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The First Gold(III) Formate: Evidence for β-Hydride Elimination.
- Published in:
- Angewandte Chemie, 2017, v. 129, n. 42, p. 13042, doi. 10.1002/ange.201705557
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Cyclometallierte Au<sup>III</sup>-Komplexe: Synthese, Reaktivität und physikalisch-chemische Eigenschaften.
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- Angewandte Chemie, 2017, v. 129, n. 8, p. 2024, doi. 10.1002/ange.201607225
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- Article
Gold-Catalyzed Direct Oxidative Arylation with Boron Coupling Partners.
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- Angewandte Chemie, 2017, v. 129, n. 4, p. 1041, doi. 10.1002/ange.201610457
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The First Gold(III) Formate: Evidence for β-Hydride Elimination.
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 42, p. 12862, doi. 10.1002/anie.201705557
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- Article
Cyclometalated Gold(III) Complexes: Synthesis, Reactivity, and Physicochemical Properties.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 8, p. 1994, doi. 10.1002/anie.201607225
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- Article
Gold-Catalyzed Direct Oxidative Arylation with Boron Coupling Partners.
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 4, p. 1021, doi. 10.1002/anie.201610457
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- Article
Luminescent (N^C^C) Gold(III) Complexes: Stabilized Gold(III) Fluorides.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 48, p. 14287, doi. 10.1002/anie.201505533
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- Article
Alkoxyallene‐Based LANCA Three‐Component Synthesis of 1,2‐Diketones, Quinoxalines, and Unique Isoindenone Dimers and a Computational Study of the Isoindenone Dimerization.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 11, p. 1753, doi. 10.1002/ejoc.202000116
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- Article
Modular Synthesis of Heterobenzylic Amines via Carbonyl Azinylative Amination.
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- Angewandte Chemie, 2024, v. 136, n. 42, p. 1, doi. 10.1002/ange.202408287
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- Article
Modular Synthesis of Heterobenzylic Amines via Carbonyl Azinylative Amination.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 42, p. 1, doi. 10.1002/anie.202408287
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- Article
Phosphorescent κ<sup>3</sup>‐(N^C^C)‐Gold(III) Complexes: Synthesis, Photophysics, Computational Studies and Application to Solution‐Processable OLEDs.
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- Chemistry - A European Journal, 2020, v. 26, n. 72, p. 17604, doi. 10.1002/chem.202003571
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- Article