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Frontispiz: Metallfreie, elektrochemische Synthese von Sulfonamiden direkt aus (Hetero)arenen, SO<sub>2</sub> und Aminen.
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- Angewandte Chemie, 2021, v. 133, n. 10, p. 1, doi. 10.1002/ange.202016164
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Frontispiz: Metallfreie, elektrochemische Synthese von Sulfonamiden direkt aus (Hetero)arenen, SO<sub>2</sub> und Aminen.
- Published in:
- Angewandte Chemie, 2021, v. 133, n. 10, p. 1, doi. 10.1002/ange.202016164
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- Publication type:
- Article
Metallfreie, elektrochemische Synthese von Sulfonamiden direkt aus (Hetero)arenen, SO<sub>2</sub> und Aminen.
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- Angewandte Chemie, 2021, v. 133, n. 10, p. 5114, doi. 10.1002/ange.202016164
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Dehydrierende anodische C‐C‐Kupplung von Phenolen mit elektronenziehenden Substituenten.
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- Angewandte Chemie, 2020, v. 132, n. 1, p. 323, doi. 10.1002/ange.201910077
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Innentitelbild: Regioselektive metall‐ und reagenzfreie Arylierung von Benzothiophenen durch dehydrierende Elektrosynthese (Angew. Chem. 40/2018).
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13162, doi. 10.1002/ange.201810303
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Regioselektive metall‐ und reagenzfreie Arylierung von Benzothiophenen durch dehydrierende Elektrosynthese.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13509, doi. 10.1002/ange.201808555
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- Article
Layered Thiadiazoloquinoxaline‐Containing Long Pyrene‐Fused N‐Heteroacenes.
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- Angewandte Chemie, 2018, v. 130, n. 38, p. 12555, doi. 10.1002/ange.201803230
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Innenrücktitelbild: Metall‐ und reagensfreie dehydrierende formale Benzyl‐Aryl‐Kreuzkupplung durch anodische Aktivierung in 1,1,1,3,3,3‐Hexafluorpropan‐2‐ol (Angew. Chem. 37/2018).
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- Angewandte Chemie, 2018, v. 130, n. 37, p. 12355, doi. 10.1002/ange.201808283
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Metall‐ und reagensfreie dehydrierende formale Benzyl‐Aryl‐Kreuzkupplung durch anodische Aktivierung in 1,1,1,3,3,3‐Hexafluorpropan‐2‐ol.
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- Angewandte Chemie, 2018, v. 130, n. 37, p. 12312, doi. 10.1002/ange.201804997
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Rücktitelbild: Eine regio‐ und diastereoselektive anodische Aryl‐Aryl‐Kupplung in der biomimetischen Totalsynthese von (−)‐Thebain (Angew. Chem. 34/2018).
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- Angewandte Chemie, 2018, v. 130, n. 34, p. 11248, doi. 10.1002/ange.201806821
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Eine regio‐ und diastereoselektive anodische Aryl‐Aryl‐Kupplung in der biomimetischen Totalsynthese von (−)‐Thebain.
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- Angewandte Chemie, 2018, v. 130, n. 34, p. 11221, doi. 10.1002/ange.201803887
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- Article
Einfache und doppelte metall- und reagensfreie anodische C-C-Kreuzkupplung von Phenolen mit Thiophenen.
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- Angewandte Chemie, 2017, v. 129, n. 46, p. 14920, doi. 10.1002/ange.201708946
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Reagens- und metallfreie anodische C-C-Kreuzkupplung von Anilinderivaten.
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- Angewandte Chemie, 2017, v. 129, n. 17, p. 4955, doi. 10.1002/ange.201612613
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- Article
Innentitelbild: Reagens- und metallfreie anodische C-C-Kreuzkupplung von Anilinderivaten (Angew. Chem. 17/2017).
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- Angewandte Chemie, 2017, v. 129, n. 17, p. 4704, doi. 10.1002/ange.201702483
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- Article
Selektive Synthese teilgeschützter unsymmetrischer Biphenole durch reagens- und metallfreie anodische Kreuzkupplung.
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- Angewandte Chemie, 2016, v. 128, n. 39, p. 11979, doi. 10.1002/ange.201604321
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Titelbild: Selektive Synthese teilgeschützter unsymmetrischer Biphenole durch reagens- und metallfreie anodische Kreuzkupplung (Angew. Chem. 39/2016).
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- Angewandte Chemie, 2016, v. 128, n. 39, p. 11863, doi. 10.1002/ange.201606627
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Synthese von meta-Terphenyl-2,2′′-diolen durch anodische C-C-Kreuzkupplungen.
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- Angewandte Chemie, 2016, v. 128, n. 36, p. 11031, doi. 10.1002/ange.201605865
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Zugang zu Pyrazolidin-3,5-dionen durch anodischen N-N-Bindungsaufbau.
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- Angewandte Chemie, 2016, v. 128, n. 32, p. 9587, doi. 10.1002/ange.201603899
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Inside Cover: Regioselective Metal‐ and Reagent‐Free Arylation of Benzothiophenes by Dehydrogenative Electrosynthesis (Angew. Chem. Int. Ed. 40/2018).
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- Angewandte Chemie International Edition, 2018, v. 57, n. 40, p. 12980, doi. 10.1002/anie.201810303
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- Article
Regioselective Metal‐ and Reagent‐Free Arylation of Benzothiophenes by Dehydrogenative Electrosynthesis.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 40, p. 13325, doi. 10.1002/anie.201808555
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- Article
Layered Thiadiazoloquinoxaline‐Containing Long Pyrene‐Fused N‐Heteroacenes.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 38, p. 12375, doi. 10.1002/anie.201803230
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- Article
Inside Back Cover: Metal‐ and Reagent‐Free Dehydrogenative Formal Benzyl–Aryl Cross‐Coupling by Anodic Activation in 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol (Angew. Chem. Int. Ed. 37/2018).
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- Angewandte Chemie International Edition, 2018, v. 57, n. 37, p. 12177, doi. 10.1002/anie.201808283
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- Article
Metal‐ and Reagent‐Free Dehydrogenative Formal Benzyl–Aryl Cross‐Coupling by Anodic Activation in 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 37, p. 12136, doi. 10.1002/anie.201804997
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- Article
Back Cover: A Regio‐ and Diastereoselective Anodic Aryl–Aryl Coupling in the Biomimetic Total Synthesis of (−)‐Thebaine (Angew. Chem. Int. Ed. 34/2018).
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- Angewandte Chemie International Edition, 2018, v. 57, n. 34, p. 11080, doi. 10.1002/anie.201806821
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- Article
A Regio‐ and Diastereoselective Anodic Aryl–Aryl Coupling in the Biomimetic Total Synthesis of (−)‐Thebaine.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 34, p. 11055, doi. 10.1002/anie.201803887
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Single and Twofold Metal- and Reagent-Free Anodic C−C Cross-Coupling of Phenols with Thiophenes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 46, p. 14727, doi. 10.1002/anie.201708946
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Reagent- and Metal-Free Anodic C−C Cross-Coupling of Aniline Derivatives.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 17, p. 4877, doi. 10.1002/anie.201612613
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- Article
Inside Cover: Reagent- and Metal-Free Anodic C−C Cross-Coupling of Aniline Derivatives (Angew. Chem. Int. Ed. 17/2017).
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- Angewandte Chemie International Edition, 2017, v. 56, n. 17, p. 4632, doi. 10.1002/anie.201702483
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Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent- and Metal-Free Anodic Cross-Coupling Reaction.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 39, p. 11801, doi. 10.1002/anie.201604321
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Cover Picture: Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent- and Metal-Free Anodic Cross-Coupling Reaction (Angew. Chem. Int. Ed. 39/2016).
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- Angewandte Chemie International Edition, 2016, v. 55, n. 39, p. 11689, doi. 10.1002/anie.201606627
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Synthesis of meta-Terphenyl-2,2′′-diols by Anodic C−C Cross-Coupling Reactions.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 36, p. 10872, doi. 10.1002/anie.201605865
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Access to Pyrazolidin-3,5-diones through Anodic N-N Bond Formation.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 32, p. 9437, doi. 10.1002/anie.201603899
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Hexasubstituted Benzenes with Ultrastrong Dipole Moments.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 9, p. 3220, doi. 10.1002/anie.201508249
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Metal‐ and Reagent‐Free Highly Selective Anodic Cross‐Coupling Reaction of Phenols.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 20, p. 5210, doi. 10.1002/anie.201401136
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Cover Picture: Metal- and Reagent-Free Highly Selective Anodic Cross-Coupling Reaction of Phenols (Angew. Chem. Int. Ed. 20/2014).
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- Angewandte Chemie International Edition, 2014, v. 53, n. 20, p. 4979, doi. 10.1002/anie.201401136
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- Publication type:
- Article
Metal- and Reagent-Free Highly Selective Anodic Cross-Coupling Reaction of Phenols.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 20, p. 5210, doi. 10.1002/anie.201401136
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- Article
Powerful Fluoroalkoxy Molybdenum(V) Reagent for Selective Oxidative Arene Coupling Reaction.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 9, p. 2494, doi. 10.1002/anie.201309287
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- Article
Cycloaddition reactions of 2 H-1-benzothietes and 1,3,5,7-tetrathio- s-indacene-2,6-dithiones.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2016, v. 71, n. 8, p. 891, doi. 10.1515/znb-2016-0063
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Crystal structure of a dimeric 1-benzothiepin.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2016, v. 71, n. 4, p. 345, doi. 10.1515/znb-2015-0201
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Dimeric Capsules Formed by Tetra-CMPO Derivatives of (Thia)Calix[4]arenes.
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- Chemistry - An Asian Journal, 2010, v. 5, n. 6, p. 1347, doi. 10.1002/asia.200900607
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2-(2,5-Dimethoxyphenyl)pyrrole-3-carbonitrile.
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- Molbank, 2023, v. 2023, n. 2, p. M1627, doi. 10.3390/M1627
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(S)-3-(3-((7-Ethynyl-9 H -pyrimido[4,5- b ]indol-4-yl)amino)piperidin-1-yl)propanenitrile.
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- Molbank, 2022, v. 2022, n. 3, p. M1437, doi. 10.3390/M1437
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2,5-Bis((E)-2-ferrocenylvinyl)- N , N , N′ , N′ -tetrapropylbenzene-1,4-diamine.
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- Molbank, 2022, v. 2022, n. 3, p. M1420, doi. 10.3390/M1420
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12 H -Dibenzo[ d , g ][1,2,3]triselenocin-12-ol.
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- Molbank, 2022, v. 2022, n. 3, p. M1418, doi. 10.3390/M1418
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6-(2′-(4″-Oxabutyloxy)phenyl)-1,6,11-triaza-3,9,14,17,22,25-hexaoxa-2(1,2)(4-methylbenzena)-10(1,2)(5-methylbenzena)bicyclo(9.8.8)heptacosaphane Sodium Bromide Dichloromethane.
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- Molbank, 2022, v. 2022, n. 1, p. M1348, doi. 10.3390/M1348
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N -(6-Chloro-3-nitropyridin-2-yl)-5-(1-methyl-1 H -pyrazol-4-yl)isoquinolin-3-amine.
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- Molbank, 2021, v. 2021, n. 1, p. M1181, doi. 10.3390/M1181
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N1-{4-[2-(Methylthio)-1H-imidazol-5-yl]pyridin-2-yl}benzene-1,4-diamine.
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- Molbank, 2019, v. 2019, n. 1, p. M1048, doi. 10.3390/M1048
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Stereoselective Synthesis of Polycyclic Thiopyrans.
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- Journal of Heterocyclic Chemistry, 2012, v. 49, n. 3, p. 516, doi. 10.1002/jhet.789
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Preparation of 5-bromo-6-phenylimidazo[2,1- b][1,3,4]thiadiazol-2-ylamines.
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- Journal of Heterocyclic Chemistry, 2008, v. 45, n. 1, p. 299, doi. 10.1002/jhet.5570450138
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Synthesis of pyrrolo[3′,4′:2,3]azepino[4,5,6- cd]indole-8,10-diones.
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- Journal of Heterocyclic Chemistry, 2000, v. 37, n. 5, p. 1177, doi. 10.1002/jhet.5570370526
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- Article