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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
Journal Article
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
Journal Article
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
Journal Article
Chemistry - A European Journal, ISSN 0947-6539, 08/2015, Volume 21, Issue 35, pp. 12205 - 12205
Journal Article
Organic Process Research and Development, ISSN 1083-6160, 2017, Volume 21, Issue 1, pp. 79 - 84
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2016, Volume 55, Issue 39, pp. 11801 - 11805
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2017, Volume 56, Issue 17, pp. 4877 - 4881
Journal Article
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
Journal Article
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
Journal Article
Angewandte Chemie, ISSN 0044-8249, 04/2017, Volume 129, Issue 17, pp. 4704 - 4704
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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... 
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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