Works matching DE "ROTAXANES synthesis"
Results: 57
Synthesis, Photophysical, and Morphological Properties of Azomethine-Persylilated α-Cyclodextrin Main-Chain Polyrotaxane.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 6, p. 662, doi. 10.1002/macp.201400543
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Formation and Stability of Benzylic Amide [2]‐ and [3]Rotaxanes: An Intercomponent Interactions Study.
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- Chemistry - A European Journal, 2024, v. 30, n. 64, p. 1, doi. 10.1002/chem.202403276
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Modular Synthesis of Improbable Rotaxanes with All‐Benzene Scaffolds.
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- Angewandte Chemie, 2024, v. 136, n. 18, p. 1, doi. 10.1002/ange.202401838
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Ring‐to‐Thread Chirality Transfer in [2]Rotaxanes for the Synthesis of Enantioenriched Lactams.
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- Angewandte Chemie, 2022, v. 134, n. 39, p. 1, doi. 10.1002/ange.202209904
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Polyyne [3]Rotaxanes: Synthesis via Dicobalt Carbonyl Complexes and Enhanced Stability.
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- Angewandte Chemie, 2022, v. 134, n. 10, p. 1, doi. 10.1002/ange.202116897
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Rotaxanes as Cages to Control DNA Binding, Cytotoxicity, and Cellular Uptake of a Small Molecule.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 11023, doi. 10.1002/ange.202100151
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Syntheses of polyrotaxane conjugated with 5-fluorouracil and vitamins with improved antitumor activities.
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- Journal of Bioactive & Compatible Polymers, 2019, v. 34, n. 1, p. 25, doi. 10.1177/0883911518813617
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Mechanical Chirality of Rotaxanes: Synthesis and Function.
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- Symmetry (20738994), 2020, v. 12, n. 1, p. 144, doi. 10.3390/sym12010144
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Reversible Mechanical Switching of Magnetic Interactions in a Molecular Shuttle.
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- ChemistryOpen, 2015, v. 4, n. 1, p. 18, doi. 10.1002/open.201402073
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Solvent‐free synthesis of rotaxanes.
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- Journal of the Chinese Chemical Society, 2019, v. 66, n. 2, p. 134, doi. 10.1002/jccs.201800382
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Integrative Self‐Sorting: One‐Pot Synthesis of a Hetero[4]rotaxane from a Daisy‐Chain‐Containing Hetero[4]pseudorotaxane.
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- Chemistry - An Asian Journal, 2018, v. 13, n. 7, p. 815, doi. 10.1002/asia.201800011
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Four-State Molecular Shuttling of [2]Rotaxanes in Response to Acid/Base and Alkali-Metal Cation Stimuli.
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- Chemistry - An Asian Journal, 2017, v. 12, n. 12, p. 1381, doi. 10.1002/asia.201700493
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Selenoureido Calix[6]arenes: A Novel Platform for Pseudorotaxane Synthesis.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 27, p. 1, doi. 10.1002/ejoc.202400237
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Conjugated bis(enaminones) as effective templates for rotaxane assembly and their post-synthetic modifications.
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- Communications Chemistry, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42004-024-01258-4
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Cyclodextrin‐Based Rotaxanes: from Rotaxanes to Polyrotaxanes and Further to Functional Materials.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 21, p. 3344, doi. 10.1002/ejoc.201900090
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Conformer Distribution in Rotaxanes Containing Nonsymmetric Threads: A Systematic Approach.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 36, p. 4978, doi. 10.1002/ejoc.201800991
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Effects on Rotational Dynamics of Azo and Hydrazodicarboxamide-Based Rotaxanes.
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- Molecules, 2017, v. 22, n. 7, p. 1078, doi. 10.3390/molecules22071078
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Polyurethane‐Type Poly[3]rotaxanes Synthesized from Cyclodextrin‐Based [3]Rotaxane Diol and Diisocyanates.
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- Macromolecular Rapid Communications, 2024, v. 45, n. 20, p. 1, doi. 10.1002/marc.202400441
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Control over the Redox Cooperative Mechanism of Radical Carbene Transfer Reactions for the Efficient Active‐Metal‐Template Synthesis of [2]Rotaxanes.
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- Chemistry - A European Journal, 2020, v. 26, n. 35, p. 7808, doi. 10.1002/chem.201905602
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[2]Rotaxane End‐Capping Synthesis by Click Michael‐Type Addition to the Vinyl Sulfonyl Group.
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- Chemistry - A European Journal, 2019, v. 25, n. 24, p. 6170, doi. 10.1002/chem.201900156
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The Importance of Length and Flexibility of Macrocycle‐Containing Molecular Translocators for the Synthesis of Improbable [2]Rotaxanes.
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- Chemistry - A European Journal, 2018, v. 24, n. 51, p. 13659, doi. 10.1002/chem.201802831
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Redox‐Switchable Calix[6]arene‐Based Isomeric Rotaxanes.
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- Chemistry - A European Journal, 2018, v. 24, n. 47, p. 12370, doi. 10.1002/chem.201800496
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Construction of Crown Ether-Stoppering [3]Rotaxanes Based on N-Hetero Crown Ether Host.
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- Chinese Journal of Chemistry, 2017, v. 35, n. 7, p. 1050, doi. 10.1002/cjoc.201600878
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Front Cover: CuAAC in a Distal Pocket: Metal Active-Template Synthesis of Strapped-Porphyrin [2]Rotaxanes (Chem. Eur. J. 55/2017).
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- Chemistry - A European Journal, 2017, v. 23, n. 55, p. 13533, doi. 10.1002/chem.201703336
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CuAAC in a Distal Pocket: Metal Active-Template Synthesis of Strapped-Porphyrin [2]Rotaxanes.
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- Chemistry - A European Journal, 2017, v. 23, n. 55, p. 13537, doi. 10.1002/chem.201703337
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CuAAC in a Distal Pocket: Metal Active-Template Synthesis of Strapped-Porphyrin [2]Rotaxanes.
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- Chemistry - A European Journal, 2017, v. 23, n. 55, p. 13579, doi. 10.1002/chem.201702553
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Rotaxane-Like Structures Threaded through the Pores of Hollow Porous Nanocapusles.
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- Chemistry - A European Journal, 2016, v. 22, n. 40, p. 14137, doi. 10.1002/chem.201602731
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Rational Design for Rotaxane Synthesis through Intramolecular Slippage: Control of Activation Energy by Rigid Axle Length.
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- Chemistry - A European Journal, 2016, v. 22, n. 19, p. 6624, doi. 10.1002/chem.201600429
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Synthesis of [3]Rotaxanes that Utilize the Catalytic Activity of a Macrocyclic Phenanthroline-Cu Complex: Remarkable Effect of the Length of the Axle Precursor.
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- Chemistry - A European Journal, 2015, v. 21, n. 5, p. 2139, doi. 10.1002/chem.201405090
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A Halogen-Bonding Bis-triazolium Rotaxane for Halide-Selective Anion Recognition.
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- Chemistry - A European Journal, 2015, v. 21, n. 4, p. 1660, doi. 10.1002/chem.201405578
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Cyclodextrin-Based Size-Complementary [3]Rotaxanes: Selective Synthesis and Specific Dissociation.
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- Chemistry - A European Journal, 2014, v. 20, n. 51, p. 17132, doi. 10.1002/chem.201405005
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Rotaxanes Synthesized Through Sodium-Ion-Templated Clipping of Macrocycles Around Nonconjugated Amide and Urea Functionalities.
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- Chemistry - A European Journal, 2014, v. 20, n. 16, p. 4563, doi. 10.1002/chem.201400323
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Use of Cleavable Coordinating Rings as Protective Groups in the Synthesis of a Rotaxane with an Axis that Incorporates More Chelating Groups Than Threaded Macrocycles.
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- Chemistry - A European Journal, 2013, v. 19, n. 38, p. 12815, doi. 10.1002/chem.201301717
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Using 'Threading Followed by Shrinking' to Synthesize Highly Stable Dialkylammonium-Ion-Based Rotaxanes.
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- Chemistry - A European Journal, 2013, v. 19, n. 27, p. 8850, doi. 10.1002/chem.201300049
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Cyclic and Lasso Peptides: Sequence Determination, Topology Analysis, and Rotaxane Formation.
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- Angewandte Chemie, 2018, v. 130, n. 21, p. 6258, doi. 10.1002/ange.201801299
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Ring Shuttling Controls Macroscopic Motion in a Three-Dimensional Printed Polyrotaxane Monolith.
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- Angewandte Chemie, 2017, v. 129, n. 16, p. 4523, doi. 10.1002/ange.201612440
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A Simple and Highly Effective Ligand System for the Copper(I)-Mediated Assembly of Rotaxanes.
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- Angewandte Chemie, 2014, v. 126, n. 50, p. 13991, doi. 10.1002/ange.201407817
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Iodide-Induced Shuttling of a Halogen- and Hydrogen-Bonding Two-Station Rotaxane.
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- Angewandte Chemie, 2014, v. 126, n. 44, p. 12048, doi. 10.1002/ange.201407580
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Synthesis of dithioureado-bridged bis-pillar[5]arenes and formation of unique bis-[1]rotaxanes.
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- Supramolecular Chemistry, 2018, v. 30, n. 7, p. 642, doi. 10.1080/10610278.2018.1427238
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Shielded alkyl-functionalised rotaxane host cavities for improved anion recognition.
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- Supramolecular Chemistry, 2016, v. 28, n. 1/2, p. 62, doi. 10.1080/10610278.2015.1075538
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Guest-dependent complexation of triptycene-derived macrotricyclic host containing one anthracene moiety with paraquat derivatives: construction of [2]rotaxanes.
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- Supramolecular Chemistry, 2015, v. 27, n. 5/6, p. 357, doi. 10.1080/10610278.2014.976220
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Synthesis, characterisation and photoswitchability of a new [2]rotaxane of α-cyclodextrin with a diazobenzene containing π-conjugated molecular dumbbell.
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- Supramolecular Chemistry, 2012, v. 24, n. 5, p. 333, doi. 10.1080/10610278.2012.660529
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Synthetic Strategies for Oligoynes.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 4, p. 286, doi. 10.1002/ajoc.201402261
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Incorporation of Calix[6]Arene Macrocycles and (Pseudo)Rotaxanes in Bilayer Membranes: Towards Controllable Artificial Liposomal Channels.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 3, p. 262, doi. 10.1002/ajoc.201402244
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A Ferrocene-Functionalized Bistable [2]Rotaxane with Switchable Fluorescence.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 3, p. 221, doi. 10.1002/ajoc.201402155
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A Perylene-Bridged Switchable [3]Rotaxane Molecular Shuttle with a Fluorescence Output.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 3, p. 212, doi. 10.1002/ajoc.201402201
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Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20372-0
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Ru(II)Porphyrinate-based molecular nanoreactor for carbene insertion reactions and quantitative formation of rotaxanes by active-metal-template syntheses.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-20046-x
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A Cholesterol Containing pH-Sensitive Bistable [2]Rotaxane.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 27, p. 5966, doi. 10.1002/ejoc.201500657
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A Shuttle for the Transport of Protons Based on a [2]Rotaxane.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 18, p. 3885, doi. 10.1002/ejoc.201402249
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