0000000000072975

AUTHOR

Timo Müller

showing 12 related works from this author

Aktive Anode auf Molybdänbasis für dehydrierende Kupplungen

2018

010405 organic chemistryChemistryGeneral Medicine010402 general chemistry01 natural sciences0104 chemical sciencesAngewandte Chemie
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About the selectivity and reactivity of active nickel electrodes in C–C coupling reactions

2020

Active anodes which are operating in highly stable protic media such as 1,1,1,3,3,3-hexafluoroisopropanol are rare. Nickel forms, within this unique solvent, a non-sacrificial active anode at constant current conditions, which is superior to the reported powerful molybdenum system. The reactivity for dehydrogenative coupling reactions of this novel active anode increases when the electrolyte is not stirred during electrolysis. Besides the aryl-aryl coupling, a dehydrogenative arylation reaction of benzylic nitriles was found while stirring the mixture providing quick access to synthetically useful building blocks.

ElectrolysisChemistryGeneral Chemical Engineeringchemistry.chemical_elementGeneral ChemistryElectrolyteCombinatorial chemistryCoupling reactionAnodelaw.inventionSolventNickellawReactivity (chemistry)SelectivityRSC Advances
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Investigations on isomerization and rearrangement of polycyclic arenes under oxidative conditions – Anodic versus reagent-mediated reactions

2019

Abstract Electro-organic conversions at an active molybdenum anode enable the formation of fused arenes. High chemoselectivity was achieved under anodic conditions, and a reagent-induced selectivity was observed by comparison with results of MoCl5-mediated reactions. Polycyclic arenes like phenanthrenes, triphenylenes, chrysenes, or helicenes were selectively obtained in yields up to 87% and in some cases unusual rearrangements were crucial for the product formation.

General Chemical Engineeringchemistry.chemical_elementOxidative couplingRearrangement02 engineering and technologyOxidative phosphorylation010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesElectrolysis0104 chemical sciencesAnodeAnodechemistryMolybdenumReagentElectrochemistryPhenanthrenesChemoselectivityPolycyclic arenes0210 nano-technologySelectivityIsomerizationElectrochimica Acta
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Mild, Fast, and Easy To Conduct MoCl5-Mediated Dehydrogenative Coupling Reactions in Flow

2018

A convenient and straightforward approach to performing oxidative coupling reactions in flow is presented. A collection of electron-rich benzene derivatives was subjected to this protocol, and the distinct utility of molybdenum pentachloride (MoCl5) is established. Using this unexplored protocol, biphenyls could be obtained in 21–91% isolated yield. This simple protocol opens a new chapter in reagent-mediated dehydrogenative coupling reactions, and yields are compared to classical approaches.

010405 organic chemistryChemistryOrganic ChemistryMolybdenum pentachloride010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistryCoupling reaction0104 chemical sciencesFlow (mathematics)Yield (chemistry)Benzene derivativesOxidative coupling of methanePhysical and Theoretical ChemistryOrganic Letters
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Active Molybdenum‐Based Anode for Dehydrogenative Coupling Reactions

2018

A new and powerful active anode system that can be operated in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) has been discovered. In HFIP the molybdenum anode forms a compact, conductive, and electroactive layer of higher-valent molybdenum species. This system can replace powerful but stoichiometrically required MoV reagents for the dehydrogenative coupling of aryls. This electrolytic reaction is more sustainable and allows the conversion of a broad scope of activated arenes.

Materials science010405 organic chemistrychemistry.chemical_elementGeneral ChemistryElectrolyte010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reaction0104 chemical sciencesAnodechemistryMolybdenumReagentOxidative coupling of methaneStoichiometryAngewandte Chemie International Edition
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CCDC 1882077: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters2367-tetramethoxy-1-phenyltriphenyleneExperimental 3D Coordinates
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CCDC 1882075: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters3-(34-dimethoxyphenyl)-171011-tetramethoxytriphenylene dichloromethane solvateExperimental 3D Coordinates
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CCDC 1882076: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

914-bis(ethoxycarbonyl)-2367-tetramethoxy[5]heliceneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1882073: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

diethyl 2351011-pentamethoxybenzo[c]chrysene-814-dicarboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1976461: Experimental Crystal Structure Determination

2020

Related Article: Sebastian B. Beil, Manuel Breiner, Lara Schulz, Aaron Schüll, Timo Müller, Dieter Schollmeyer, Alexander Bomm, Michael Holtkamp, Uwe Karst, Wolfgang Schade, Siegfried R. Waldvogel|2020|RSC Advances|10|14249|doi:10.1039/D0RA02673E

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(3-bromo-4-methoxyphenyl)(34-dimethoxyphenyl)acetonitrile methanol solvateExperimental 3D Coordinates
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CCDC 1882074: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersdiethyl 6789-tetramethoxybenzo[ghi]perylene-411-dicarboxylate dichloromethane solvateExperimental 3D Coordinates
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CCDC 1882078: Experimental Crystal Structure Determination

2019

Related Article: Sebastian B. Beil, Peter Franzmann, Timo Müller, Maximilian M. Hielscher, Tobias Prenzel, Dennis Pollok, Nicole Beiser, Dieter Schollmeyer, Siegfried R. Waldvogel|2018|Electrochimica Acta|302|310|doi:10.1016/j.electacta.2019.02.041

23561011-hexamethoxy-8-methylbenzo[e]acephenanthryleneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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