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Polycationic Redox‐Active Cyclophanes with Integrated Electron‐Rich Diboron Units.
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- Chemistry - A European Journal, 2021, v. 27, n. 63, p. 15737, doi. 10.1002/chem.202102656
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Cover Feature: Controlling Regioselectivity in Palladium‐Catalyzed C−H Activation/Aryl–Aryl Coupling of 4‐Phenylamino[2.2]paracyclophane (Chem. Eur. J. 61/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 61, p. 13746, doi. 10.1002/chem.202004087
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Cover Feature: Enantioselective Synthesis of Polycyclic Aromatic Hydrocarbon (PAH)‐Based Planar Chiral Bent Cyclophanes by Rhodium‐Catalyzed [2+2+2] Cycloaddition (Chem. Eur. J. 55/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 55, p. 12492, doi. 10.1002/chem.202002761
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Enantioselective Synthesis of Polycyclic Aromatic Hydrocarbon (PAH)‐Based Planar Chiral Bent Cyclophanes by Rhodium‐Catalyzed [2+2+2] Cycloaddition.
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- Chemistry - A European Journal, 2020, v. 26, n. 55, p. 12579, doi. 10.1002/chem.202001450
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Cover Feature: Ratiometric Detection of ATP by Fluorescent Cyclophanes with Bellows‐Type Sensing Mechanism (Chem. Eur. J. 44/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 44, p. 9654, doi. 10.1002/chem.202003014
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Ratiometric Detection of ATP by Fluorescent Cyclophanes with Bellows‐Type Sensing Mechanism.
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- Chemistry - A European Journal, 2020, v. 26, n. 44, p. 9991, doi. 10.1002/chem.202001523
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- Article
One‐Step Synthesis of Cyclophanes as Crystalline Sponge and Their [2]Catenanes through S<sub>N</sub>Ar Reactions.
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- Chemistry - A European Journal, 2020, v. 26, n. 23, p. 5157, doi. 10.1002/chem.201905854
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Electron‐Rich, Lewis Acidic Diborane Meets N‐Heterocyclic Aromatics: Formation and Electron Transfer in Cyclophane Boranes.
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- Chemistry - A European Journal, 2020, v. 26, n. 15, p. 3435, doi. 10.1002/chem.202000189
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Distortion‐Controlled Redshift of Organic Dye Molecules.
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- Chemistry - A European Journal, 2020, v. 26, n. 9, p. 2080, doi. 10.1002/chem.201905355
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Anthracene‐Based Cyclophanes with Selective Fluorescent Responses for TTP and GTP: Insights into Recognition and Sensing Mechanisms.
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- Chemistry - A European Journal, 2019, v. 25, n. 14, p. 3541, doi. 10.1002/chem.201806130
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Aqueous Assembly of Zwitterionic Daisy Chains.
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- Chemistry - A European Journal, 2019, v. 25, n. 1, p. 285, doi. 10.1002/chem.201803944
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Total Synthesis of (−)‐Cylindrocyclophane F: A Yardstick for Probing New Catalytic C−C Bond‐Forming Methodologies.
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- Chemistry - A European Journal, 2018, v. 24, n. 63, p. 16770, doi. 10.1002/chem.201804585
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Dibenzo[a,e]pentalenophanes: Bending a Non‐Alternant Hydrocarbon.
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- Chemistry - A European Journal, 2018, v. 24, n. 29, p. 7374, doi. 10.1002/chem.201800322
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- Article
Polycationic Open‐Shell Cyclophanes: Synthesis of Electron‐Rich Chiral Macrocycles, and Redox‐Dependent Electronic States.
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- Angewandte Chemie, 2024, v. 136, n. 27, p. 1, doi. 10.1002/ange.202402800
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Enantioselective Synthesis of Planar‐Chiral Sulfur‐Containing Cyclophanes by Chiral Sulfide Catalyzed Electrophilic Sulfenylation of Arenes.
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- Angewandte Chemie, 2024, v. 136, n. 10, p. 1, doi. 10.1002/ange.202318625
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Palladium‐Catalyzed Enantioselective C−H Olefination to Access Planar‐Chiral Cyclophanes by Dynamic Kinetic Resolution.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202315603
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Stacking Cyclophanes into Chiral Microvessels.
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- Angewandte Chemie, 2023, v. 135, n. 16, p. 1, doi. 10.1002/ange.202214996
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The Story of the Little Blue Box: A Tribute to Siegfried Hünig.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202211387
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Rücktitelbild: Excited State Charge‐Transfer Complexes Enable Fluorescence Color Changes in a Supramolecular Cyclophane Mechanophore (Angew. Chem. 42/2022).
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- Angewandte Chemie, 2022, v. 134, n. 42, p. 1, doi. 10.1002/ange.202213675
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Aggregation‐Induced Emission and Circularly Polarized Luminescence Duality in Tetracationic Binaphthyl‐Based Cyclophanes.
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- Angewandte Chemie, 2022, v. 134, n. 40, p. 1, doi. 10.1002/ange.202208679
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A New Platform of B/N‐Doped Cyclophanes: Access to a π‐Conjugated Block‐Type B<sub>3</sub>N<sub>3</sub> Macrocycle with Strong Dipole Moment and Unique Optoelectronic Properties.
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- Angewandte Chemie, 2022, v. 134, n. 20, p. 1, doi. 10.1002/ange.202200612
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Benzidine/Quinoidal‐Benzidine‐Linked, Superbenzene‐Based π‐Conjugated Chiral Macrocycles and Cyclophanes.
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- Angewandte Chemie, 2020, v. 132, n. 24, p. 9814, doi. 10.1002/ange.202002447
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Innenrücktitelbild: Conformational Dynamics of Monomer‐ versus Dimer‐like Features in a Naphthalenediimide‐Based Conjugated Cyclophane (Angew. Chem. 13/2020).
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5445, doi. 10.1002/ange.202002169
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Conformational Dynamics of Monomer‐ versus Dimer‐like Features in a Naphthalenediimide‐Based Conjugated Cyclophane.
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5292, doi. 10.1002/ange.201914414
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Rational Development of Remote C−H Functionalization of Biphenyl: Experimental and Computational Studies.
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- Angewandte Chemie, 2020, v. 132, n. 12, p. 4800, doi. 10.1002/ange.201915624
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"Design of Experiments" as a Method to Optimize Dynamic Disulfide Assemblies: Cages and Functionalizable Macrocycles.
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- Angewandte Chemie, 2020, v. 132, n. 4, p. 1512, doi. 10.1002/ange.201912169
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Cyclotris(paraquat‐p‐phenylenes).
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- Angewandte Chemie, 2019, v. 131, n. 39, p. 13916, doi. 10.1002/ange.201907329
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Indeno[1,2‐b]fluorene‐Based [2,2]Cyclophanes with 4n/4n and 4n/[4n+2] π Electrons: Syntheses, Structural Analyses, and Excitonic Coupling Properties.
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- Angewandte Chemie, 2019, v. 131, n. 30, p. 10264, doi. 10.1002/ange.201903561
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Poly(arylenevinylene)s through Ring‐Opening Metathesis Polymerization of an Unsymmetrical Donor‐Acceptor Cyclophane.
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- Angewandte Chemie, 2019, v. 131, n. 28, p. 9627, doi. 10.1002/ange.201905137
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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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Computational Insight into the Rope-Skipping Isomerization of Diarylether Cyclophanes.
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- Symmetry (20738994), 2021, v. 13, n. 11, p. 2127, doi. 10.3390/sym13112127
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The Asymmetry is Derived from Mechanical Interlocking of Achiral Axle and Achiral Ring Components -Syntheses and Properties of Optically Pure [2]Rotaxanes-.
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- Symmetry (20738994), 2018, v. 10, n. 1, p. 20, doi. 10.3390/sym10010020
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Direct Synthesis of Polyaromatic Cyclophanes Containing Bis-Methylene-Interrupted Z -Double Bonds and Study of Their Antitumor Activity In Vitro.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 16, p. 8787, doi. 10.3390/ijms22168787
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The Role of Calix[n]arenes and Pillar[n]arenes in the Design of Silver Nanoparticles: Self-Assembly and Application.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1425, doi. 10.3390/ijms21041425
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Synthesis of tetramethoxy-(tetra-hydrazinecarboxamide) cyclophanes with unexpected conformation, and investigation of their solution-phase recognition of chiral carboxylic guests using time-of-flight and tandem mass spectrometry.
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- ARKIVOC: Online Journal of Organic Chemistry, 2015, v. 2015, p. 1, doi. 10.3998/ark.5550190.p008.875
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Donor-acceptor rotaxanes with tetracationic cyclophane ring.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 185
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Synthesis of thiophenophanes with ethyne and ethene spacers.
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 213
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Spectroscopic investigations of molecular association of cyclophanes with anthracene.
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- ARKIVOC: Online Journal of Organic Chemistry, 2010, p. 179
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- Article
4,15-Diamino[2.2]paracyclophane as a useful precursor for the synthesis of novel pseudo-geminal [2.2]paracyclophane compounds.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2015, v. 70, n. 11, p. 843, doi. 10.1515/znb-2015-0093
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- Article
"One Ring to Bind Them All"--Part I: The Efficiency of the Macrocyclic Scaffold for G-Quadruplex DNA Recognition.
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- Journal of Nucleic Acids, 2010, p. 1, doi. 10.4061/2010/525862
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C–H Activation of the 5‐(Pyridine‐3‐yloxy)isophthalic Acid to Construct Iridium, Rhodium, and Ruthenium Binuclear Metallocyclophanes.
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- Bulletin of the Korean Chemical Society, 2018, v. 39, n. 9, p. 1030, doi. 10.1002/bkcs.11543
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Supramolecular Competitive Host–Guest Interaction Induced Reversible Macromolecular Metamorphosis.
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- Macromolecular Rapid Communications, 2019, v. 40, n. 22, p. N.PAG, doi. 10.1002/marc.201900376
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Synthesis of novel cyclophane-type crown ethers from 2-methylindole.
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- Journal of Chemical Research, 2013, v. 37, n. 10, p. 596, doi. 10.3184/174751913X13784003492579
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Pyrolysis of dimethoxy[n.2]metacyclophanes: an intramolecular condensation reaction to give oxa[n.2.1](1,3,2)cyclophanes.
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- Journal of Chemical Research, 2012, v. 36, n. 3, p. 134, doi. 10.3184/174751912X13296759770106
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Nitrosonium complexes of [2.2]paracyclophane.
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- Russian Journal of Organic Chemistry, 2006, v. 42, n. 3, p. 406, doi. 10.1134/S1070428006030122
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Synthesis of bis-octaethylporphyrin cyclophane derivatives.
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- Russian Journal of Organic Chemistry, 2004, v. 40, n. 12, p. 1819, doi. 10.1007/s11178-005-0106-1
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Catalytic Cycloaminomethylation of Aminobenzamides with 1,3-Bis[dimethylamino(methoxy)methyl]thiourea.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 3, p. 378, doi. 10.1134/S1070363219030022
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Cyclophanes: Simulation of the formation enthalpy by quantum-chemical methods.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 5, p. 918, doi. 10.1134/S1070363217050048
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Phosphorylation of aminomethylated derivatives of 2,7-dihydroxynaphthalenes.
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- Russian Journal of General Chemistry, 2016, v. 86, n. 3, p. 544, doi. 10.1134/S1070363216030099
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1,3-Dihydroxynaphthalene in the Synthesis of Phosphorus-containing Macroheterocycles.
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- Russian Journal of General Chemistry, 2005, v. 75, n. 12, p. 1910, doi. 10.1007/s11176-006-0013-3
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