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Synthesis of Disubstituted Cucurbit[6]uril and Its Rotaxane Derivative
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20001201)39:23<4257::aid-anie4257>3.0.co;2-6openalex-snapshot
Ternary Complexes Between DNA, Polyamine, and Cucurbituril: A Modular Approach to DNA-Binding Molecules
inferredcites →https://doi.org/10.1002/1521-3773(20001201)39:23<4260::aid-anie4260>3.0.co;2-9openalex-snapshot
Complexation of Antimony(III) by Trypanothione
inferredcites →https://doi.org/10.1002/1521-3773(20010917)40:18<3364::aid-anie3364>3.0.co;2-sopenalex-snapshot
Atomic Force Microscope Studies on Condensation of Plasmid DNA with Functionalized Fullerenes
inferredcites →https://doi.org/10.1002/1521-3773(20010917)40:18<3367::aid-anie3367>3.0.co;2-aopenalex-snapshot
Zero-Strain Intercalation Cathode for Rechargeable Li-Ion Cell
inferredcites →https://doi.org/10.1002/1521-3773(20011119)40:22<4235::aid-anie4235>3.0.co;2-1openalex-snapshot
Self-Assembly of a Mixed-Valence Copper(II)/Copper(III) Dithiocarbamate Catenane
inferredcites →https://doi.org/10.1002/jlac.19053390102openalex-snapshot
I. Ueber Condensationsproducte aus Glycoluril und Formaldehyd
inferredcites →https://doi.org/10.1016/s0166-1280(98)00286-3openalex-snapshot
A proton NMR shielding model for the face of a benzene ring
inferredcites →https://doi.org/10.1021/ja00414a071openalex-snapshot
Successive Beckmann rearrangement-alkylation sequence by organoaluminum reagents. Simple route to dl-pumiliotoxin C
inferredcites →https://doi.org/10.1023/a:1011184725796openalex-snapshot
Cucurbit[5]uril, Decamethylcucurbit[5]uril and Cucurbit[6]uril. Synthesis, Solubility and Amine Complex Formation
inferredcites →https://doi.org/10.5860/choice.34-5097openalex-snapshot
Comprehensive supramolecular chemistry
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4743861openalex-extracted
Preparation of a Class of Cucurbit[6]Uril-Light Rare-Earth- Based Supramolecular Assemblies and its Efficient Detection of Chloramphenicol
inferred← citeshttps://doi.org/10.2139/ssrn.4862668openalex-extracted
Preparation of a Class of Cucurbit[5]Uril- Ln3+- Based Supramolecular Assemblies and its Efficient Detection of L-Tryptophan
inferred← citeshttps://doi.org/10.1002/9780470661345.smc056openalex-snapshot
Cucurbituril Receptors and Drug Delivery
inferred← citeshttps://doi.org/10.1002/9781119053859.ch6openalex-snapshot
Robust Host–Guest Chemistry of Cucurbit[ n ]uril
inferred← citeshttps://doi.org/10.1002/ange.202002666openalex-snapshot
Cucurbit[ n ]uril‐Based Supramolecular Frameworks Assembled through Outer‐Surface Interactions
inferred← citeshttps://doi.org/10.1002/anie.202002666openalex-snapshot
Cucurbit[ n ]uril‐Based Supramolecular Frameworks Assembled through Outer‐Surface Interactions
inferred← citeshttps://doi.org/10.1002/chem.200601657openalex-snapshot
Face‐Selective [2]‐ and [3]Rotaxanes: Kinetic Control of the Threading Direction of Cyclodextrins
inferred← citeshttps://doi.org/10.1002/chem.200601830openalex-snapshot
Nitroxide Radicals as Probes for Exploring the Binding Properties of the Cucurbit[7]uril Host
inferred← citeshttps://doi.org/10.1002/chem.200701531openalex-snapshot
Infrared Study of Intercomponent Interactions in a Switchable Hydrogen‐Bonded Rotaxane
inferred← citeshttps://doi.org/10.1002/chem.202004711openalex-snapshot
Potential Applications of Cucurbit[n]urils and Their Derivatives in the Capture of Hazardous Chemicals
inferred← citeshttps://doi.org/10.1002/ejoc.201300229openalex-snapshot
Synthesis of Cucurbit[6]uril Derivatives and Insights into Their Solubility in Water
inferred← citeshttps://doi.org/10.1002/jhet.4738openalex-snapshot
Synthesis and DFT calculations of mono‐ and di‐methylated cucurbit[7]uril based on imidazole derivatives
inferred← citeshttps://doi.org/10.1002/jms.978openalex-snapshot
Characterization of host–guest complexes of cucurbit[n]uril (n = 6, 7) by electrospray ionization mass spectrometry
inferred← citeshttps://doi.org/10.1002/qua.25877openalex-snapshot
Formation of aqua and tetraammine Cu(II) complexes inside the cavities of cucurbit[6,8]urils: A DFT forecast
inferred← citeshttps://doi.org/10.1002/slct.202202520openalex-snapshot
Supramolecular Self‐Assembly Modes of Cyclopentanocucurbit[6]uril and Aromatic Amines
inferred← citeshttps://doi.org/10.1007/978-3-662-08439-7_3openalex-snapshot
Cucurbituril: A Versatile “Bead” for Polyrotaxane Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-662-46629-2_1openalex-snapshot
Cucurbit[n]uril Chemistry
inferred← citeshttps://doi.org/10.1007/978-981-13-1744-6_34-1openalex-snapshot
Cucurbiturils-Based Pseudorotaxanes and Rotaxanes
inferred← citeshttps://doi.org/10.1007/978-981-15-2686-2_34openalex-snapshot
Cucurbiturils-Based Pseudorotaxanes and Rotaxanes
inferred← citeshttps://doi.org/10.1007/s10847-003-8835-7openalex-snapshot
Cucurbiturils?a New Family of Host Molecules
inferred← citeshttps://doi.org/10.1007/s10847-004-6472-4openalex-snapshot
Construction of Pseudorotaxanes and Rotaxanes Based on Cucurbit[n]uril
inferred← citeshttps://doi.org/10.1007/s10847-004-8835-7openalex-snapshot
Cucurbiturils?a New Family of Host Molecules
inferred← citeshttps://doi.org/10.1007/s10847-005-9027-4openalex-snapshot
Unexpected Cyclization of Dipyridyl-glycoluril in the Presence of Formaldehyde and Strong Acid: A New Scaffold with a Potential as an Anion Receptor
inferred← citeshttps://doi.org/10.1007/s10847-009-9544-7openalex-snapshot
Host–guest complexes of some cucurbit[n]urils with the hydrochloride salts of some imidazole derivatives
inferred← citeshttps://doi.org/10.1007/s10847-009-9553-6openalex-snapshot
Host–guest complexes of some cucurbit[n]urils with the hydrochloride salts of some imidazole derivatives
inferred← citeshttps://doi.org/10.1007/s10847-017-0751-3openalex-snapshot
Water structuring inside the cavities of cucurbit[n]urils (n = 5–8): a quantum-chemical forecast
inferred← citeshttps://doi.org/10.1007/s10847-018-0828-7openalex-snapshot
Self-assembled (pseudo)rotaxane and polyrotaxane through host–guest chemistry based on the cucurbituril family
inferred← citeshttps://doi.org/10.1007/s10847-020-00999-8openalex-snapshot
Cucurbiturils for environmental and analytical chemistry
inferred← citeshttps://doi.org/10.1007/s11426-009-0089-9openalex-snapshot
Host-guest complexes of a water soluble cucurbit[6]uril derivative with some dications of 1,ω-alkyldipyridines: 1H NMR and X-ray structures
inferred← citeshttps://doi.org/10.1007/s12039-024-02285-3openalex-snapshot
A nano-molar sensitive fluorescence sensor for cucurbit[7]uril
inferred← citeshttps://doi.org/10.1007/s40242-021-1045-2openalex-snapshot
Host-Guest Interactions of Cyclopentanocucurbit[6]uril with Alkyl Imidazolium Hydrochlorides
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12477-1openalex-snapshot
Cucurbit[ n ]urils
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12514-4openalex-snapshot
Cucurbiturils: Synthesis, Structures, Formation Mechanisms, and Nomenclature
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.12.003openalex-snapshot
Dimensional effects of organic anion templates in modulating the assembly of water clusters in cucurbit[6]uril supramolecular systems
inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213741openalex-snapshot
Cucurbit[n]uril/metal ion complex-based frameworks and their potential applications
inferred← citeshttps://doi.org/10.1016/j.ica.2021.120669openalex-snapshot
Metal-induced different structures of four cyclopentanocucurbit[5]uril-based complexes
inferred← citeshttps://doi.org/10.1016/j.molliq.2019.111085openalex-snapshot
Theoretical study on alkaloid encapsulating via monohydroxy-cucurbit[n]uril (n = 8,10)/graphene oxide composite
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.05.017openalex-snapshot
Synthesis of partially methyl substituted cucurbit[n]urils with 3a-methyl-glycoluril
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.05.031openalex-snapshot
Structures of supramolecular assemblies formed by substituted cucurbiturils and metal ions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.07.007openalex-snapshot
Crystal structures of host–guest complexes of meta-tricyclohexyl cucurbit[6]uril with small organic molecules
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.09.025openalex-snapshot
Structures of supramolecular assemblies formed by some partial substituted cucurbiturils and some metal ion complexes
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.11.029openalex-snapshot
Interaction models of three alkyl substituted cucurbit[6]urils with a hydrochloride salt of 4,4′-dipyridyl guest
inferred← citeshttps://doi.org/10.1016/j.molstruc.2008.03.045openalex-snapshot
Host–guest inclusion complexes of four partial alkyl-substituted cucurbit[6]urils with some probe guests
inferred← citeshttps://doi.org/10.1016/j.molstruc.2008.10.057openalex-snapshot
Crystal structures of three partially cyclopentano-substituted cucurbit[6]urils
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.04.022openalex-snapshot
Molecular capsules formed by three different cucurbit[5]urils and some lanthanide ions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.05.005openalex-snapshot
Crystal structures of three host–guest complexes of methylsubstituted cucurbit[6]urils and anthracene derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.06.006openalex-snapshot
Crystal structures of four host–guest inclusion complexes of α,α′,δ,δ′-tetramethylcucurbit[6]uril and cucurbit[8]uril with some l-amino acids
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.11.049openalex-snapshot
Supramolecular assemblies of host–guest complexes of cucurbit[6]uril with some organic molecules
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.05.039openalex-snapshot
Syntheses, crystal structures and physico-chemical properties of supramolecular assemblies based on cucurbit[6]uril and mono- and polynuclear bismuth(III) and mercury(II) halides
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136937openalex-snapshot
Supramolecular self-assembly between cyclopentanocucurbit[6]uril and 1H-benzotriazole
inferred← citeshttps://doi.org/10.1016/j.poly.2024.117044openalex-snapshot
Preparation of a class of cucurbit[6]uril-light rare-earth-based supramolecular assemblies and its efficient detection of chloramphenicol
inferred← citeshttps://doi.org/10.1016/j.tet.2011.08.097openalex-snapshot
1,6-Dibenzylglycoluril for synthesis of deprotected glycoluril dimer
inferred← citeshttps://doi.org/10.1016/j.tet.2013.12.047openalex-snapshot
Synthesis of a symmetrical octamethyl-substituted cucurbituril with a dimethyl-substituted glycoluril dimer
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130488openalex-snapshot
A water soluble tetramethyl-substituted cucurbit[8]uril obtained from larger intermediates?
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132409openalex-snapshot
Synthesis of symmetric dicyclohexanocucurbit[6]uril and its interaction with glycine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.06.110openalex-snapshot
Synthesis and binding behaviors of monomethyl cucurbit[6]uril
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00150-9openalex-snapshot
Preparation of glycoluril monomers for expanded cucurbit[n]uril synthesis
inferred← citeshttps://doi.org/10.1016/s1874-6004(05)80026-7openalex-snapshot
Chapter 3 From methylene bridged glycoluril dimers to cucurbit[n]uril analogs with some detours along the way
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02813openalex-snapshot
Molecular Snuggle and Stretch of a Tetraammonium Chain in the Construction of a Hetero-[4]pseudorotaxane with CyclopentanoQ[6] and Classical Q[7]
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04403openalex-snapshot
Arene-Cucurbiturils: Benzene-Containing Cucurbituril[2,4] and Benzene-Containing Cucurbituril[3,6]
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01786openalex-snapshot
The Inheritance Angle: A Determinant for the Number of Members in the Substituted Cucurbit[n]uril Family
inferred← citeshttps://doi.org/10.1021/acsabm.0c01061openalex-snapshot
Cucurbituril-Oriented Nanoplatforms in Biomedical Applications
inferred← citeshttps://doi.org/10.1021/ar020254kopenalex-snapshot
Cucurbituril Homologues and Derivatives: New Opportunities in Supramolecular Chemistry
inferred← citeshttps://doi.org/10.1021/cg201173jopenalex-snapshot
Cucurbit[n]urils (n= 5–8): A Comprehensive Solid State Study
inferred← citeshttps://doi.org/10.1021/cg400227kopenalex-snapshot
A Dihalide–Decahydrate Cluster of [X2(H2O)10]2– in a Supramolecular Architecture of {[Na2(H2O)6(H2O@TMEQ[6])]·2(C6H5NO3)}X2(H2O)10 (TMEQ[6] = α,α′,δ,δ′-Tetramethylcucurbit[6]uril; X = Cl, Br)
inferred← citeshttps://doi.org/10.1021/ci400175fopenalex-snapshot
Enumeration of Virtual Libraries of Combinatorial Modular Macrocyclic (Bracelet, Necklace) Architectures and Their Linear Counterparts
inferred← citeshttps://doi.org/10.1021/ic200109sopenalex-snapshot
Difference of Coordination between Alkali- and Alkaline-Earth-Metal Ions to a Symmetrical α,α′,δ,δ′-Tetramethylcucurbit[6]uril
inferred← citeshttps://doi.org/10.1021/ic200902gopenalex-snapshot
Novel Supramolecular Assemblies Based on Coordination of Samarium Cation to Cucurbit[5]uril
inferred← citeshttps://doi.org/10.1021/ja025876fopenalex-snapshot
Diastereoselective Formation of Glycoluril Dimers: Isomerization Mechanism and Implications for Cucurbit[n]uril Synthesis
inferred← citeshttps://doi.org/10.1021/ja0319846openalex-snapshot
Mechanism of Host−Guest Complexation by Cucurbituril
inferred← citeshttps://doi.org/10.1021/ja036536copenalex-snapshot
Facile Synthesis of Cucurbit[n]uril Derivatives via Direct Functionalization: Expanding Utilization of Cucurbit[n]uril
inferred← citeshttps://doi.org/10.1021/ja056988kopenalex-snapshot
The Inverted Cucurbit[n]uril Family
inferred← citeshttps://doi.org/10.1021/ja064323sopenalex-snapshot
Sequence-Specific Recognition and Cooperative Dimerization of N-Terminal Aromatic Peptides in Aqueous Solution by a Synthetic Host
inferred← citeshttps://doi.org/10.1021/ja900306mopenalex-snapshot
Probing Cucurbituril Assemblies in Water with TEMPO-like Nitroxides: A Trinitroxide Supraradical with Spin−Spin Interactions
inferred← citeshttps://doi.org/10.1021/jacs.5b04553openalex-snapshot
Comprehensive Synthesis of Monohydroxy–Cucurbit[ n ]urils ( n = 5, 6, 7, 8): High Purity and High Conversions
inferred← citeshttps://doi.org/10.1021/jacs.9b09639openalex-snapshot
Superacid-Mediated Functionalization of Hydroxylated Cucurbit[n]urils
inferred← citeshttps://doi.org/10.1021/jo0258958openalex-snapshot
Methylene-Bridged Glycoluril Dimers: Synthetic Methods
inferred← citeshttps://doi.org/10.1021/jo034399wopenalex-snapshot
Acyclic Congener of Cucurbituril: Synthesis and Recognition Properties
inferred← citeshttps://doi.org/10.1021/jo051655ropenalex-snapshot
Cucurbit[n]uril Analogues: Synthetic and Mechanistic Studies
inferred← citeshttps://doi.org/10.1021/jo100186qopenalex-snapshot
Reasons Why Aldehydes Do Not Generally Participate in Cucurbit[n]uril Forming Reactions
inferred← citeshttps://doi.org/10.1021/jp066031jopenalex-snapshot
Interaction between Tetramethylcucurbit[6]uril and Some Pyridine Derivates
inferred← citeshttps://doi.org/10.1021/jp107289sopenalex-snapshot
Electronic Structure and 1 H NMR Chemical Shifts in Host-Guest Complexes of Cucurbit[6]uril and sym-Tetramethyl Cucurbit[6]uril with Imidazole Derivatives
inferred← citeshttps://doi.org/10.1021/jp9059906openalex-snapshot
Remarkable Salt Effect on Stability of Supramolecular Complex between Modified Cucurbit[6]uril and Methylviologen in Aqueous Media
inferred← citeshttps://doi.org/10.1021/ma034294vopenalex-snapshot
Catalytic Self-Threading: A New Route for the Synthesis of Polyrotaxanes
inferred← citeshttps://doi.org/10.1021/ol0499755openalex-snapshot
Facile Purification of Rare Cucurbiturils by Affinity Chromatography
inferred← citeshttps://doi.org/10.1021/ol100883kopenalex-snapshot
Syntheses of Copillar[5]arenes by Co-oligomerization of Different Monomers
inferred← citeshttps://doi.org/10.1021/ol401766aopenalex-snapshot
New Chiral Cyclohexylhemicucurbit[6]uril
inferred← citeshttps://doi.org/10.1021/ol500828kopenalex-snapshot
Cucurbiturils Substituted on the Methylene Bridge
inferred← citeshttps://doi.org/10.1038/s43586-026-00495-2openalex-snapshot
Cucurbit[n]uril-type molecular containers
inferred← citeshttps://doi.org/10.1039/9781788015950-00007openalex-snapshot
Cucurbituril Homologues and Derivatives: Syntheses and Functionalization
inferred← citeshttps://doi.org/10.1039/9781788015967-00015openalex-snapshot
Synthesis of the Cucurbituril Family
inferred← citeshttps://doi.org/10.1039/9781788015967-00054openalex-snapshot
Cucurbituril Properties and the Thermodynamic Basis of Host–Guest Binding
inferred← citeshttps://doi.org/10.1039/9781849737821-00164openalex-snapshot
Cucurbiturils in Drug Delivery And For Biomedical Applications
inferred← citeshttps://doi.org/10.1039/b417999dopenalex-snapshot
Supramolecular modulation of action of polyamine on enzyme/DNA interactions
inferred← citeshttps://doi.org/10.1039/b603088mopenalex-snapshot
Functionalized cucurbiturils and their applications
inferred← citeshttps://doi.org/10.1039/b711285hopenalex-snapshot
Highly symmetric columnar channels in metal-free cucurbit[n]uril hydrate crystals (n = 6, 8)
inferred← citeshttps://doi.org/10.1039/b719927aopenalex-snapshot
A general and efficient method to form self-assembled cucurbit[n]uril monolayers on gold surfaces
inferred← citeshttps://doi.org/10.1039/b908490hopenalex-snapshot
Exclusion complexes of the HCl salts of benzidine and bis(4-aminophenyl) methane with two methyl-substituted cucurbiturils
inferred← citeshttps://doi.org/10.1039/c1ce05048fopenalex-snapshot
Hydroquinone-induced framework based on direct coordination of rubidium ions to cucurbit[7]uril
inferred← citeshttps://doi.org/10.1039/c1ra00768hopenalex-snapshot
Cucurbituril chemistry: a tale of supramolecular success
inferred← citeshttps://doi.org/10.1039/c3ce26491bopenalex-snapshot
An approach to networks based on coordination of alkyl-substituted cucurbit[5]urils and potassium ions
inferred← citeshttps://doi.org/10.1039/c3cs60261copenalex-snapshot
Cucurbit[n]uril-based coordination chemistry: from simple coordination complexes to novel poly-dimensional coordination polymers
inferred← citeshttps://doi.org/10.1039/c4cc09900aopenalex-snapshot
A cucurbit[5]uril analogue from dimethylpropanediurea–formaldehyde condensation
inferred← citeshttps://doi.org/10.1039/c4cs00273copenalex-snapshot
Cucurbiturils: from synthesis to high-affinity binding and catalysis
inferred← citeshttps://doi.org/10.1039/c5cc00236bopenalex-snapshot
Hydrophobic monofunctionalized cucurbit[7]uril undergoes self-inclusion complexation and forms vesicle-type assemblies
inferred← citeshttps://doi.org/10.1039/c5cc02216aopenalex-snapshot
A hybrid organic–inorganic molecular daisy chain
inferred← citeshttps://doi.org/10.1039/c5cs00631gopenalex-snapshot
Can we beat the biotin–avidin pair?: cucurbit[7]uril-based ultrahigh affinity host–guest complexes and their applications
inferred← citeshttps://doi.org/10.1039/c5nj00255aopenalex-snapshot
Supramolecular assembly of a methyl-substituted cucurbit[6]uril and its potential applications in selective sorption
inferred← citeshttps://doi.org/10.1039/c5ra03418copenalex-snapshot
Direct synthesis of cucurbit[5]uril-anchored polyacrylic acid microspheres and potential applications in selective sorption
inferred← citeshttps://doi.org/10.1039/c5ra09064dopenalex-snapshot
Direct syntheses of cucurbit[7]uril-anchored polyacrylic acid microspheres and adsorption of basic dyes by the derivative
inferred← citeshttps://doi.org/10.1039/c6ob00268dopenalex-snapshot
Synthesis and separation of cucurbit[n]urils and their derivatives
inferred← citeshttps://doi.org/10.1039/c7nj01669gopenalex-snapshot
Template-directed synthesis of cucurbituril analogues using propanediurea as a building block
inferred← citeshttps://doi.org/10.1039/d0ra09074copenalex-snapshot
Host–guest modes and supramolecular frameworks of complexes of tetramethyl cucurbit[6]uril with 4-chloroaniline and 4,4′-diaminostilbene
inferred← citeshttps://doi.org/10.1039/d2qi00513aopenalex-snapshot
Construction of cucurbit[ n ]uril-based supramolecular frameworks via host–guest inclusion and functional properties thereof
inferred← citeshttps://doi.org/10.1039/d2ra02459dopenalex-snapshot
Study on the coordination of cyclopentanocucurbit[5,6]uril with Fe 3+ , Co 2+ and Ni 2+ ions
inferred← citeshttps://doi.org/10.1039/d3ra07810hopenalex-snapshot
Study on the host–guest interactions between tetramethyl cucurbit[6]uril and 2-heterocyclic-substituted benzimidazoles
inferred← citeshttps://doi.org/10.1071/ch19400openalex-snapshot
The Host–Guest Properties Observed Between the Viologens and Cyclopentanocucurbit[6]uril
inferred← citeshttps://doi.org/10.1080/10610270701218570openalex-snapshot
Inclusion Interactions of Cucurbit[7]uril with Adenine and its Derivatives
inferred← citeshttps://doi.org/10.1080/10610270701457970openalex-snapshot
Host–guest Complex of a Water-soluble Cucurbit[6]uril Derivative with the Hydrochloride Salt of 3-amino-5-phenylpyrazole
inferred← citeshttps://doi.org/10.1080/10610270701666018openalex-snapshot
Cucurbit[n]urils (n=7, 8) binding of camptothecin and the effects on solubility and reactivity of the anticancer drug
inferred← citeshttps://doi.org/10.1080/10610270701747602openalex-snapshot
Opposing substitution in cucurbit[6]urils forms ellipsoid cavities: the symmetrical dicyclohexanocucurbit[6]uril is no exception highlighted by inclusion and exclusion complexes
inferred← citeshttps://doi.org/10.1080/10610270903410496openalex-snapshot
Electrically insulated molecular wires
inferred← citeshttps://doi.org/10.1080/10610278.2010.510187openalex-snapshot
Kinetic and thermodynamic inclusion complexes of symmetric teramethyl-substituted cucurbit[6]uril with HCl salts of N,N′-bis(pyridylmethyl)-1,6-hexanediamine
inferred← citeshttps://doi.org/10.1080/10610278.2011.563856openalex-snapshot
Host–guest interactions of 6-benzyladenine with normal and modified cucurbituril: 1H NMR, UV absorption spectroscopy and phase solubility methods
inferred← citeshttps://doi.org/10.1080/10610278.2014.910601openalex-snapshot
Molecular dynamics simulation study of the structural features and inclusion capacities of cucurbit[6]uril derivatives in aqueous solutions
inferred← citeshttps://doi.org/10.1080/10610278.2014.926362openalex-snapshot
New homologues of chiral cyclohexylhemicucurbit[n]urils
inferred← citeshttps://doi.org/10.1080/10610278.2014.936866openalex-snapshot
The influence of equatorial substitution and K+ ion concentration: an encapsulation study of CH4, CH3F, CH3Cl, CH2F2 and CF4, in Q[5], CyP5Q[5] and a CyP5Q[5]-carboxylate derivative
inferred← citeshttps://doi.org/10.1098/rsos.202120openalex-snapshot
The binding behaviours between cyclopentanocucurbit[6]uril and three amino acids
inferred← citeshttps://doi.org/10.1098/rsos.211280openalex-snapshot
Study on the host–guest complex of dicyclohexanocucurbit[6]uril and 2-phenylbenzimidazole, and its recognition effect toward Fe 3+
inferred← citeshttps://doi.org/10.1134/s1063774520070275openalex-snapshot
A Ternary Supramolecular Self-Assembly Model Based on Cyclopentano Cucurbit[5]uril
inferred← citeshttps://doi.org/10.1134/s1070428021120149openalex-snapshot
Synthesis of Glycoluril using Urea Phosphate
inferred← citeshttps://doi.org/10.1163/156855503321127529openalex-snapshot
Glycoluril derivatives as precursors in the preparation of substituted cucurbit[n]urils
inferred← citeshttps://doi.org/10.1246/cl.2012.972openalex-snapshot
A Facile Chromatographic Method for Purification of Pinacol Boronic Esters
inferred← citeshttps://doi.org/10.1360/04wb0031openalex-snapshot
Synthesis of a symmetrical tetrasubstituted cucurbit[6]uril and its host-guest inclusion complex with 2,2?-bipyridine
inferred← citeshttps://doi.org/10.1360/zb2009-39-3-281openalex-snapshot
水溶性六元瓜环衍生物与1,ω-亚烷基吡啶主客体配合物的1H NMR及晶体结构
inferred← citeshttps://doi.org/10.14233/ajchem.2022.23813openalex-snapshot
Liquid-Liquid Extraction and Transport of Amino Acids through Membrane by Cucurbit[6]uril and its Derivatives
inferred← citeshttps://doi.org/10.1515/gps-2021-0074openalex-snapshot
A study on the coordination of cyclohexanocucurbit[6]uril with copper, zinc, and magnesium ions
inferred← citeshttps://doi.org/10.1584/jpestics.w21-32openalex-snapshot
Crystalline materials with functional nanopores
inferred← citeshttps://doi.org/10.21203/rs.3.rs-25677/v1openalex-snapshot
The Binding Behaviors between Cyclopentanocucurbit[6]uril and Three Amino Acids in the Solid and the Solution Phases
inferred← citeshttps://doi.org/10.21203/rs.3.rs-25677/v2openalex-snapshot
The Binding Behaviors between Cyclopentanocucurbit[6]uril and Three Amino Acids in the Solid and the Solution Phases
inferred← citeshttps://doi.org/10.21203/rs.3.rs-25677/v3openalex-snapshot
The Binding Behaviors between Cyclopentanocucurbit[6]uril and Three Amino Acids in the Solid and the Solution Phases
inferred← citeshttps://doi.org/10.3390/12040716openalex-snapshot
Synthesis and X-ray Structure of the Inclusion Complex of Dodecamethylcucurbit[6]uril with 1,4-Dihydroxybenzene
inferred← citeshttps://doi.org/10.3390/12071325openalex-snapshot
Chlorine Anion Encapsulation by Molecular Capsules Based on Cucurbit[5]uril and Decamethylcucurbit[5]uril
inferred← citeshttps://doi.org/10.3390/80100074openalex-snapshot
A Method for Synthesizing Partially Substituted Cucurbit[n]uril
inferred← citeshttps://doi.org/10.3390/molecules13112814openalex-snapshot
Structure of Supramolecular Assemblies Formed by α,δ-Tetramethylcucurbit[6]uril and 4-Nitrophenol
inferred← citeshttps://doi.org/10.3390/molecules25040957openalex-snapshot
Probing Reversible Guest Binding with Hyperpolarized 129Xe-NMR: Characteristics and Applications for Cucurbit[n]urils
inferred← citeshttps://doi.org/10.3390/molecules25204627openalex-snapshot
Molecular Sensing with Host Systems for Hyperpolarized 129Xe
inferred← citeshttps://doi.org/10.3762/bjoc.17.194openalex-snapshot
Host–guest interaction and properties of cucurbit[8]uril with chloramphenicol
inferred← citeshttps://doi.org/10.3762/bjoc.6.32openalex-snapshot
Molecular recognition of organic ammonium ions in solution using synthetic receptors
inferred← citeshttps://doi.org/10.3987/com-22-14771openalex-snapshot
Supramolecular Self-Assembly Based on Symmetric Tetramethyl-Substituted Cucurbit[6]uril and Small Aromatic Amines
inferred← citeshttps://doi.org/10.70675/df130d6bzf182z45e3zab34z746fb6b378fcopenalex-snapshot
Functionalized-Cucurbit[n]urils : advanced drug carriers
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