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Porphyrin Atropisomerism as a Molecular Engineering Tool in Medicinal Chemistry, Molecular Recognition, Supramolecular Assembly, and Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202401559
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Supramolecular Chirogenesis in a Sterically Hindered Porphyrin: A Critical Theoretical Analysis.
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- Chemistry - A European Journal, 2023, v. 29, n. 49, p. 1, doi. 10.1002/chem.202302275
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Front Cover: Supramolecular Chirogenesis in a Sterically Hindered Porphyrin: A Critical Theoretical Analysis (Chem. Eur. J. 49/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 49, p. 1, doi. 10.1002/chem.202302274
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Supramolecular Chirogenesis in a Sterically Hindered Porphyrin: A Critical Theoretical Analysis**.
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- Chemistry - A European Journal, 2023, v. 29, n. 49, p. 1, doi. 10.1002/chem.202301408
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Influence of meso-linker attachment on the formation of core···π interactions in urea-functionalized porphyrins.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2020, v. 75, n. 8, p. 755, doi. 10.1515/znb-2020-0099
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Sustainable water treatment in aquaculture - photolysis and photodynamic therapy for the inactivation of Vibrio species.
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- Aquaculture Research, 2017, v. 48, n. 6, p. 2954, doi. 10.1111/are.13128
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- Article
Comparative Synthetic Strategies for the Generation of 5,10- and 5,15-Substituted Push-Pull Porphyrins.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 25, p. 3565, doi. 10.1002/ejoc.201700093
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Sequential Nucleophilic Substitution of the α-Pyrrole and p-Aryl Positions of meso-Pentafluorophenyl-Substituted BODIPYs.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 22, p. 3187, doi. 10.1002/ejoc.201700264
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Preparation of Tri- and Hexasubstituted Triptycene Synthons by Transition Metal Catalyzed Cross-Coupling Reactions for Post-Modifications.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 1, p. 185, doi. 10.1002/ejoc.201501272
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Simple Porphyrin Desymmetrization: 5,10,15,20-Tetrakis(3-hydroxyphenyl)porphyrin ( mTHPP) as a Gateway Molecule for Peripheral Functionalization.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 20, p. 4283, doi. 10.1002/ejoc.201402433
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Synthesis and Functionalization of Triply Fused Porphyrin Dimers.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 18, p. 3700, doi. 10.1002/ejoc.201201622
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- Article
Synthesis and Reactivity of Allenylporphyrins.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 8, p. 1566, doi. 10.1002/ejoc.201201535
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Porphyrin Dimers and Arrays.
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- European Journal of Organic Chemistry, 2011, v. 2011, n. 29, p. 5817, doi. 10.1002/ejoc.201100642
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- Article
5,15-A<sub>2</sub>B<sub>2</sub>- and 5,15-A<sub>2</sub>BC-Type Porphyrins with Donor and Acceptor Groups for Use in Nonlinear Optics and Photodynamic Therapy (Eur. J. Org. Chem. 29/2011).
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- European Journal of Organic Chemistry, 2011, v. 2011, n. 29, p. n/a, doi. 10.1002/ejoc.201100641
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- Article
5,15-A<sub>2</sub>B<sub>2</sub>- and 5,15-A<sub>2</sub>BC-Type Porphyrins with Donor and Acceptor Groups for Use in Nonlinear Optics and Photodynamic Therapy.
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- European Journal of Organic Chemistry, 2011, v. 2011, n. 29, p. 5797, doi. 10.1002/ejoc.201100641
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Inside Cover: Conformational Re‐engineering of Porphyrins as Receptors with Switchable N−H⋅⋅⋅X‐Type Binding Modes (Angew. Chem. Int. Ed. 46/2019).
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- Angewandte Chemie International Edition, 2019, v. 58, n. 46, p. 16332, doi. 10.1002/anie.201912941
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- Article
Conformational Re‐engineering of Porphyrins as Receptors with Switchable N−H⋅⋅⋅X‐Type Binding Modes.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 46, p. 16553, doi. 10.1002/anie.201907929
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Molecular Engineering of Free‐Base Porphyrins as Ligands—The N−H⋅⋅⋅X Binding Motif in Tetrapyrroles.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 2, p. 418, doi. 10.1002/anie.201806281
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Synthesis and Biological Evaluation of a Library of Glycoporphyrin Compounds.
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- Chemistry - A European Journal, 2012, v. 18, n. 46, p. 14671, doi. 10.1002/chem.201202064
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5,10-A<sub>2</sub>B<sub>2</sub>-Type meso-Substituted Porphyrins-A Unique Class of Porphyrins with a Realigned Dipole Moment.
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- Chemistry - A European Journal, 2011, v. 17, n. 48, p. 13562, doi. 10.1002/chem.201101934
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Bridging the Gap between Porphyrins and Porphycenes: Substituent-Position-Sensitive Tautomerism and Photophysics in meso-Diphenyloctaethylporphyrins.
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- Chemistry - A European Journal, 2011, v. 17, n. 36, p. 10039, doi. 10.1002/chem.201100902
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Molecular Symmetry and Art: Visualizing the Near‐Symmetry of Molecules in Piet Mondrian's De Stijl.
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- Angewandte Chemie, 2024, v. 136, n. 25, p. 1, doi. 10.1002/ange.202403754
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A Heterometallic Porphyrin Dimer as a Potential Quantum Gate: Magneto‐Structural Correlations and Spin Coherence Properties.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202312936
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Bicyclo[1.1.1]pentane Embedded in Porphyrinoids**.
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- Angewandte Chemie, 2023, v. 135, n. 26, p. 1, doi. 10.1002/ange.202302771
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On‐Surface Synthesis of Polyphenylene Wires Comprising Rigid Aliphatic Bicyclo[1.1.1]Pentane Isolator Units.
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- Angewandte Chemie, 2023, v. 135, n. 19, p. 1, doi. 10.1002/ange.202218211
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Innentitelbild: Konformativer Umbau von Porphyrinen als Rezeptoren mit schaltbaren N‐H⋅⋅⋅X‐Bindungsmodi (Angew. Chem. 46/2019).
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- Angewandte Chemie, 2019, v. 131, n. 46, p. 16482, doi. 10.1002/ange.201912941
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- Article
Konformativer Umbau von Porphyrinen als Rezeptoren mit schaltbaren N‐H⋅⋅⋅X‐Bindungsmodi.
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- Angewandte Chemie, 2019, v. 131, n. 46, p. 16705, doi. 10.1002/ange.201907929
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The human tRNA-guanine transglycosylase displays promiscuous nucleobase preference but strict tRNA specificity.
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- Nucleic Acids Research, 2021, v. 49, n. 9, p. 4877, doi. 10.1093/nar/gkab289
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Extroverted Confusion-Linus Pauling, Melvin Calvin, and Porphyrin Isomers.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 19, p. 4272, doi. 10.1002/anie.201003660
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Book Review: Antimalarial Chemotherapy Mechanisms of Action, Resistance, and New Directions in Drug Discovery Edited by Philip J. Rosenthal.
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- ChemBioChem, 2002, v. 3, n. 2/3, p. 261, doi. 10.1002/1439-7633(20020301)3:2/3<261::AID-CBIC261>3.0.CO;2-B
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The Malaria Pigment Haemozoin-A Focal Point of Action for Antimalarial Drugs.
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- ChemBioChem, 2000, v. 1, n. 4, p. 247, doi. 10.1002/1439-7633(20001117)1:4<247::AID-CBIC247>3.0.CO;2-O
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Self-Organization of Porphyrin–POM Dyads: Nonplanar Diacids and Oxoanions in Low-Dimensional H-Bonding Networks.
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- Molecules, 2022, v. 27, n. 20, p. 7060, doi. 10.3390/molecules27207060
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Metal Coordination Effects on the Photophysics of Dipyrrinato Photosensitizers.
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- Molecules, 2022, v. 27, n. 20, p. 6967, doi. 10.3390/molecules27206967
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Development of Antimicrobial Laser-Induced Photodynamic Therapy Based on Ethylcellulose/Chitosan Nanocomposite with 5,10,15,20-Tetrakis(m -Hydroxyphenyl)porphyrin.
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- Molecules, 2021, v. 26, n. 12, p. 3551, doi. 10.3390/molecules26123551
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2D Porphyrinic Metal-Organic Frameworks Featuring Rod-Shaped Secondary Building Units.
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- Molecules, 2021, v. 26, n. 10, p. 2955, doi. 10.3390/molecules26102955
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Ligand-Targeted Delivery of Photosensitizers for Cancer Treatment.
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- Molecules, 2020, v. 25, n. 22, p. 5317, doi. 10.3390/molecules25225317
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Weak Interactions and Conformational Changes in Core-Protonated A2- and Ax-Type Porphyrin Dications.
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- Molecules, 2020, v. 25, n. 14, p. 3195, doi. 10.3390/molecules25143195
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Targeting Receptor Tyrosine Kinase VEGFR-2 in Hepatocellular Cancer: Rational Design, Synthesis and Biological Evaluation of 1,2-Disubstituted Benzimidazoles.
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- Molecules, 2020, v. 25, n. 4, p. 770, doi. 10.3390/molecules25040770
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Synthesis of Mono- and Disubstituted Porphyrins: A- and 5,10-A2-Type Systems.
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- Chemistry - A European Journal, 2005, v. 11, n. 11, p. 3427, doi. 10.1002/chem.200500001
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OxasmaragdyrinFerrocene and OxacorroleFerrocene Conjugates: Synthesis, Structure, and Nonlinear Optical Properties.
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- Chemistry - A European Journal, 2004, v. 10, n. 6, p. 1423
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The Reaction of Porphyrins with Organolithium Reagents.
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- Chemistry - A European Journal, 2000, v. 6, n. 15, p. 2721, doi. 10.1002/1521-3765(20000804)6:15<2721::AID-CHEM2721>3.0.CO;2-Z
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- Article
Thiourea Organocatalysts as Emerging Chiral Pollutants: En Route to Porphyrin-Based (Chir)Optical Sensing.
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- Chemosensors, 2021, v. 9, n. 10, p. 278, doi. 10.3390/chemosensors9100278
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Structural investigation of 5,10- A<sub>2</sub> B<sub>2</sub>-type porphyrins: palladium(II) and zinc(II) complexes of 5,10-dibromo-15,20-bis(4-methylphenyl)porphyrin.
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- Acta Crystallographica Section C: Structural Chemistry, 2014, v. 70, n. 12, p. 1143, doi. 10.1107/S2053229614023687
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Chlorophylls, Symmetry, Chirality, and Photosynthesis.
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- Symmetry (20738994), 2014, v. 6, n. 3, p. 781, doi. 10.3390/sym6030781
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Primary Processes of Photosynthesis. Principles and Apparatus. 2 Vols. Edited by Gernot Renger.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 37, p. 6944, doi. 10.1002/anie.200785593
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Metamorphosis of Tetrapyrrole Macrocycles.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 45, p. 7492, doi. 10.1002/anie.200603249
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The Photosensitizer Temoporfin (mTHPC) – Chemical, Pre‐clinical and Clinical Developments in the Last Decade<sup>†</sup><sup>‡</sup>.
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- Photochemistry & Photobiology, 2023, v. 99, n. 2, p. 356, doi. 10.1111/php.13730
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Spectroelectrochemical Investigation of the One-Electron Reduction of Nonplanar Nickel(II) Porphyrins.
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- ChemPhysChem, 2016, v. 17, n. 21, p. 3480, doi. 10.1002/cphc.201600698
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Porphyrins as Colorimetric and Photometric Biosensors in Modern Bioanalytical Systems.
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- ChemBioChem, 2020, v. 21, n. 13, p. 1793, doi. 10.1002/cbic.202000067
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Porphyrins as Colorimetric and Photometric Biosensors in Modern Bioanalytical Systems.
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- ChemBioChem, 2020, v. 21, n. 13, p. 1779, doi. 10.1002/cbic.202000352
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- Article