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1. Full Text Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent‐ and Metal‐Free Anodic Cross‐Coupling Reaction
by Wiebe, Anton and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2016, Volume 55, Issue 39, pp. 11801 - 11805
C–C coupling | C–H activation | protecting groups | biaryls | electrochemistry | Chemical tests and reagents | Electrochemistry | Electrochemical reactions
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2. Full Text Reagent‐ and Metal‐Free Anodic C−C Cross‐Coupling of Aniline Derivatives
by Schulz, Lara and Enders, Mathias and Elsler, Bernd and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2017, Volume 56, Issue 17, pp. 4877 - 4881
cross-coupling | protecting groups | C−H activation | biaryls | electrochemistry | Electrochemistry | Electrochemical reactions | Aniline | Chemical tests and reagents | Organic acids | Carbon-carbon composites | Cross coupling | Dehydrogenation | Metals | Protecting groups | Reagents | Oxidation | Carboxylic acids | High temperature | Derivatives | Glassy carbon
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3. Full Text Synthesis of meta‐Terphenyl‐2,2′′‐diols by Anodic C−C Cross‐Coupling Reactions
by Lips, Sebastian and Wiebe, Anton and Elsler, Bernd and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2016, Volume 55, Issue 36, pp. 10872 - 10876
meta-terphenyl compounds | protecting groups | pincer ligands | C−C coupling | electrochemistry | Carbon-carbon composites | Coupling (molecular) | Cross coupling | Electrolysis | Phenols | Electrochemistry | Chemical reactions | Selectivity | Chemical synthesis | Functional groups | Diols
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4. Full Text Electro-organic Synthesis as a Sustainable Alternative for Dehydrogenative Cross-Coupling of Phenols and Naphthols
by Riehl, Barbara and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Synthesis (Stuttgart), ISSN 0039-7881, 01/2017, Volume 49, Issue 2, pp. 252 - 259
feature | electrolysis | phenols | anodic oxidation | cross-coupling | naphthols | biphenols | dehydrogenative coupling
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5. Full Text Cover Picture: Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent‐ and Metal‐Free Anodic Cross‐Coupling Reaction (Angew. Chem. Int. Ed. 39/2016)
by Wiebe, Anton and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2016, Volume 55, Issue 39, pp. 11689 - 11689
C–C coupling | C–H activation | protecting groups | biaryls | electrochemistry
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6. Full Text Inside Cover: Reagent‐ and Metal‐Free Anodic C−C Cross‐Coupling of Aniline Derivatives (Angew. Chem. Int. Ed. 17/2017)
by Schulz, Lara and Enders, Mathias and Elsler, Bernd and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2017, Volume 56, Issue 17, pp. 4632 - 4632
cross-coupling | protecting groups | C−H activation | biaryls | electrochemistry | Carbon-carbon composites | Cross coupling | Anodic protection | Aniline | Workers | Protecting groups | Electrochemistry | Selectivity | Propanol | Derivatives | Polyanilines | Carbonyls
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7. Full Text Facile and Selective Cross‐Coupling of Phenols Using Selenium Dioxide
by Quell, Thomas and Beiser, Nicole and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
European journal of organic chemistry, ISSN 1434-193X, 09/2016, Volume 2016, Issue 25, pp. 4307 - 4310
C–C coupling | Arenes | Synthetic methods | Oxidation | Selenium | Biaryls | Selenium compounds | Phenols | Bisphenol-A
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8. Full Text Metal‐ and Reagent‐Free Highly Selective Anodic Cross‐Coupling Reaction of Phenols
by Elsler, Bernd and Schollmeyer, Dieter and Dyballa, Katrin Marie and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2014, Volume 53, Issue 20, pp. 5210 - 5213
oxidative coupling | anodic biaryl synthesis | green chemistry | phenol cross‐coupling | CC coupling | C-C coupling | phenol cross-coupling | Electrodes | Phenols - chemistry | Metals - chemistry | Indicators and Reagents - chemistry | Electrolysis | Chemical tests and reagents | Metal catalysts | Hydrogen | Formic acid | Green technology | Phenols | Green chemistry | Telomerase | Organic acids | Chemical industry | Index Medicus | Electrolytic cells | Solvents | Catalysts | Methyl alcohol | Transformations | Selectivity | Catalysis
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9. Full Text Metal-catalyzed carbonylation of alkynes: key aspects and recent development
by Quintero-Duque, Samuel and Dyballa, Katrin Marie and Fleischer, Ivana
Tetrahedron letters, ISSN 0040-4039, 05/2015, Volume 56, Issue 21, pp. 2634 - 2650
Pauson–Khand reaction | Carbonylation | Hydroesterification | Homogeneous catalysis | Alkynes | Homogeneous catalysis Carbonylation Alkynes Hydroesterification Pauson-Khand reaction | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
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10. Full Text Source of Selectivity in Oxidative Cross‐Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol
by Elsler, Bernd and Wiebe, Anton and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Chemistry : a European journal, ISSN 0947-6539, 08/2015, Volume 21, Issue 35, pp. 12321 - 12325
electrolysis | solvent effects | biaryls | cross‐coupling | hydrogen bonds | cross-coupling | Aniline | Electrolysis | Hydrogen | Phenols | Oxidation | Solvent effect | Solvents | Cross coupling | Decoupling | Selectivity | Electrode potentials
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11. Full Text Solvent‐Dependent Facile Synthesis of Diaryl Selenides and Biphenols Employing Selenium Dioxide
by Quell, Thomas and Mirion, Michael and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
ChemistryOpen (Weinheim), ISSN 2191-1363, 04/2016, Volume 5, Issue 2, pp. 115 - 119
oxidation | catalysis | C−C coupling | arenes | biaryls | selenium dioxide | C-C coupling | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Selenium compounds | Pyridine | Selenium | Catalysis | Transition metal compounds | Organic acids | Ligands | Solvents | Temperature | Transition metals | Dioxides | Molecular structure | Selenides | Selenium dioxide | Acids | Phenols | Acetic acid | Conversion | Oxidizers
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12. Full Text Supported homogeneous catalyst makes its own liquid phase
by Kaftan, Andre and Schönweiz, Andreas and Nikiforidis, Ioannis and Hieringer, Wolfgang and Dyballa, Katrin M and Franke, Robert and Görling, Andreas and Libuda, Jörg and Wasserscheid, Peter and Laurin, Mathias and Haumann, Marco
Journal of catalysis, ISSN 0021-9517, 01/2015, Volume 321, pp. 32 - 38
Infrared spectroscopy | Supported homogeneous catalysis | Rhodium | Hydroformylation | Density functional theory | Silicon dioxide | Operando spectroscopy | Engineering | Physical Sciences | Engineering, Chemical | Chemistry | Technology | Chemistry, Physical | Science & Technology | Kinetics | Catalysis | Catalysts
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