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1. 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 Edition, ISSN 1433-7851, 09/2016, Volume 55, Issue 39, pp. 11689 - 11689
Rotation about the biaryl axis leads to higher yield and selectivity in the electrochemical cross‐coupling giving partially protected 2,2′‐biphenols. In their... 
C–C coupling | C–H activation | protecting groups | biaryls | electrochemistry
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2. 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 Edition, ISSN 1433-7851, 04/2017, Volume 56, Issue 17, pp. 4632 - 4632
The formation of polyanilines is avoided in an anodic coupling of anilines with simple and easily removable carbonyl‐based protecting groups. In their... 
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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3. 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. 12209 - 12209
Invited for the cover of this issue is the group of Siegfried R. Waldvogel at the Johannes Gutenberg‐Universität Mainz (Germany). The image depicts a monkey... 
Solvent effect | Solvents | Decoupling | Methyl alcohol | Texts | Monkeys | Electrode potentials | Tuning
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4. Full Text Cover Picture: Source of Selectivity in Oxidative Cross-Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3-Hexafluoropropan-2-ol (Chem. Eur. J. 35/2015)
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. 12205 - 12205
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5. Full Text Scalable and selective preparation of 3,3',5,5'-tetramethyl-2,2'-biphenol
by Quell, Thomas and Hecken, Nadine and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Organic Process Research and Development, ISSN 1083-6160, 2017, Volume 21, Issue 1, pp. 79 - 84
Biphenols are indispensable building blocks in ligand systems for organic catalysis. 3,3'5,5'-Tetramethyl-2,2'-biphenol is a particular versatile motif in... 
Selenium dioxide | C H activation | Oxidation | Phenol-phenol coupling | Scalable | Biphenol | scalable | BINOL | PHENOL-COUPLING REACTION | ADIPIC ALDEHYDE | NATURAL-PRODUCTS | oxidation | CHEMISTRY, ORGANIC | biphenol | TROPOS PHOSPHORUS LIGANDS | QUATERNARY CENTERS | LIQUID-CRYSTALLINE POLYMERS | phenol-phenol coupling | CATALYZED CONJUGATE ADDITION | CHEMISTRY, APPLIED | selenium dioxide | DYNAMIC LIBRARY | C,H activation | HYDROFORMYLATION
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6. 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 Edition, ISSN 1433-7851, 09/2016, Volume 55, Issue 39, pp. 11801 - 11805
The oxidative cross‐coupling of aromatic substrates without the necessity of leaving groups or catalysts is described. The selective formation of partially... 
C–C coupling | C–H activation | protecting groups | biaryls | electrochemistry | C-C coupling | OXIDATION | NOBEL LECTURE | 2,4-DIMETHYLPHENOL | UNSYMMETRICAL BIPHENOLS | NATURAL-PRODUCTS | STRATEGY | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | C-H activation | PHENOLS | 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL | HIGHLY FLUORINATED 2,2'-BIPHENOLS | Chemical tests and reagents | Electrochemistry | Electrochemical reactions
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7. 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 Edition, ISSN 1433-7851, 04/2017, Volume 56, Issue 17, pp. 4877 - 4881
The dehydrogenative cross‐coupling of aniline derivatives to 2,2′‐diaminobiaryls is reported. The oxidation is carried out electrochemically, which avoids the... 
cross-coupling | protecting groups | C−H activation | biaryls | electrochemistry | HYDRAZIDES | UNSYMMETRICAL BIPHENOLS | COMPLEXES | ARYLATION | BOND FORMATION | CHEMISTRY, MULTIDISCIPLINARY | C-H activation | PHENOLS | 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL | REARRANGEMENT REACTIONS | EFFICIENT | CATALYSTS | 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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8. 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 Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 36, pp. 10872 - 10876
The anodic C−C cross‐coupling reaction is a versatile synthetic approach to symmetric and non‐symmetric biphenols and arylated phenols. We herein present a... 
terphenyl compounds | protecting groups | pincer ligands | C−C coupling | electrochemistry | meta | meta-terphenyl compounds | C-C coupling | ALKYLIDENE | PINCER-TYPE LIGAND | 2,4-DIMETHYLPHENOL | COMPLEXES | COORDINATION | PHENOL-ARENE | CHEMISTRY, MULTIDISCIPLINARY | SIGMA-BOND METATHESIS | TRIANIONIC PINCER | 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL | INTERMEDIATE | Carbon-carbon composites | Coupling (molecular) | Cross coupling | Electrolysis | Phenols | Electrochemistry | Chemical reactions | Selectivity | Chemical synthesis | Functional groups | Diols
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9. 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
Solvents such as 1,1,1,3,3,3‐hexafluoroisopropanol (HFIP) with a high capacity for donating hydrogen bonds generate solvates that enter into selective... 
electrolysis | solvent effects | biaryls | cross‐coupling | hydrogen bonds | cross-coupling | ELECTROSYNTHESIS | HEXAFLUOROISOPROPANOL | NUCLEOPHILICITIES | RADICAL CATIONS | ELECTRODES | CHEMISTRY, MULTIDISCIPLINARY | BORON-DOPED DIAMOND | PHENOLS | FLUORINATED ALCOHOLS | WATER | Aniline | Electrolysis | Hydrogen | Phenols | Oxidation | Solvent effect | Solvents | Cross coupling | Decoupling | Selectivity | Electrode potentials
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10. 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, ISSN 0039-7881, 01/2017, Volume 49, Issue 2, pp. 252 - 259
Abstract The dehydrogenative cross-coupling of phenols and naphthols can be achieved by several oxidative methods. However, the key is the use of fluorinated... 
feature | electrolysis | phenols | anodic oxidation | cross-coupling | naphthols | biphenols | dehydrogenative coupling | ELECTROSYNTHESIS | 2,4-DIMETHYLPHENOL | ELECTRODES | CHEMISTRY, ORGANIC | DIRECT ANODIC-OXIDATION | BIARYL NATURAL-PRODUCTS | BORON-DOPED DIAMOND | RING-CLOSING METATHESIS | 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL | CHEMISTRY
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11. Full Text Innentitelbild: Reagens- und metallfreie anodische C-C-Kreuzkupplung von Anilinderivaten (Angew. Chem. 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, ISSN 0044-8249, 04/2017, Volume 129, Issue 17, pp. 4704 - 4704
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12. Full Text Reagens‐ und metallfreie anodische C‐C‐Kreuzkupplung von Anilinderivaten
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, ISSN 0044-8249, 04/2017, Volume 129, Issue 17, pp. 4955 - 4959
Vorgestellt wird die oxidative Kreuzkupplung von Anilinderivaten zu 2,2′‐Diaminobiarylen. Der Oxidationsschritt wird elektrochemisch durchgeführt, ohne die... 
Schutzgruppen | Elektrochemie | Kreuzkupplungen | Biaryle | C-H-Aktivierung
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13. Full Text Innentitelbild: Reagens‐ und metallfreie anodische C‐C‐Kreuzkupplung von Anilinderivaten (Angew. Chem. 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, ISSN 0044-8249, 04/2017, Volume 129, Issue 17, pp. 4704 - 4704
Die Bildung von Polyanilinen lässt sich durch anodische Kupplung von Anilinen mit einfachen carbonylbasierten und leicht entfernbaren Schutzgruppen vermeiden.... 
Schutzgruppen | Elektrochemie | Kreuzkupplungen | Biaryle | C-H-Aktivierung
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14. Full Text Reagens- und metallfreie anodische C-C-Kreuzkupplung von Anilinderivaten
by Lara Schulz and Mathias Enders and Bernd Elsler and Dieter Schollmeyer and Katrin M Dyballa and Robert Franke and Siegfried R Waldvogel
Angewandte Chemie, ISSN 0044-8249, 04/2017, Volume 129, Issue 17, p. 4955
  Vorgestellt wird die oxidative Kreuzkupplung von Anilinderivaten zu 2,2'-Diaminobiarylen. Der Oxidationsschritt wird elektrochemisch durchgefuhrt, ohne die... 
Carbon-carbon composites
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15. Full Text Innentitelbild: Reagens- und metallfreie anodische C-C-Kreuzkupplung von Anilinderivaten
by Lara Schulz and Mathias Enders and Bernd Elsler and Dieter Schollmeyer and Katrin M Dyballa and Robert Franke and Siegfried R Waldvogel
Angewandte Chemie, ISSN 0044-8249, 04/2017, Volume 129, Issue 17, p. 4704
  Die Bildung von Polyanilinen lässt sich durch anodische Kupplung von Anilinen mit einfachen carbonylbasierten und leicht entfernbaren Schutzgruppen... 
Carbon-carbon composites | Propanol | Carbonyls
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16. Full Text Selektive Synthese teilgeschutzter unsymmetrischer Biphenole durch reagens- und metallfreie anodische Kreuzkupplung
by Anton Wiebe and Dieter Schollmeyer and Katrin M Dyballa and Robert Franke and Siegfried R Waldvogel
Angewandte Chemie, ISSN 0044-8249, 09/2016, Volume 128, Issue 39, p. 11979
  Vorgestellt wird die oxidative Kreuzkupplung von Arenen ohne Abgangsfunktionalitäten oder Katalysatoren. Die selektive Synthese teilgeschutzter... 
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17. Full Text Synthese von meta-Terphenyl-2,2''-diolen durch anodische C-C-Kreuzkupplungen
by Sebastian Lips and Anton Wiebe and Bernd Elsler and Dieter Schollmeyer and Katrin M Dyballa and Robert Franke and Siegfried R Waldvogel
Angewandte Chemie, ISSN 0044-8249, 08/2016, Volume 128, Issue 36, p. 11031
  Die anodische C-C-Kreuzkupplung ist eine vielseitig einsetzbare Transformation, die eine gezielte Synthese von Biphenolen und arylierten Phenolen ermöglicht.... 
Carbon-carbon composites | Transformation
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18. 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
Nonsymmetric biphenols are important structural motifs in organic chemistry. Therefore, an easy and versatile protocol for oxidative cross‐coupling is... 
C–C coupling | Arenes | Synthetic methods | Oxidation | Selenium | Biaryls | C-C coupling | BINOL | ACTIVATION | UNSYMMETRICAL BIPHENOLS | COMPLEXES | CHEMISTRY, ORGANIC | LIQUID-CRYSTALLINE POLYMERS | BIARYL NATURAL-PRODUCTS | 2-NAPHTHOLS | 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL | METAL | FLUORINATED ALCOHOLS | Selenium compounds | Phenols | Bisphenol-A
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19. Full Text Titelbild: Selektive Synthese teilgeschützter unsymmetrischer Biphenole durch reagens‐ und metallfreie anodische Kreuzkupplung (Angew. Chem. 39/2016)
by Wiebe, Anton and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie, ISSN 0044-8249, 09/2016, Volume 128, Issue 39, pp. 11863 - 11863
Die Verdrillung der Biarylachse wie bei einem Wagenrad führt zu höheren Ausbeuten und Selektivitäten bei der elektrochemischen Kreuzkupplung zu partiell... 
Schutzgruppen | Elektrochemie | C-C-Kupplungen | Biaryle | C-H-Aktivierung
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20. 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
A catalyst designed for homogeneous catalysis is shown to generate its own liquid phase if deposited onto a support. In this way, a macroscopically... 
Infrared spectroscopy | Supported homogeneous catalysis | Rhodium | Hydroformylation | Density functional theory | Silicon dioxide | Operando spectroscopy | APPROXIMATION | PERFORMANCE | 1-DODECENE | PROPENE | CHEMISTRY, PHYSICAL | ENGINEERING, CHEMICAL | ALKENES | BUTENE-1 | BASIS-SETS | MODIFIED RHODIUM CATALYSTS | PROGRAM | Chemistry | Kinetics | Catalysis | Catalysts
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