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Frontispiz: Chemodivergent Parallel Kinetic Resolution of Paracyclophanes: Enantiomer Fishing with Different Substrates.
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- Angewandte Chemie, 2024, v. 136, n. 46, p. 1, doi. 10.1002/ange.202484661
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Titelbild: Programmable Chemical Evolution with Natural/Non‐Natural Building Blocks (Angew. Chem. 46/2024).
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- Angewandte Chemie, 2024, v. 136, n. 46, p. 1, doi. 10.1002/ange.202416801
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Organic Room‐Temperature Phosphorescence with Strong Circularly Polarized Luminescence Based on Paracyclophanes.
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- Angewandte Chemie, 2019, v. 131, n. 48, p. 17380, doi. 10.1002/ange.201909076
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Contractive Annulation: A Strategy for the Synthesis of Small, Strained Cyclophanes and Its Application in the Synthesis of [2](6,1)Naphthaleno[1]paracyclophane.
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- Angewandte Chemie, 2019, v. 131, n. 27, p. 9264, doi. 10.1002/ange.201904673
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Homochiral [2.2]Paracyclophane Self-Assembly Promoted by Transannular Hydrogen Bonding.
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- Angewandte Chemie, 2016, v. 128, n. 36, p. 10884, doi. 10.1002/ange.201605286
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A small molecule screen identifies novel inhibitors of mechanosensory nematocyst discharge in Hydra.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-99974-7
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Crystal Structure Studies towards the Synthesis and Applications of N-heterocyclic Carbene-Metal Complexes Derived from [2.2]Paracyclophane.
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- Australian Journal of Chemistry, 2015, v. 68, n. 10, p. 1472, doi. 10.1071/CH15002
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Corrigendum: Homochiral [2.2]Paracyclophane Self-Assembly Promoted by Transannular Hydrogen Bonding.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 6, p. 1441, doi. 10.1002/anie.201610870
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Homochiral [2.2]Paracyclophane Self-Assembly Promoted by Transannular Hydrogen Bonding.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 36, p. 10726, doi. 10.1002/anie.201605286
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Cyclophanes Containing Bowl-Shaped Aromatic Chromophores: Three Isomers of anti-[2.2](1,4)Subphthalocyaninophane.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 17, p. 5187, doi. 10.1002/anie.201411510
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Efficient and Modular Synthesis of New Structurally Diverse Functionalized [ n]Paracyclophanes by a Ring-Distortion Strategy.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 33, p. 8705, doi. 10.1002/anie.201401070
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Anti-[2.2](1,4)pentacenophane: A Covalently Coupled Pentacene Dimer.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 44, p. 11647, doi. 10.1002/anie.201303649
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Cyclophanes, Part 73: diastereoselective dimerization of an α,β-unsaturated ketone. Structure of all-trans-1,3-dibenzoyl-2,4-di([2.2]paracyclophan-4-yl)cyclobutane.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2015, v. 70, n. 8, p. 573, doi. 10.1515/znb-2015-0022
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Charge density investigations on [2,2]-paracyclophane - in data we trust.
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- Acta Crystallographica Section B: Structural Science, Crystal Engineering & Materials, 2015, v. 71, n. 1, p. 10, doi. 10.1107/S2052520614026080
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Efficient and Modular Synthesis of New Structurally Diverse Functionalized [ n]Paracyclophanes by a Ring-Distortion Strategy.
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- Angewandte Chemie, 2014, v. 126, n. 33, p. 8849, doi. 10.1002/ange.201401070
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Electron density analysis of bent aromatic molecules: intramolecular interactions in small paracyclophanes.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 8, p. 1, doi. 10.1007/s00214-016-1960-3
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Absorption and Luminescence Properties of [2.2]Paracyclophane due to Strong Transannular Interaction.
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- Journal of Applied Spectroscopy, 2014, v. 81, n. 1, p. 49, doi. 10.1007/s10812-014-9885-x
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Kinetic resolution of substituted amido[2.2]paracyclophanes via asymmetric electrophilic amination.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40718-8
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Regioselective ortho‐Palladation of [2.2]Paracyclophane Scaffolds: Accessing Planar and Central Chiral N,C‐Palladacycles.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 36, p. 5090, doi. 10.1002/ejoc.202101066
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Regioselective Synthesis of 4,7,12,15‐Tetrasubstituted [2.2]Paracyclophanes: A Modular Route Involving Optical Resolution.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 34, p. 4828, doi. 10.1002/ejoc.202100762
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Para‐Functionalization of N‐Substituted 4‐amino[2.2]paracyclophanes by Regioselective Formylation.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 29, p. 4015, doi. 10.1002/ejoc.202100288
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Front Cover: Beyond Simple Substitution Patterns – Symmetrically Tetrasubstituted [2.2]Paracyclophanes as 3D Functional Materials (Eur. J. Org. Chem. 20/2019).
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 20, p. 3071, doi. 10.1002/ejoc.201900683
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Beyond Simple Substitution Patterns – Symmetrically Tetrasubstituted [2.2]Paracyclophanes as 3D Functional Materials.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 20, p. 3073, doi. 10.1002/ejoc.201900061
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Enantiopure planar chiral [2.2]paracyclophanes: Synthesis and applications in asymmetric organocatalysis.
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- Chirality, 2021, v. 33, n. 9, p. 506, doi. 10.1002/chir.23335
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Synthesis of enantiopure planar chiral bis‐(para)‐pseudo‐meta‐type [2.2]paracyclophanes.
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- Chirality, 2018, v. 30, n. 10, p. 1109, doi. 10.1002/chir.23010
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Tetrathiafulvalene‐[2.2]paracyclophanes: Synthesis, crystal structures, and chiroptical properties.
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- Chirality, 2018, v. 30, n. 5, p. 568, doi. 10.1002/chir.22831
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Synthesis of Mono‐, Di‐, Tri‐, and Tetra‐cationic Pyridinium and Vinylpyridinium Modified [2.2]Paracyclophanes: Modular Receptors for Supramolecular Systems.
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- ChemistryOpen, 2024, v. 13, n. 8, p. 1, doi. 10.1002/open.202400024
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Influence of Ag<sup>+</sup> on the Magnetic Response of [2.2.2]Paracyclophane: NMR Properties of a Prototypical Organic Host for Cation Binding Based on DFT Calculations.
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- ChemistryOpen, 2015, v. 4, n. 5, p. 651, doi. 10.1002/open.201500106
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[2.2]Paracyclophane-based single molecular wire consisting of four π-electron systems.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 4, p. 424, doi. 10.1139/cjc-2016-0526
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Donor–Donor′–Acceptor Triads Based on [3.3]Paracyclophane with a 1,4‐Dithiafulvene Donor and a Cyanomethylene Acceptor: Synthesis, Structure, and Electrochemical and Photophysical Properties.
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- Chemistry - A European Journal, 2018, v. 24, n. 44, p. 11407, doi. 10.1002/chem.201801774
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Unprecedented One-Pot Reaction towards Chiral, Non-Racemic Copper(I) Complexes of [2.2]Paracyclophane-Based P,N-Ligands.
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- Chemistry - A European Journal, 2017, v. 23, n. 65, p. 16452, doi. 10.1002/chem.201704115
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[2.2]Paracyclophane-Bis(triazole) Systems: Synthesis and Photochemical Behavior.
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- Chemistry - A European Journal, 2017, v. 23, n. 50, p. 12338, doi. 10.1002/chem.201701593
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Modulating the Bonding Properties of N-Heterocyclic Carbenes (NHCs): A Systematic Charge-Displacement Analysis.
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- Chemistry - A European Journal, 2017, v. 23, n. 31, p. 7558, doi. 10.1002/chem.201700638
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Optically Active Phenylethene Dimers Based on Planar Chiral Tetrasubstituted [2.2]Paracyclophane.
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- Chemistry - A European Journal, 2017, v. 23, n. 26, p. 6323, doi. 10.1002/chem.201605598
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Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes.
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- Chemistry - A European Journal, 2017, v. 23, n. 26, p. 6315, doi. 10.1002/chem.201605237
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Back Cover: Optically Active Phenylethene Dimers Based on Planar Chiral Tetrasubstituted [2.2]Paracyclophane (Chem. Eur. J. 26/2017).
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- Chemistry - A European Journal, 2017, v. 23, n. 26, p. 6460, doi. 10.1002/chem.201700693
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Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017).
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- Chemistry - A European Journal, 2017, v. 23, n. 26, p. 6459, doi. 10.1002/chem.201700517
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Macrocyclic Oligothiophene with Stereogenic [2.2]Paracyclophane Scaffolds: Chiroptical Properties from π-Transannular Interactions.
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- Chemistry - A European Journal, 2017, v. 23, n. 14, p. 3267, doi. 10.1002/chem.201605842
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Enantioselective Synthesis of Planar‐Chiral Macrocycles through Asymmetric Electrophilic Aromatic Amination.
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- Angewandte Chemie, 2022, v. 134, n. 22, p. 1, doi. 10.1002/ange.202201064
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The truth is out there: the metal-π interactions in crystal of Cr(CO)<sub>3</sub>(pcp) as revealed by the study of vibrational smearing of electron density.
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- Zeitschrift für Kristallographie. Crystalline Materials, 2018, v. 233, n. 5, p. 317, doi. 10.1515/zkri-2017-2085
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Fourfold Alkoxy-Substituted [2.2.2]Paracyclophane-1,9,17-trienes-ROMP into PPVs with Unusual Topologies.
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- Macromolecular Rapid Communications, 2014, v. 35, n. 24, p. 2096, doi. 10.1002/marc.201400515
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π-Stacked Polymer Consisting of a Pseudo–meta–[2.2]Paracyclophane Skeleton.
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- Polymers (20734360), 2018, v. 10, n. 10, p. 1140, doi. 10.3390/polym10101140
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Planar-Chiral [2.2]Paracyclophane-Based Amides as Proligands for Titanium- and Zirconium-Catalyzed Hydroamination.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 13, p. 1760, doi. 10.1002/ejoc.201700101
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Highly Emissive Optically Active Conjugated Dimers Consisting of a Planar Chiral [2.2]Paracyclophane Showing Circularly Polarized Luminescence.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 35, p. 7756, doi. 10.1002/ejoc.201501181
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A Modular Synthesis of Multidentate S-, N- and O-Containing Meta- and Paracyclophanes.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 32, p. 6988, doi. 10.1002/ejoc.201501058
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Kinetic Resolution of a Planar-Chiral [2.2]Paracyclophane Derivative by Helical-Peptide-Catalyzed Michael Addition of Nitromethane (Eur. J. Org. Chem. 23/2015).
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 23, p. n/a, doi. 10.1002/ejoc.201590064
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Photochromism of Acetyl-Cyclophanochromene: Intriguing Stabilization of Photogenerated Colored o-Quinonoid Intermediates.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 7, p. 1403, doi. 10.1002/ejoc.201403403
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Synthesis of Bromo-Substituted 4-Hydroxy[2.2]paracyclophanes and [2.2]Paracyclophane-4,7-quinones as Versatile Chiral Building Blocks.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 2, p. 325, doi. 10.1002/ejoc.201403316
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Roadmap towards N-Heterocyclic [2.2]Paracyclophanes and Their Application in Asymmetric Catalysis.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 27, p. 6108, doi. 10.1002/ejoc.201300508
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Synthesis, Chiral Resolution, and Absolute Configuration of Dissymmetric 4,12-Difunctionalized [2.2]Paracyclophanes.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 21, p. 4523, doi. 10.1002/ejoc.201300412
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