Works matching DE "SULFONYL compounds"
Results: 274
A fast and simple approach to the quantitative evaluation of fibrinogen coagulation.
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- Biotechnology Letters, 2014, v. 36, n. 2, p. 337, doi. 10.1007/s10529-013-1365-5
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Chemospecific reactions of as-triazine ring reduction in sulfonyl derivatives of pyrazolo[5,1- c][1,2,4]triazines.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1128, doi. 10.1007/s10593-017-2183-9
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Acid-catalyzed reaction of phenols with N-(4,4-diethoxybutyl)sulfonamides - a new method for the synthesis of 2-aryl-1-sulfonylpyrrolidines.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 2, p. 161, doi. 10.1007/s10593-017-2034-8
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Development of Abraham model IL-specific correlations for N-triethyl(octyl)ammonium bis(fluorosulfonyl)imide and 1-butyl-3-methylpyrrolidinium bis(fluorosulfonyl)imide.
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- Physics & Chemistry of Liquids, 2019, v. 57, n. 6, p. 733, doi. 10.1080/00319104.2018.1519713
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Saturated and compressed liquid heat capacity at constant volume for 1-hexyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide).
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- Physics & Chemistry of Liquids, 2014, v. 52, n. 5, p. 657, doi. 10.1080/00319104.2014.924381
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Some Aryl Sulfonyl Ester-Based Heterocyclic Schiff Bases: Synthesis, Structure Elucidation and Antioxidant Activity.
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- Journal of the Institute of Science & Technology / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2021, v. 11, n. 4, p. 2967, doi. 10.21597/jist.963129
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Some Aryl Sulfonyl Ester-Based Heterocyclic Schiff Bases: Synthesis, Structure Elucidation and Antioxidant Activity.
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- Journal of the Institute of Science & Technology / Iğdır Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2021, v. 11, n. 4, p. 3967, doi. 10.21597/jist.963129
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One-pot synthesis of sulfonylhydrazones from sulfonyl chloride, hydrazine hydrate and vinyl azide in water.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 10, p. 2713, doi. 10.1007/s13738-021-02226-8
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A surfactant-heme-sulfonyl imidazole system as a nano-artificial enzyme.
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- Journal of the Iranian Chemical Society, 2013, v. 10, n. 5, p. 961, doi. 10.1007/s13738-013-0233-5
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Sulfonylation of aromatic compounds with methyl p-toluenesulfonate as a sulfonylating precursor.
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- Journal of the Iranian Chemical Society, 2012, v. 9, n. 4, p. 507, doi. 10.1007/s13738-011-0062-3
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Self‐Promoted Glycosylation for the Synthesis of β‐N‐Glycosyl Sulfonyl Amides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 41, p. 5685, doi. 10.1002/ejoc.202100808
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Temperature‐Controlled Chemoselective Synthesis of Thiosulfonates and Thiocyanates: Novel Reactivity of KXCN (X=S, Se) towards Organosulfonyl Chlorides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 38, p. 5359, doi. 10.1002/ejoc.202101031
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Recent Advances in the Synthesis of Sulfonylureas.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 8, p. 1201, doi. 10.1002/ejoc.202001437
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Iodine-Mediated Coupling of Cyclic Amines with Sulfonyl Hydrazides: an Efficient Synthesis of Vinyl Sulfone Derivatives.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 4, p. 701, doi. 10.1002/ejoc.202001510
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Amino Acid‐Based Dithiocarbamates as Efficient Intermediates for Diversity‐Oriented Synthesis of Thiazoles.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 38, p. 6081, doi. 10.1002/ejoc.202001050
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Recent Advances in Sulfur‐Centered S–X (X = N, P, O) Bond Formation Catalyzed by Transition Metals.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 34, p. 5488, doi. 10.1002/ejoc.202000541
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Iodine‐Catalyzed Ring Opening of 1,1‐Diacylcyclopropanes for Synthesis of Fully Substituted Pyrazole Derivatives.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 25, p. 3856, doi. 10.1002/ejoc.202000496
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Synthesis of Sulfonyl Fluorides from Sulfonamides.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 17, p. 2497, doi. 10.1002/ejoc.202000022
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3‐Carboxy‐/3‐Aminobicyclo[1.1.1]pentane‐Derived Sulfonamides and Sulfonyl Fluorides – Advanced Bifunctional Reagents for Organic Synthesis and Drug Discovery.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 15, p. 2210, doi. 10.1002/ejoc.202000303
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I<sub>2</sub>‐Catalyzed N‐Sulfonylation of Sulfoximines with Sulfinates in Water at Room Temperature.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 11, p. 1764, doi. 10.1002/ejoc.202000120
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Synthesis of N‐Sulfonyl Pyrazoles Through Cyclization Reactions of Sulfonyl Hydrazines with Enaminones Promoted by p‐TSA.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 9, p. 1154, doi. 10.1002/ejoc.201901886
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B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>‐Catalyzed Reduction of Cyclic N‐Sulfonyl Ketimines.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 38, p. 6550, doi. 10.1002/ejoc.201900706
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Regioselective Thermal [3+2]‐Dipolar Cycloadditions of α‐Diazoacetates with α‐Sulfenyl/Sulfinyl/Sulfonyl‐β‐Chloroacrylamide Derivatives to Form Densely Functionalised Pyrazoles.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5368, doi. 10.1002/ejoc.201900494
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Pd/Zn(OTf)<sub>2</sub> Co‐Catalyzed Asymmetric Hydrogenation of Imines under Normal Pressure of Hydrogen.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 45, p. 6274, doi. 10.1002/ejoc.201801123
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α‐Amino Acid Sulfonamides as Versatile Sulfonylation Reagents: Silver‐Catalyzed Synthesis of Coumarins and Oxindoles by Radical Cyclization.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 43, p. 5905, doi. 10.1002/ejoc.201800901
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Synthesis of 3‐Amino‐1‐benzothiophene‐1,1‐diones by Alkyne Directed Hydroarylation and 1/N→3/C‐Sulfonyl Migration.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 39, p. 5435, doi. 10.1002/ejoc.201801062
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Thermal Ring Expansion of 2‐Sulfonylimidoyl‐1‐phthalimidoaziridines into <italic>N</italic>‐Sulfonylimidazoles.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 14, p. 1634, doi. 10.1002/ejoc.201701806
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Hydroxysulfonylation of Quinones with Aryl(alkyl)sulfonyl Hydrazides for the Synthesis of 1,4-Dihydroxy-2-aryl(alkyl)sulfonylbenzenes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 40, p. 6081, doi. 10.1002/ejoc.201701199
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Enantiomeric Catalytic Formal Thiolation of 2,5-Dimethyl-3-[1-(arylsulfonyl)alkyl]pyrroles in an Oil/Water Biphasic System.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 35, p. 5826, doi. 10.1002/ejoc.201601180
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A Click Ligation Based on SuFEx for the Metal-Free Synthesis of Sugar and Iminosugar Clusters.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 30, p. 5102, doi. 10.1002/ejoc.201600732
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Silver-Catalyzed Denitrative Sulfonylation of β-Nitrostyrenes: A Convenient Approach to (E)-Vinyl Sulfones.
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- European Journal of Organic Chemistry, 2016, p. 2695, doi. 10.1002/ejoc.201600237
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Direct Synthesis of Enolizable N-Sulfonyl Ketimines Under Microwave Irradiation.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 7, p. 1247, doi. 10.1002/ejoc.201600022
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Tunable Titanocene Lewis Acid Catalysts for Selective Friedel-Crafts Reaction of Indoles and N-Sulfonylaldimines.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 3, p. 502, doi. 10.1002/ejoc.201501122
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Copper-Catalyzed Synthesis of N-Formyl/Acylsulfenamides and -thiosulfonamides.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 27, p. 5934, doi. 10.1002/ejoc.201500857
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Asymmetric Synthesis of δ-Chloro-β-amino- N-sulfinyl Imidates as Versatile Chiral Building Blocks for the Synthesis of 2,3-Disubstituted Piperidines.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 22, p. 4847, doi. 10.1002/ejoc.201500466
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Asymmetric Enynylation of N-Sulfonyl Aldimines Catalyzed by Zn-BINOL Complexes.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 18, p. 3905, doi. 10.1002/ejoc.201500400
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Generation of Sulfonyl Radicals from Aryldiazonium Tetrafluoroborates and Sulfur Dioxide: The Synthesis of 3-Sulfonated Coumarins.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 39, p. 11925, doi. 10.1002/anie.201607292
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Gold(I)-Catalyzed N-Desulfonylative Amination versus N-to-O 1,5-Sulfonyl Migration: A Versatile Approach to 1-Azabicycloalkanes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 31, p. 9088, doi. 10.1002/anie.201604329
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A syn-Selective Aza-Aldol Reaction of Boron Aza-Enolates Generated from N-Sulfonyl-1,2,3-Triazoles and 9-BBN-H.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 30, p. 8732, doi. 10.1002/anie.201603270
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Kinetic Resolution of β-Sulfonyl Ketones through Enantioselective β-Elimination using a Cation-Binding Polyether Catalyst.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 1, p. 331, doi. 10.1002/anie.201508127
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N-Heterocyclic Carbene Catalyzed Synthesis of δ-Sultones via α,β-Unsaturated Sulfonyl Azolium Intermediates.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 40, p. 11780, doi. 10.1002/anie.201504633
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The Methylsulfonyloxyl Radical, CH<sub>3</sub>SO<sub>3</sub>.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 39, p. 11404, doi. 10.1002/anie.201503776
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Crystal structure of methyl (E)-N<sup>2</sup>-((3-methylquinolin-8-yl)sulfonyl)-N<sup>ω</sup>′-nitro-L-argininate - ethanol (1/1), C<sub>19</sub>H<sub>28</sub>N<sub>6</sub>O<sub>7</sub>S.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2020, v. 235, n. 2, p. 275, doi. 10.1515/ncrs-2019-0597
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Frontmatter.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2019, v. 234, n. 6, p. i, doi. 10.1515/ncrs-2019-frontmatter4
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Crystal structure of poly-[(μ<sub>2</sub>-(carboxylatomethyl)((3-nitrophenyl)sulfonyl)amido-κ³N:O:O′)(μ<sub>2</sub>-4,4′-bipyridine-κ²N:N′) nickel(II)], C<sub>18</sub>H<sub>14</sub>NiN<sub>4</sub>O<sub>6</sub>S.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2019, v. 234, n. 3, p. 549, doi. 10.1515/ncrs-2018-0551
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Crystal structure of N-(5-((3,5-dimethylisoxazol-4-yl)sulfonyl)quinolin-8-yl)benzamide, C<sub>21</sub>H<sub>17</sub>N<sub>3</sub>O<sub>4</sub>S.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 4, p. 1189, doi. 10.1515/ncrs-2016-0127
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Crystal structure of poly-[μ-1,4-bis(2-ethylbenzimidazol-1-ylmethyl)benzene-κ<sup>2</sup> N: N′)-bis(μ<sub>4</sub>-4,4′-sulfonyldibenzoato-κ<sup>4</sup> O: O′: O′′: O′′′)dicadmium(II)] monohydrate, C<sub>52</sub>H<sub>42</sub>N<sub>4</sub>O<sub>14</sub>Cd<sub>2</sub>
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 3, p. 951, doi. 10.1515/ncrs-2016-0018
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Crystal structure of trans-tetraaquabis(4-(pyridin-4-ylsulfonyl)pyridine-κ N)cobalt(II) diperchlorate dihydrate, C<sub>20</sub>H<sub>28</sub>Cl<sub>2</sub>CoN<sub>4</sub>O<sub>18</sub>S<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 1, p. 277, doi. 10.1515/ncrs-2015-0119
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Crystal structure of trans-tetraaqua-bis(4,4′-sulfonyldipyridine-κ N)zinc(II) diperchlorate dihydrate, C<sub>20</sub>H<sub>28</sub>Cl<sub>2</sub>ZnN<sub>4</sub>O<sub>18</sub>S<sub>2</sub>.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2016, v. 231, n. 1, p. 293, doi. 10.1515/ncrs-2015-0128
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Crystal structure of 4,4'-sulfonyldipyridine - 3-chlorobenzoic acid (1:1), C<sub>24</sub>H<sub>18</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>6</sub>S.
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- Zeitschrift für Kristallographie / New Crystal Structures, 2014, v. 229, n. 4, p. 301, doi. 10.1515/ncrs-2014-0152
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