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Electroreductive Cross‐Electrophile Coupling (eXEC) Reactions.
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- Angewandte Chemie, 2023, v. 135, n. 45, p. 1, doi. 10.1002/ange.202306679
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Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes.
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- Angewandte Chemie, 2023, v. 135, n. 45, p. 1, doi. 10.1002/ange.202312803
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- Article
Electroreductive Cross‐Electrophile Coupling (eXEC) Reactions.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 45, p. 1, doi. 10.1002/anie.202306679
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- Article
Organo‐Mediator Enabled Electrochemical Deuteration of Styrenes.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 45, p. 1, doi. 10.1002/anie.202312803
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- Article
Electrochemical NiH‐Catalyzed C(sp<sup>3</sup>)−C(sp<sup>3</sup>) Coupling of Alkyl Halides and Alkyl Alkenes.
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- Angewandte Chemie, 2023, v. 135, n. 44, p. 1, doi. 10.1002/ange.202311941
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- Article
Electrochemical NiH‐Catalyzed C(sp<sup>3</sup>)−C(sp<sup>3</sup>) Coupling of Alkyl Halides and Alkyl Alkenes.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 44, p. 1, doi. 10.1002/anie.202311941
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Electroreductive Cross‐Electrophile Coupling of Aziridines and Aryl Bromides.
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202300959
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- Article
Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO<sub>2</sub>.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202214710
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- Article
Innentitelbild: Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO<sub>2</sub> (Angew. Chem. 3/2023).
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202214710
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- Article
Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO<sub>2</sub>.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 3, p. 1, doi. 10.1002/anie.202214710
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- Article
Inside Cover: Site‐Selective Electrochemical C−H Carboxylation of Arenes with CO<sub>2</sub> (Angew. Chem. Int. Ed. 3/2023).
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- Angewandte Chemie International Edition, 2023, v. 62, n. 3, p. 1, doi. 10.1002/anie.202214710
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- Article
Metal‐Free Electrochemical Carboxylation of Organic Halides in the Presence of Catalytic Amounts of an Organomediator.
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- Angewandte Chemie, 2022, v. 134, n. 41, p. 1, doi. 10.1002/ange.202210201
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- Article
Metal‐Free Electrochemical Carboxylation of Organic Halides in the Presence of Catalytic Amounts of an Organomediator.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 41, p. 1, doi. 10.1002/anie.202210201
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- Article
Electrocarboxylation of Aryl Epoxides with CO<sub>2</sub> for the Facile and Selective Synthesis of β‐Hydroxy Acids.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202207746
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- Article
Electrocarboxylation of Aryl Epoxides with CO<sub>2</sub> for the Facile and Selective Synthesis of β‐Hydroxy Acids.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 38, p. 1, doi. 10.1002/anie.202207746
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Recent Advances in Electrocarboxylation with CO<sub>2</sub>.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 17, p. 1, doi. 10.1002/asia.202200543
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- Article
Facile and general electrochemical deuteration of unactivated alkyl halides.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31435-9
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- Article
Electrochemical Desaturative β‐Acylation of Cyclic N‐Aryl Amines.
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- Angewandte Chemie, 2022, v. 134, n. 6, p. 1, doi. 10.1002/ange.202115178
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- Article
Frontispiz: Electrochemical Desaturative β‐Acylation of Cyclic N‐Aryl Amines.
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- Angewandte Chemie, 2022, v. 134, n. 6, p. 1, doi. 10.1002/ange.202115178
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- Article
Frontispiz: Electrochemical Desaturative β‐Acylation of Cyclic N‐Aryl Amines.
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- Angewandte Chemie, 2022, v. 134, n. 6, p. 1, doi. 10.1002/ange.202280661
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- Article
Electrochemical Desaturative β‐Acylation of Cyclic N‐Aryl Amines.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 6, p. 1, doi. 10.1002/anie.202115178
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- Article
Frontispiece: Electrochemical Desaturative β‐Acylation of Cyclic N‐Aryl Amines.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 6, p. 1, doi. 10.1002/anie.202280661
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- Article
Frontispiece: Electrochemical Desaturative β‐Acylation of Cyclic N‐Aryl Amines.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 6, p. 1, doi. 10.1002/anie.202115178
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- Article
Electrophotocatalytic Undirected C−H Trifluoromethylations of (Het)Arenes.
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- Chemistry - A European Journal, 2020, v. 26, n. 15, p. 3241, doi. 10.1002/chem.201905774
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- Article
Diastereoselective Cyclobutenol Synthesis: A Heterogeneous Palladium‐Catalyzed Oxidative Carbocyclization‐Borylation of Enallenols.
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- Chemistry - A European Journal, 2019, v. 25, n. 1, p. 210, doi. 10.1002/chem.201805118
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- Article
Iridium‐Catalyzed Electrooxidative C−H Activation by Chemoselective Redox‐Catalyst Cooperation.
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- Angewandte Chemie, 2018, v. 130, n. 43, p. 14375, doi. 10.1002/ange.201809611
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- Article
Iridium‐Catalyzed Electrooxidative C−H Activation by Chemoselective Redox‐Catalyst Cooperation.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 43, p. 14179, doi. 10.1002/anie.201809611
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- Article
Catalyst‐ and Reagent‐Free Electrochemical Azole C−H Amination.
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- Chemistry - A European Journal, 2018, v. 24, n. 49, p. 12784, doi. 10.1002/chem.201802832
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- Article
Electrooxidative Ruthenium‐Catalyzed C−H/O−H Annulation by Weak <italic>O</italic>‐Coordination.
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- Angewandte Chemie, 2018, v. 130, n. 20, p. 5920, doi. 10.1002/ange.201802748
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- Article
Electrooxidative Rhodium‐Catalyzed C−H/C−H Activation: Electricity as Oxidant for Cross‐Dehydrogenative Alkenylation.
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- Angewandte Chemie, 2018, v. 130, n. 20, p. 5930, doi. 10.1002/ange.201803342
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- Article
Electrooxidative Ruthenium‐Catalyzed C−H/O−H Annulation by Weak <italic>O</italic>‐Coordination.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 20, p. 5818, doi. 10.1002/anie.201802748
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- Article
Electrooxidative Rhodium‐Catalyzed C−H/C−H Activation: Electricity as Oxidant for Cross‐Dehydrogenative Alkenylation.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 20, p. 5828, doi. 10.1002/anie.201803342
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- Article
Mechanistic Insight into Enantioselective Palladium‐Catalyzed Oxidative Carbocyclization–Borylation of Enallenes.
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- Chemistry - A European Journal, 2018, v. 24, n. 10, p. 2433, doi. 10.1002/chem.201705239
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Selective Palladium-Catalyzed Allenic C−H Bond Oxidation for the Synthesis of [3]Dendralenes.
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- Angewandte Chemie, 2017, v. 129, n. 42, p. 13292, doi. 10.1002/ange.201706211
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Selective Palladium-Catalyzed Allenic C−H Bond Oxidation for the Synthesis of [3]Dendralenes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 42, p. 13112, doi. 10.1002/anie.201706211
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- Article
Highly Selective Olefin-Assisted Pd<sup>II</sup>-Catalyzed Oxidative Alkynylation of Enallenes.
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- Chemistry - A European Journal, 2017, v. 23, n. 33, p. 7896, doi. 10.1002/chem.201701654
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- Article
Enantioselective Palladium-Catalyzed Carbonylative Carbocyclization of Enallenes via Cross-Dehydrogenative Coupling with Terminal Alkynes: Efficient Construction of α-Chirality of Ketones.
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- Angewandte Chemie, 2017, v. 129, n. 16, p. 4606, doi. 10.1002/ange.201612385
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- Article
Enantioselective Palladium-Catalyzed Carbonylative Carbocyclization of Enallenes via Cross-Dehydrogenative Coupling with Terminal Alkynes: Efficient Construction of α-Chirality of Ketones.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 16, p. 4535, doi. 10.1002/anie.201612385
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- Article
Palladium-Catalyzed Oxidative Cascade Carbonylative Spirolactonization of Enallenols.
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- Angewandte Chemie, 2017, v. 129, n. 12, p. 3269, doi. 10.1002/ange.201612384
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- Article
Palladium-Catalyzed Oxidative Cascade Carbonylative Spirolactonization of Enallenols.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 12, p. 3221, doi. 10.1002/anie.201612384
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- Article
Highly Selective Construction of Seven-Membered Carbocycles by Olefin-Assisted Palladium-Catalyzed Oxidative Carbocyclization-Alkoxycarbonylation of Bisallenes.
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- Angewandte Chemie, 2016, v. 128, n. 46, p. 14617, doi. 10.1002/ange.201608247
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- Article
Highly Selective Construction of Seven-Membered Carbocycles by Olefin-Assisted Palladium-Catalyzed Oxidative Carbocyclization-Alkoxycarbonylation of Bisallenes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 46, p. 14405, doi. 10.1002/anie.201608247
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- Article
Berichtigung: Enzyme- and Ruthenium-Catalyzed Enantioselective Transformation of α-Allenic Alcohols into 2,3-Dihydrofurans.
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- Angewandte Chemie, 2016, v. 128, n. 24, p. 6923, doi. 10.1002/ange.201603735
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Corrigendum: Enzyme- and Ruthenium-Catalyzed Enantioselective Transformation of α-Allenic Alcohols into 2,3-Dihydrofurans.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 24, p. 6812, doi. 10.1002/anie.201603735
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- Article
Palladium-Catalyzed Oxidative Carbocyclization-Borylation of Enallenes to Cyclobutenes.
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- Angewandte Chemie, 2016, v. 128, n. 22, p. 6630, doi. 10.1002/ange.201601613
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- Article
Palladium-Catalyzed Oxidative Carbocyclization-Borylation of Enallenes to Cyclobutenes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 22, p. 6520, doi. 10.1002/anie.201601613
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- Article
Enzyme- and Ruthenium-Catalyzed Enantioselective Transformation of α-Allenic Alcohols into 2,3-Dihydrofurans.
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- Angewandte Chemie, 2016, v. 128, n. 18, p. 5658, doi. 10.1002/ange.201601505
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- Article
Enzyme- and Ruthenium-Catalyzed Enantioselective Transformation of α-Allenic Alcohols into 2,3-Dihydrofurans.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 18, p. 5568, doi. 10.1002/anie.201601505
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- Article
Olefin-Directed Palladium-Catalyzed Regio- and Stereoselective Hydroboration of Allenes.
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- Chemistry - A European Journal, 2016, v. 22, n. 9, p. 2939, doi. 10.1002/chem.201505130
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- Article
Asymmetric Construction of Six-Membered Rings by Cyclization of Allenes with Dinuclear Gold Catalysis.
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- Chemistry - A European Journal, 2015, v. 21, n. 45, p. 15939, doi. 10.1002/chem.201503179
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- Article