Works matching DE "CARBON disulfide"
Results: 535
O/S Exchange Reaction in Synthesizing Sulfur‐Containing Polymers.
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- Chemistry - A European Journal, 2024, v. 30, n. 42, p. 1, doi. 10.1002/chem.202401684
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- Article
Evolution of a new enzyme for carbon disulphide conversion by an acidothermophilic archaeon.
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- Nature, 2011, v. 478, n. 7369, p. 412, doi. 10.1038/nature10464
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Investigation of Fullerene Solutions by the Molecular Dynamics Method.
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- Fullerenes, Nanotubes & Carbon Nanostructures, 2008, v. 16, n. 5/6, p. 555, doi. 10.1080/15363830802286335
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Molecular and Crystal Structure of the C60F18 Adducts with Bromine and Carbon Disulfide.
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- Fullerenes, Nanotubes & Carbon Nanostructures, 2008, v. 16, n. 5/6, p. 597, doi. 10.1080/15363830802286608
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Small-angle Neutron Scattering Study of C60/CS2 Solutions.
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- Fullerenes, Nanotubes & Carbon Nanostructures, 2008, v. 16, n. 5/6, p. 616, doi. 10.1080/15363830802313014
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Fullerene Cluster Formation in Carbon Disulfide and Toluene.
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- Fullerenes, Nanotubes & Carbon Nanostructures, 2006, v. 14, n. 2/3, p. 481, doi. 10.1080/15363830600666365
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Indoor-Outdoor Distribution and Risk Assessment of Volatile Organic Compounds in the Atmosphere of Industrial and Urban Areas.
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- Environmental Toxicology, 2010, v. 25, n. 4, p. 339, doi. 10.1002/tox.20504
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Carbon Disulfide Cytotoxicity on Cultured Cardiac Myocytes of Rats.
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- Environmental Toxicology, 2002, v. 17, n. 4, p. 324, doi. 10.1002/tox.10070
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- Article
Carbonyl sulfide (COS) and carbon disulfide (CS<sub>2</sub>) exchange fluxes between cotton fields and the atmosphere in the arid area in Xinjiang, China.
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- Environmental Geochemistry & Health, 2019, v. 41, n. 5, p. 2195, doi. 10.1007/s10653-019-00268-9
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Production of carbon disulfide (CS[sub2]) from L-djenkolic acid in the roots of Mimosa pudica L.
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- Plant & Soil, 1998, v. 200, n. 1, p. 27, doi. 10.1023/A:1004212311131
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- Article
Resorcinarene-Encapsulated Gold Nanorods: Solvatochromatism and Magnetic Nanoshell Formation.
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- Supramolecular Chemistry, 2008, v. 20, n. 1/2, p. 35, doi. 10.1080/10610270701647927
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Processes of carbon disulfide degradation under the action of a pulsed corona discharge.
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- Technical Physics Letters, 2016, v. 42, n. 8, p. 822, doi. 10.1134/S1063785016080101
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AN EFFICIENT, ONE-POT SYNTHESIS OF ORGANIC DITHIOCARBAMATES USING TETRAETHYLAMMONIUM SUPEROXIDE.
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- Oxidation Communications, 2023, v. 46, n. 4, p. 1030
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Energy Utilization of Yellow Phosphorus Tail Gas: Simultaneous Catalytic Hydrolysis of Carbonyl Sulfide and Carbon Disulfide at Low Temperature.
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- Energy Technology, 2015, v. 3, n. 2, p. 136, doi. 10.1002/ente.201402122
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Structure of the Reaction Product of Anthranilic Acid Hydrazide with Carbon Disulfide in Alkaline Medium.
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- Russian Journal of Organic Chemistry, 2005, v. 41, n. 9, p. 1333, doi. 10.1007/s11178-005-0342-4
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Effective Single-Reactor Synthesis of Dithiocarbamates and Investigation of Their Flotation Properties.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S198, doi. 10.1134/S1070363223140116
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Synthesis, Some Transformations, and Antibacterial Activity of 5H-Spiro[benzo[h][1,2,4]triazolo[3,4-b]quinazoline-6,1′-cycloheptane]-7(11H)-ones.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 3, p. 485, doi. 10.1134/S1070363223030040
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Synthesis and Anticancer Activity of New Pyrimidine andOxadiazole Acyclic Nucleoside Analogs and Thiazolopyrimidine Derivatives.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 10, p. 2086, doi. 10.1134/S1070363221100261
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Functionalization of Ethyl 6-Amino-4-(4-chlorophenyl)-5-cyano-2-methyl-4H-pyran-3-carboxylate: Facile Synthesis of a New Series of Pyrano[2,3-d]pyrimidine Derivatives.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 7, p. 1403, doi. 10.1134/S1070363221070203
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Synthesis of Potential Biologically Active Compounds Based on Aryloxy- and Arylaminopropanehydrazides.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 7, p. 1181, doi. 10.1134/S1070363220070014
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Synthesis of new 3-substituted 1,3-oxazolidine-2-thiones.
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- 2017
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- Letter
Synthesis of podands modified with thiosemicarbazide and fluoroalkyl(hydroxy)pyrazoline fragments.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 5, p. 957, doi. 10.1134/S1070363217050115
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Synthesis of esters of α-vinyloxyethylcarbamodithioic acid.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 6, p. 1259, doi. 10.1134/S1070363216060074
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Synthesis of 2-amino-4-phenylthiazole-derived thiuram disulfide.
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- 2013
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- Letter
Synthesis of dithiocarbamine derivatives on the matrix of cytisine, anabasine and d-pseudoephedrine alkaloids. Crystalline structure of N-cytisine dithiocarbamate ammonium salt.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 8, p. 1716, doi. 10.1134/S1070363209080234
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- Article
Study on the Degradation of Sodium Diethyldithiocarbamate (DDTC) in Artificially Prepared Beneficiation Wastewater with Sodium Hypochlorite.
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- Journal of Chemistry, 2019, p. 1, doi. 10.1155/2019/7038015
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- Article
Oxidative stress and DNA damage in utero and embryo implantation of mice exposed to carbon disulfide at peri-implantation.
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- Human & Experimental Toxicology, 2014, v. 33, n. 4, p. 424, doi. 10.1177/0960327112474849
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- Article
Detection of germ cell genotoxic potential of carbon disulphide using sperm head shape abnormality test.
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- Human & Experimental Toxicology, 1999, v. 18, n. 12, p. 731, doi. 10.1191/096032799678839608
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Determination of the third- and fifth-order optical nonlinearities: the general case.
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- Applied Physics B: Lasers & Optics, 2014, v. 116, n. 4, p. 911, doi. 10.1007/s00340-014-5777-2
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- Article
Facile one-pot synthesis of hydroxylated 1,3-dithiane-pyrazolone hybrids.
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- Research on Chemical Intermediates, 2024, v. 50, n. 3, p. 1113, doi. 10.1007/s11164-023-05200-6
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A versatile solvent-free synthesis of novel pyrazolone-1,3-dithiolan and pyrazolone-1,3-dithiole hybrids.
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- Research on Chemical Intermediates, 2023, v. 49, n. 10, p. 4621, doi. 10.1007/s11164-023-05087-3
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- Article
Three-component coupling of boronic acids, amines, and carbon disulfide by a heterogeneous catalyst of copper (II) embedded in a highly porous and magnetic Schiff base network of melamine.
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- Research on Chemical Intermediates, 2023, v. 49, n. 10, p. 4423, doi. 10.1007/s11164-023-05081-9
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- Article
Design, Synthesis, and In Vitro Antimicrobial Evaluation of Fused Pyrano[3,2-e]tetrazolo[1,5-c]pyrimidines and Diazepines.
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- ISRN Organic Chemistry, 2013, p. 1, doi. 10.1155/2013/635384
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Synthesis and Biological Evaluation of Some Novel 5-[(3-Aralkyl Amido/Imidoalkyl) Phenyl]-1,2,4-Triazolo[3,4-b ]- 1,3,4-Thiadiazines as Antiviral Agents.
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- ISRN Organic Chemistry, 2012, p. 1, doi. 10.5402/2012/760517
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- Article
DESIGN, SYNTHESIS, MOLECULAR DOCKING, AND ANTIMICROBIAL STUDY ON NAPHTHOFURAN DERIVATIVES.
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- Rasayan Journal of Chemistry, 2023, v. 16, n. 3, p. 1613, doi. 10.31788/RJC.2023.1638459
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- Article
Nanosized molybdenum disulfide on surface‐modified carbon material as lubricating oil additive for friction‐reduction and anti‐wear.
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- Lubrication Science, 2022, v. 34, n. 2, p. 84, doi. 10.1002/ls.1573
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- Article
Dietary exposure assessment of Danish consumers to dithiocarbamate residues in food: A comparison of the deterministic and probabilistic approach.
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- Food Additives & Contaminants. Part A: Chemistry, Analysis, Control, Exposure & Risk Assessment, 2008, v. 25, n. 6, p. 714, doi. 10.1080/02652030701858262
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Monthly resolved modelled oceanic emissions of carbonyl sulfide and carbon disulfide for the period 2000-2019.
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- Earth System Science Data Discussions, 2020, p. 1, doi. 10.5194/essd-2020-389
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- Article
Long-term neuropsychological effects and MRI findings in patients with CS<sub>2</sub> poisoning.
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- Acta Neurologica Scandinavica, 2002, v. 106, n. 5, p. 269, doi. 10.1034/j.1600-0404.2002.01245.x
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Synthesis of some novel phenylfuro[3,2-d]pyrimidine glycosides derivatives with expected antimicrobial activity.
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- Journal of the Iranian Chemical Society, 2020, v. 17, n. 2, p. 319, doi. 10.1007/s13738-019-01768-2
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- Article
A facile approach for synthesis of thiazines-, thiazoles- and triazoles-annulated 6-styryl-2-thiouracil derivative.
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- Journal of the Iranian Chemical Society, 2020, v. 17, n. 1, p. 119, doi. 10.1007/s13738-019-01760-w
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Semi-automated continuous sample drop flow microextraction with swift preconcentration and atomic absorption spectrometry determination of lead in water and apple leaves.
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- Journal of the Iranian Chemical Society, 2018, v. 15, n. 11, p. 2511, doi. 10.1007/s13738-018-1439-3
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A facile and effective procedure for synthesis of polyfunctionalized pyrrolines from simultaneously stirring of carbon disulfide, aniline, arylglyoxals and β-enaminocarbonyls.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 11, p. 2299, doi. 10.1007/s13738-017-1166-1
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- Article
A one-pot synthesis of functionalized 4,5-bis(phenylimino)-1,3-thiazolidine-2-thiones from primary amines, CS and N, N'-diphenyloxalimidoyl dichloride.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 10, p. 1847, doi. 10.1007/s13738-016-0901-3
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An efficient synthesis of highly functionalized fluorenes and fluorenothiazines.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 2, p. 369, doi. 10.1007/s13738-015-0745-2
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- Article
A facile and efficient one-pot synthesis of 6-amino-2-oxo-4-aryl-4 H-1,3-dithiine-5-carbonitrile derivatives in water.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 11, p. 2051, doi. 10.1007/s13738-015-0681-1
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Three-component reaction between amines, carbon disulfide and electron-deficient derivatives of chloropyridine or chlorobenzene: synthesis of 3,6-diazaspiro[4.5]deca-2,7,9-trien-6-ium chloride and dithioylcarbamates derivatives.
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- Journal of the Iranian Chemical Society, 2014, v. 11, n. 2, p. 289, doi. 10.1007/s13738-013-0300-y
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Efficient synthesis of functionalized dithiocarbamate derivatives through one-pot three-component reaction and evaluation of their antimicrobial activities.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 4, p. 725, doi. 10.1007/s13738-012-0206-0
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- Article
Synthesis of oxoindolin-3-ylidene-1,3-dithioles.
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- Journal of the Iranian Chemical Society, 2012, v. 9, n. 3, p. 333, doi. 10.1007/s13738-011-0028-5
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- Article
A Novel One-Pot Synthesis of 2-Alkylthio-1,3,4-oxadiazoles in Water.
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- Journal of the Iranian Chemical Society, 2011, v. 8, n. 2, p. 525, doi. 10.1007/BF03249086
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- Article