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Chemistry (Weinheim an der Bergstrasse, Germany), ISSN 0947-6539, 12/2019
Ruthenium(II) alkylidene complexes such as the Grubbs' 1st and 2nd generation catalysts undergo a ligand substitution with 2,2'-bypyridine, which readily leads... 
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2017, Volume 56, Issue 35, pp. 10280 - 10281
Donation welcome: Recent developments in visible‐light photocatalysis allow the utilization of increasingly negative reduction potentials. Successive energy... 
sensitization | radicals | photocatalysis | polycyclic aromatic hydrocarbons | reduction | HALIDES | ORGANIC-SYNTHESIS | ACTIVATION | COSENSITIZATION | CONVERSION | COMPLEXES | DONORS | AGENTS | CHEMISTRY, MULTIDISCIPLINARY | TRANSFORMATIONS | PHOTOREDOX CATALYSIS | Polycyclic aromatic hydrocarbons | Electron transport | Catalysis | Reduction | Anions | Energy use | Energy | Photocatalysis | Reagents | Electron transfer
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 5, pp. 1402 - 1406
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2017, Volume 129, Issue 35, pp. 10414 - 10415
Weniger ist mehr: Aktuelle Entwicklungen in der Photokatalyse machen zunehmend negative Reduktionspotentiale synthetisch nutzbar. Feinabgestimmte Energie‐ und... 
Sensibilisierung | Photokatalyse | Polycyclische aromatische Kohlenwasserstoffe | Radikale | Reduktion
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2017, Volume 129, Issue 35, pp. 10414 - 10415
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2017, Volume 129, Issue 35, p. 10414
Weniger ist mehr: Aktuelle Entwicklungen in der Photokatalyse machen zunehmend negative Reduktionspotentiale synthetisch nutzbar. Feinabgestimmte Energie- und... 
Journal Article
Chemical Communications, ISSN 1359-7345, 2016, Volume 52, Issue 5, pp. 1025 - 1028
Common photoredox catalysts Ru(bpy)32+ and Ru(bpz)32+ are rapidly converted into Ruthenium(viii)-oxide through continuous visible light irradiation in the... 
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2014, Volume 53, Issue 25, pp. 6558 - 6562
Quinones exhibit orthogonal ground‐ and excited‐state reactivities and are therefore highly suitable organocatalysts for the development of sequential... 
organocatalysis | indoles | quinones | photocatalysis | tandem catalysis | Quinone | Catalysis | Quinones | Amines | Catalysts | Anthraquinones | Indoles | Derivatives | Photooxidation | Alkylation
Journal Article
ISSN 1359-7345, 1/2016, Volume 52, Issue 5, pp. 125 - 128
Common photoredox catalysts Ru(bpy) 3 2+ and Ru(bpz) 3 2+ are rapidly converted into Ruthenium( viii )-oxide through continuous visible light irradiation in... 
Journal Article
ChemCatChem, ISSN 1867-3880, 09/2016, Volume 8, Issue 18, pp. 2881 - 2884
Photocatalytic aerobic benzylic C(sp3)−H oxygenations of aromatic hydrocarbons and C3‐substituted indoles were studied by employing a co‐catalytic system of... 
oxygenation | quinones | C−H activation | photocatalysis | hydrocarbons | Quinone | Analysis | Catalysis
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 15, pp. 2186 - 2193
The investigation of photoredox‐induced intra‐ and intermolecular radical [4+2] annulations of indoles confronted us with a puzzling dichotomous behavior of... 
Density functional calculations | Cyclization | Nitrogen heterocycles | Reaction mechanisms | Photocatalysis | CATALYSIS | THERMOCHEMISTRY | VISIBLE-LIGHT PHOTOREDOX | ARYLATION | CHEMISTRY, ORGANIC | POTENTIALS | FUNCTIONALIZATION | HETEROCYCLES | DERIVATIVES | TRIFLUOROMETHYLATION
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 07/2018, Volume 24, Issue 40, pp. 10253 - 10259
Few natural oxindole alkaloids possess an exceptional spiro‐[(1,3)oxazinan‐3,6′‐oxindole] core structure, which results from an unusual oxidative indole... 
reaction mechanisms | photochemistry | spiro compounds | rearrangement | alkaloids | YIELDS | ACID | MECHANISM | OXINDOLE | CHEMISTRY, MULTIDISCIPLINARY | SPIROOXINDOLES | RESERPINE | LASER-FLASH-PHOTOLYSIS | Enantiomers | Reserpine | Corticosteroids | Alkaloids | Anthraquinone | Indole | Oxindole alkaloids | Catalysis | Ring opening | Oxazine
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2015, Volume 21, Issue 35, pp. 12308 - 12312
Journal Article
Chemical Communications: Chem Comm, ISSN 1359-7345, 01/2016, Volume 52, Issue 5, pp. 1025 - 1028
Common photoredox catalysts Ru(bpy) sub(3) super(2+) and Ru(bpz) sub(3) super(2+) are rapidly converted into Ruthenium(viii)-oxide through continuous visible... 
Light irradiation | Catalysts | Cations | Oxidation | Catalysis | Radicals
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 06/2017, Volume 2017, Issue 22, pp. 3134 - 3138
A common synthetic route to indoxyl and 2‐oxindole alkaloids utilizes the oxidation of indoles to 3‐hydroxyindolenines, followed by acid‐mediated... 
Phosphoric acids | Heterocycles | Alkaloids | Organocatalysis | Rearrangement | ASYMMETRIC-SYNTHESIS | BOND-FORMING REACTIONS | CHEMISTRY, ORGANIC | OXIDATIVE REARRANGEMENT | SPIROOXINDOLES | STEREOCENTER | PSEUDOINDOXYLS | STEREOCONTROLLED TOTAL-SYNTHESIS | BRONSTED ACIDS | INDOLE ALKALOIDS | DERIVATIVES | Phosphates | Phosphoric acid
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 06/2017, Volume 2017, Issue 22, pp. 3114 - 3114
The cover picture shows the phosphoric acid catalyzed, highly regioselective 1,2‐rearrangement of readily available 3‐hydroxyindolenines into 2‐oxindoles.... 
Phosphates | Phosphoric acid
Journal Article
ChemCatChem, ISSN 1867-3880, 09/2016, Volume 8, Issue 18, pp. 2881 - 2884
Journal Article
ChemCatChem, ISSN 1867-3880, 09/2016, Volume 8, Issue 18, pp. 3002 - 3002
Journal Article
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