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The Bis(η<sup>6</sup>‐benzene)lithium Cation: A Fundamental Main‐Group Organometallic Species.
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- Angewandte Chemie, 2021, v. 133, n. 42, p. 23061, doi. 10.1002/ange.202108376
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Mechanismus der Aren‐limitierten, nicht‐dirigierten C‐H‐Aktivierung von Arenen mit Palladium.
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- Angewandte Chemie, 2021, v. 133, n. 28, p. 15770, doi. 10.1002/ange.202105092
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Synthese von trifluorierten Tetralinen durch I(I)/I(III)‐katalysierte Ringexpansion: programmieren von Konformationen über [CH<sub>2</sub>CH<sub>2</sub>] → [CF<sub>2</sub>CHF] Isosterismus.
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- Angewandte Chemie, 2021, v. 133, n. 24, p. 13760, doi. 10.1002/ange.202102222
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Desymmetrisierung von prochiralen Cyclobutanonen via Stickstoffinsertion: Ein einfacher Zugang zu chiralen γ‐Lactamen.
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- Angewandte Chemie, 2021, v. 133, n. 17, p. 9805, doi. 10.1002/ange.202100642
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The [(NHC)B(H)C<sub>6</sub>F<sub>5</sub>]<sup>+</sup> Cations and Their [B](H)−CO Borane Carbonyls.
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- Angewandte Chemie, 2020, v. 132, n. 48, p. 21644, doi. 10.1002/ange.202009353
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Using the Secondary PH/BH Functional Groups of an Active Geminal Frustrated Lewis Pair for Carbon Monoxide Reduction and Reactions with Nitriles and Isonitriles.
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- Angewandte Chemie, 2020, v. 132, n. 30, p. 12577, doi. 10.1002/ange.202000612
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Stabile Silanoltriaden im Zeolithkatalysator SSZ‐70.
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- Angewandte Chemie, 2020, v. 132, n. 27, p. 11032, doi. 10.1002/ange.202001364
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Geometric E→Z Isomerisation of Alkenyl Silanes by Selective Energy Transfer Catalysis: Stereodivergent Synthesis of Triarylethylenes via a Formal anti‐Metallometallation.
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- Angewandte Chemie, 2019, v. 131, n. 51, p. 18792, doi. 10.1002/ange.201910169
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Multi‐Component Synthesis of Rare 1,3‐Dihydro‐1,3‐azaborinine Derivatives: Application of a Bora‐Nazarov Type Reaction.
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- Angewandte Chemie, 2019, v. 131, n. 43, p. 15521, doi. 10.1002/ange.201909530
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Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism.
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- Angewandte Chemie, 2019, v. 131, n. 32, p. 11106, doi. 10.1002/ange.201905452
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Palladiumkatalysierte decarboxylierende γ‐Arylierung: Ein Zugang zu tetrasubstituierten chiralen Allenen.
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- Angewandte Chemie, 2019, v. 131, n. 20, p. 6616, doi. 10.1002/ange.201901848
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Synthese einer NHC‐koordinierten Siliciumringverbindung mit Si=N‐Gruppe und einem zweifachkoordinierten Siliciumatom.
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- Angewandte Chemie, 2019, v. 131, n. 13, p. 4440, doi. 10.1002/ange.201813674
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Titelbild: Bioinspirierte radikalische Stetter‐Reaktion: radikalische Umpolung, ermöglicht durch Ionenpaar‐Photokatalyse (Angew. Chem. 4/2019).
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 931, doi. 10.1002/ange.201813835
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- Article
Bioinspirierte radikalische Stetter‐Reaktion: radikalische Umpolung, ermöglicht durch Ionenpaar‐Photokatalyse.
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 1221, doi. 10.1002/ange.201813835
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Selbstanordnung von BODIPY‐Farbstoffen als Werkzeug, um die Antitumoraktivität von Capsaicin bei Prostatakrebs zu erhöhen.
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- Angewandte Chemie, 2018, v. 130, n. 52, p. 17481, doi. 10.1002/ange.201804783
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Innenrücktitelbild: Metal‐Free Radical Borylation of Alkyl and Aryl Iodides (Angew. Chem. 51/2018).
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- Angewandte Chemie, 2018, v. 130, n. 51, p. 17151, doi. 10.1002/ange.201813329
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Metal‐Free Radical Borylation of Alkyl and Aryl Iodides.
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- Angewandte Chemie, 2018, v. 130, n. 51, p. 17074, doi. 10.1002/ange.201810782
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Nucleophilic Activation of Sulfur Hexafluoride: Metal‐Free, Selective Degradation by Phosphines.
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- Angewandte Chemie, 2018, v. 130, n. 18, p. 5045, doi. 10.1002/ange.201713206
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Diradikaloid oder zwitterionischer Charakter: die ungesättigte Verbindung [Si<sub>4</sub>{N(SiMe<sub>3</sub>)Dipp}<sub>4</sub>] mit gefaltetem Si<sub>4</sub>-Strukturmotiv.
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- Angewandte Chemie, 2017, v. 129, n. 44, p. 14054, doi. 10.1002/ange.201705787
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Radikalische Hydrodehalogenierung von Arylbromiden und -chloriden mit Natriumhydrid und 1,4-Dioxan.
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- Angewandte Chemie, 2017, v. 129, n. 43, p. 13459, doi. 10.1002/ange.201706534
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Einfache Modulierung von FLP-Eigenschaften: ein Phosphanylvinyl-Grignard-Reagenz und Ga/P- oder In/P<sub>2</sub>-basierte frustrierte Lewis-Paare.
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- Angewandte Chemie, 2017, v. 129, n. 11, p. 3140, doi. 10.1002/ange.201612485
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Schwefelylide durch (3+2)-Cycloaddition von Arinen mit Vinylsulfiden - stereoselektive Synthese hoch substituierter Alkene.
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- Angewandte Chemie, 2016, v. 128, n. 46, p. 14649, doi. 10.1002/ange.201608144
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Oberflächen-Dominoreaktion: Glaser-Kupplung und dehydrierende Kupplung von Dicarbonsäuren unter Bildung eines polymeren Bisacylperoxids.
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- Angewandte Chemie, 2016, v. 128, n. 33, p. 9929, doi. 10.1002/ange.201602859
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Radical Hydrodeiodination of Aryl, Alkenyl, Alkynyl, and Alkyl Iodides with an Alcoholate as Organic Chain Reductant through Electron Catalysis.
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- Angewandte Chemie, 2016, v. 128, n. 23, p. 6861, doi. 10.1002/ange.201601930
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Formation of Thermally Robust Frustrated Lewis Pairs by Electrocyclic Ring Closure Reactions.
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- Angewandte Chemie, 2016, v. 128, n. 18, p. 5616, doi. 10.1002/ange.201510994
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- Article
Cover Picture: Bioinspired Radical Stetter Reaction: Radical Umpolung Enabled by Ion‐Pair Photocatalysis (Angew. Chem. Int. Ed. 4/2019).
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- Angewandte Chemie International Edition, 2019, v. 58, n. 4, p. 919, doi. 10.1002/anie.201813835
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Bioinspired Radical Stetter Reaction: Radical Umpolung Enabled by Ion‐Pair Photocatalysis.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 4, p. 1208, doi. 10.1002/anie.201809601
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Hierarchical Self‐Assembly of BODIPY Dyes as a Tool to Improve the Antitumor Activity of Capsaicin in Prostate Cancer.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 52, p. 17235, doi. 10.1002/anie.201804783
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Inside Back Cover: Metal‐Free Radical Borylation of Alkyl and Aryl Iodides (Angew. Chem. Int. Ed. 51/2018).
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- Angewandte Chemie International Edition, 2018, v. 57, n. 51, p. 16907, doi. 10.1002/anie.201813329
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- Article
Metal‐Free Radical Borylation of Alkyl and Aryl Iodides.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 51, p. 16832, doi. 10.1002/anie.201810782
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- Publication type:
- Article
Nucleophilic Activation of Sulfur Hexafluoride: Metal-Free, Selective Degradation by Phosphines.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 18, p. 4951, doi. 10.1002/anie.201713206
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- Article
Diradicaloid or Zwitterionic Character: The Non-Tetrahedral Unsaturated Compound [Si<sub>4</sub>{N(SiMe<sub>3</sub>)Dipp}<sub>4</sub>] with a Butterfly-type Si<sub>4</sub> Substructure.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 44, p. 13866, doi. 10.1002/anie.201705787
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Radical Hydrodehalogenation of Aryl Bromides and Chlorides with Sodium Hydride and 1,4-Dioxane.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 43, p. 13275, doi. 10.1002/anie.201706534
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- Article
Facile Modulation of FLP Properties: A Phosphinylvinyl Grignard Reagent and Ga/P- and In/P<sub>2</sub>-Based Frustrated Lewis Pairs.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 11, p. 3094, doi. 10.1002/anie.201612485
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- Article
Sulfonium Ylides by (3+2) Cycloaddition of Arynes with Vinyl Sulfides: Stereoselective Synthesis of Highly Substituted Alkenes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 46, p. 14435, doi. 10.1002/anie.201608144
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On-Surface Domino Reactions: Glaser Coupling and Dehydrogenative Coupling of a Biscarboxylic Acid To Form Polymeric Bisacylperoxides.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 33, p. 9777, doi. 10.1002/anie.201602859
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- Article
Radical Hydrodeiodination of Aryl, Alkenyl, Alkynyl, and Alkyl Iodides with an Alcoholate as Organic Chain Reductant through Electron Catalysis.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 23, p. 6749, doi. 10.1002/anie.201601930
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- Article
Formation of Thermally Robust Frustrated Lewis Pairs by Electrocyclic Ring Closure Reactions.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 18, p. 5526, doi. 10.1002/anie.201510994
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- Article
Ortho-Trialkylstannyl Arylphosphanes by C-P and C-Sn Bond Formation in Arynes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 2, p. 802, doi. 10.1002/anie.201509329
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Observation of a Thermally Induced Bora-Nazarov Cyclization at a Phosphole Framework.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 42, p. 12366, doi. 10.1002/anie.201502850
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6-Trifluoromethyl-Phenanthridines through Radical Trifluoromethylation of Isonitriles.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 41, p. 10792, doi. 10.1002/anie.201306082
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Noncovalent Interactions in Organocatalysis: Modulating Conformational Diversity and Reactivity in the MacMillan Catalyst.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 31, p. 7967, doi. 10.1002/anie.201301864
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Radical-Transfer Hydroamination of Olefins with N-Aminated Dihydropyridines.
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- Chemistry - An Asian Journal, 2011, v. 6, n. 5, p. 1197, doi. 10.1002/asia.201000881
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Evidence for a Rapid Degenerate Hetero-Cope-Type Rearrangement in [Cp*W(S)<sub>2</sub>S-CH<sub>2</sub>-CHCH<sub>2</sub>].
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- Chemistry - An Asian Journal, 2009, v. 4, n. 12, p. 1830, doi. 10.1002/asia.200900360
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Structural Isomers of C<sub>20</sub> Revisited: The Cage and Bowl Are Almost Isoenergetic.
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- ChemPhysChem, 2002, v. 3, n. 2, p. 207, doi. 10.1002/1439-7641(20020215)3:2<207::AID-CPHC207>3.0.CO;2-#
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Ortho-Trialkylstannylarylphosphane über C-P- und C-Sn-Bindungskn üpfung in Arinen.
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- Angewandte Chemie, 2016, v. 128, n. 2, p. 813, doi. 10.1002/ange.201509329
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Observation of a Thermally Induced Bora-Nazarov Cyclization at a Phosphole Framework.
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- Angewandte Chemie, 2015, v. 127, n. 42, p. 12543, doi. 10.1002/ange.201502850
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- Article
6-Trifluoromethyl-Phenanthridines through Radical Trifluoromethylation of Isonitriles.
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- Angewandte Chemie, 2013, v. 125, n. 41, p. 10992, doi. 10.1002/ange.201306082
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Nichtbindende Wechselwirkungen in der Organokatalyse: Modulierung konformativer Diversität und Reaktivität im MacMillan-Katalysator.
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- Angewandte Chemie, 2013, v. 125, n. 31, p. 8125, doi. 10.1002/ange.201301864
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Hydrogen Activation by an Intramolecular Boron Lewis Acid/Zirconocene Pair.
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- Angewandte Chemie, 2012, v. 124, n. 35, p. 8960, doi. 10.1002/ange.201202218
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