A MBER Force Field for an Integrated MD/DFT/PCM Approach.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2006, v. 116, n. 4/5, p. 456, doi. 10.1007/s00214-006-0098-0
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An application of second-order n-electron valence state perturbation theory to the calculation of excited states.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2004, v. 111, n. 2-6, p. 352, doi. 10.1007/s00214-003-0549-9
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Theoretical investigation on the oxazaborolidine-ketone interaction in small model systems.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2004, v. 111, n. 2-6, p. 287, doi. 10.1007/s00214-003-0538-z
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- Article
Formal Synthesis of (−)-Cephalotaxine.
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- Helvetica Chimica Acta, 2012, v. 95, n. 12, p. 2502, doi. 10.1002/hlca.201200486
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- Article
Microwave-Assisted Stereoselective 1,3-Dipolar Cycloaddition of C, N-Diarylnitrone ( i.e., N-(Arylmethylidene)benzenamine N-Oxide) and Bis(arylmethylidene)acetone (=1,5-Diarylpenta-1,4-dien-3-one): NMR and Crystal Analysis of Diastereoisomeric Bis(isoxazolidines)
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- Helvetica Chimica Acta, 2012, v. 95, n. 1, p. 173, doi. 10.1002/hlca.201100263
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New and Bioactive Sesquiterpenes from Schisandra sphenanthera.
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- Helvetica Chimica Acta, 2011, v. 94, n. 12, p. 2295, doi. 10.1002/hlca.201100205
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Reactions of Imidoyl Isoselenocyanates with Aromatic 2-Amino N-Heterocycles and 1-Methyl-1 H-imidazole.
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- Helvetica Chimica Acta, 2011, v. 94, n. 9, p. 1575, doi. 10.1002/hlca.201100230
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Two New Monoterpenes from Mentha haplocalyx.
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- Helvetica Chimica Acta, 2010, v. 93, n. 12, p. 2495, doi. 10.1002/hlca.201000143
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A Novel Trypsin-Catalyzed Three-Component Mannich Reaction.
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- Helvetica Chimica Acta, 2010, v. 93, n. 11, p. 2231, doi. 10.1002/hlca.201000063
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- Article