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Antifungal Activity of Naphthoquinoidal Compounds <i>In Vitro</i> against Fluconazole-Resistant Strains of Different <i>Candida</i> Species: A Special Emphasis on Mechanisms of Action on <i>Candida tropicalis</i>.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0093698
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Electrochemical Sulphenylation/Cyclization of Quinones: A Rapid, Green, and Efficient Access to Cytotoxic Compounds.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 38, p. 1, doi. 10.1002/ejoc.202300506
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- Article
Ruthenium(II)‐Catalyzed C−H/N−H Alkyne Annulation of Nonsymmetric Imidazoles: Mechanistic Insights by Computation and Photophysical Properties.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 28, p. 1, doi. 10.1002/ejoc.202200590
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Front Cover: Electrochemical Selenation/Cyclization of Quinones: A Rapid, Green and Efficient Access to Functionalized Trypanocidal and Antitumor Compounds (Eur. J. Org. Chem. 29/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 29, p. 4433, doi. 10.1002/ejoc.202001035
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- Article
Electrochemical Selenation/Cyclization of Quinones: A Rapid, Green and Efficient Access to Functionalized Trypanocidal and Antitumor Compounds.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 29, p. 4474, doi. 10.1002/ejoc.202000216
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Ruthenium(II)‐Catalyzed C–H Alkenylation of Quinones: Diversity‐Oriented Strategy for Trypanocidal Compounds.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 13, p. 2344, doi. 10.1002/ejoc.201900004
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- Article
Identification of Nor-β-Lapachone Derivatives as Potential Antibacterial Compounds against Enterococcus faecalis Clinical Strain.
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- Current Microbiology, 2011, v. 62, n. 2, p. 684, doi. 10.1007/s00284-010-9763-6
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It Takes Two to Tango, Part II: Synthesis of A-Ring Functionalised Quinones Containing Two Redox-Active Centres with Antitumour Activities.
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- Molecules, 2023, v. 28, n. 5, p. 2222, doi. 10.3390/molecules28052222
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- Article
Combination of Aryl Diselenides/Hydrogen Peroxide and Carbon‐Nanotube/Rhodium Nanohybrids for Naphthol Oxidation: An Efficient Route towards Trypanocidal Quinones.
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- Chemistry - A European Journal, 2018, v. 24, n. 57, p. 15130, doi. 10.1002/chem.201803538
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Front Cover: Combination of Aryl Diselenides/Hydrogen Peroxide and Carbon‐Nanotube/Rhodium Nanohybrids for Naphthol Oxidation: An Efficient Route towards Trypanocidal Quinones (Chem. Eur. J. 57/2018).
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- Chemistry - A European Journal, 2018, v. 24, n. 57, p. 15126, doi. 10.1002/chem.201803537
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- Article
Combination of Aryl Diselenides/Hydrogen Peroxide and Carbon‐Nanotube/Rhodium Nanohybrids for Naphthol Oxidation: An Efficient Route towards Trypanocidal Quinones.
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- Chemistry - A European Journal, 2018, v. 24, n. 57, p. 15227, doi. 10.1002/chem.201802773
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- Article
Umgehung von Ammoniak: Von N<sub>2</sub> zu stickstoffhaltigen Heterocyclen ohne N<sub>1</sub>‐Zwischenprodukte oder Übergangsmetalle.
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- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202402777
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The Synthesis and Reactivity of Naphthoquinonynes.
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- Angewandte Chemie, 2024, v. 136, n. 18, p. 1, doi. 10.1002/ange.202400188
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The Use of the Mannich Reaction toward Amino‐Based Anthraquinone Applied in Aqueous Redox Flow Battery.
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- Advanced Energy & Sustainability Research, 2024, v. 5, n. 10, p. 1, doi. 10.1002/aesr.202400118
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Bypassing Ammonia: From N<sub>2</sub> to Nitrogen Heterocycles without N<sub>1</sub> Intermediates or Transition Metals.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 21, p. 1, doi. 10.1002/anie.202402777
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- Article
The Synthesis and Reactivity of Naphthoquinonynes.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 18, p. 1, doi. 10.1002/anie.202400188
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- Article
Front Cover: Redox Center Modification of Lapachones towards the Synthesis of Nitrogen Heterocycles as Selective Fluorescent Mitochondrial Imaging Probes (Eur. J. Org. Chem. 26/2017).
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 26, p. 3738, doi. 10.1002/ejoc.201700901
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Redox Center Modification of Lapachones towards the Synthesis of Nitrogen Heterocycles as Selective Fluorescent Mitochondrial Imaging Probes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 26, p. 3763, doi. 10.1002/ejoc.201700227
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- Article
Synthesis of a Phenazine-Based 1,2,3-Triazole from Naturally Occurring Naphthoquinone Designed as a Probe for Cd<sup>2+</sup> Ions.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 4, p. 703, doi. 10.1002/ejoc.201403011
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2,1,3-Benzothiadiazole and Derivatives: Synthesis, Properties, Reactions, and Applications in Light Technology of Small Molecules.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 2, p. 228, doi. 10.1002/ejoc.201201161
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Rational Design and Synthesis of Large Stokes Shift 2,6-Sulphur-Disubstituted BODIPYs for Cell Imaging.
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- Chemosensors, 2022, v. 10, n. 1, p. 19, doi. 10.3390/chemosensors10010019
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Frontispiece: Decoding Directing Groups and Their Pivotal Role in C−H Activation.
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- Chemistry - A European Journal, 2021, v. 27, n. 49, p. 1, doi. 10.1002/chem.202184961
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Decoding Directing Groups and Their Pivotal Role in C−H Activation.
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- Chemistry - A European Journal, 2021, v. 27, n. 49, p. 12453, doi. 10.1002/chem.202101004
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Transition-Metal-Catalyzed Selective Alkynylation of C-H Bonds.
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- Advanced Synthesis & Catalysis, 2021, v. 363, n. 22, p. 4994, doi. 10.1002/adsc.202100992
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Special issue: The Brazilian Meeting on Organic Synthesis.
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- Chemical Record, 2021, v. 21, n. 10, p. 2602, doi. 10.1002/tcr.202100247
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Imidazoles and Oxazoles from Lapachones and Phenanthrene‐9,10‐dione: A Journey through their Synthesis, Biological Studies, and Optical Applications.
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- Chemical Record, 2021, v. 21, n. 10, p. 2702, doi. 10.1002/tcr.202100138
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The Different Facets of Metal‐Catalyzed C−H Functionalization Involving Quinone Compounds.
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- Chemical Record, 2021, v. 21, n. 10, p. 2604, doi. 10.1002/tcr.202000163
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- Article
Synthesis of Selenium-Quinone Hybrid Compounds with Potential Antitumor Activity via Rh-Catalyzed C-H Bond Activation and Click Reactions.
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- Molecules, 2018, v. 23, n. 1, p. 83, doi. 10.3390/molecules23010083
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Antimony(V) and Bismuth(V) Complexes of Lapachol: Synthesis, Crystal Structure and Cytotoxic Activity.
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- Molecules, 2011, v. 16, n. 12, p. 10314, doi. 10.3390/molecules161210314
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- Article