Works matching DE "ORGANIC compounds manufacturing"
Results: 22
Microbial processes of organic matter production and decomposition in saline rivers of the Lake Elton area (Volgograd oblast, Russia).
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- Microbiology (00262617), 2018, v. 87, n. 1, p. 66, doi. 10.1134/S0026261718010095
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Production of Recalcitrant Organic Matter under the Influence of Elevated Carbon Dioxide and Temperature.
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- Water Environment Research (10614303), 2014, v. 86, n. 9, p. 779, doi. 10.2175/106143014X13975035526347
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AnSBBR Applied to the Treatment of Metalworking Fluid Wastewater: Effect of Organic and Shock Load.
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- Applied Biochemistry & Biotechnology, 2010, v. 162, n. 6, p. 1708, doi. 10.1007/s12010-010-8952-x
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New Plant In Washington To Produce Benzyl Alcohol.
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- Textile Chemist & Colorist, 1980, v. 12, n. 2, p. 8
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Fractional release factors of long-lived halogenated organic compounds in the tropical stratosphere.
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- Atmospheric Chemistry & Physics, 2010, v. 10, n. 3, p. 1093, doi. 10.5194/acp-10-1093-2010
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Remote determination of chromophoric dissolved organic matter in lakes, China.
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- International Journal of Digital Earth, 2014, v. 7, n. 11, p. 897, doi. 10.1080/17538947.2013.805261
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Synthesis of Spiropyrrolidines and Spiropyrrolizidines from Azomethine Ylides.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 4, p. 479, doi. 10.1007/s10593-014-1498-z
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Azomethine Ylides Derived from Alkyl- (3-Oxopiperazin-2-yl)Acetates in 1,3-Dipolar Cycloaddition Reactions with n-Aryl Maleimides.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 4, p. 537, doi. 10.1007/s10593-014-1504-5
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New Method for Synthesis of the Hetero-Cyclic System - 1,2,3,4-Tetrahydro-Imidazo[5,1- f][1,2,4]Triazin-7-Amine.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 4, p. 587, doi. 10.1007/s10593-014-1512-5
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FACTOR-AUGMENTED J-CURVE.
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- Journal of Economic Sciences: Theory & Practice, 2015, v. 72, n. 2, p. 4
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Production of 2,5-Diformylfuran from Biomass-derived Glucose via One-Pot Two-Step Process.
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- BioResources, 2014, v. 9, n. 3, p. 4568, doi. 10.15376/biores.9.3.4568-4580
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Efficient, One-Pot Synthesis of Tetrahydrobenzo[a]xanthen-11-ones and Dibenzo[a,j]xanthenes Using Trichloroacetic Acid as a Solid Heterogeneous Catalyst Under Solvent-Free Conditions.
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- E-Journal of Chemistry, 2011, v. 8, n. 4, p. 1895, doi. 10.1155/2011/359175
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Zeolite (ZSM-5) as a Highly Efficient and Heterogeneous Catalyst for the Synthesis of β-Enaminones and β-Enamino Esters.
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- E-Journal of Chemistry, 2011, v. 8, n. 4, p. 1632, doi. 10.1155/2011/176829
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Altering the Substrate Specificity of Reductase CgKR1 from Candida glabrata by Protein Engineering for Bioreduction of Aromatic α-Keto Esters.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 9, p. 1943, doi. 10.1002/adsc.201300775
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H-Phosphonate-Mediated Amination of Quinoline N-Oxides with Tertiary Amines: A Mild and Metal-Free Synthesis of 2-Dialkylaminoquinolines.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 9, p. 1979, doi. 10.1002/adsc.201301065
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Phenolic Esters of O-Desmethylvenlafaxine with Improved Oral Bioavailability and Brain Uptake.
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- Molecules, 2013, v. 18, n. 12, p. 14920, doi. 10.3390/molecules181214920
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OxymaPure/DIC: An Efficient Reagent for the Synthesis of a Novel Series of 4-[2-(2-Acetylaminophenyl)-2-oxo-acetylamino] Benzoyl Amino Acid Ester Derivatives.
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- Molecules, 2013, v. 18, n. 12, p. 14747, doi. 10.3390/molecules181214747
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Tips for Studies with Quantitative Morphology (Morphometry and Stereology).
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- International Journal of Morphology, 2017, v. 35, n. 4, p. 1482, doi. 10.4067/S0717-95022017000401482
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Assessment of Ovarian Follicles and Serum Reproductive Hormones in Molybdenum Trioxide Nanoparticles Treated Rats.
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- International Journal of Morphology, 2017, v. 35, n. 4, p. 1473, doi. 10.4067/S0717-95022017000401473
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Stabilisierung von hochoxidierten Upconversion-Nanopartikeln mit N-heterocyclischen Carbenen.
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- Angewandte Chemie, 2017, v. 129, n. 15, p. 4421, doi. 10.1002/ange.201611506
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Catalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C−O and C−C Bond Activation.
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- Angewandte Chemie, 2017, v. 129, n. 15, p. 4346, doi. 10.1002/ange.201611819
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Zinc-Catalyzed Dehydrogenative Cross-Coupling of Terminal Alkynes with Aldehydes: Access to Ynones.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 52, p. 15850, doi. 10.1002/anie.201509042
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