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Methods for Selective Modifications of Cyclodextrins

https://doi.org/10.1021/cr970012b
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Ein Chymotrypsin‐Modell
inferredcites →https://doi.org/10.1002/ange.19911030121openalex-snapshot
Selektive Halogenierung von Cyclomaltooligosacchariden in C6‐Position und Synthese von Per(3,6‐anhydro)cyclomaltooligosacchariden
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Synthese eines lipophilen Cyclodextrin‐[2]‐Rotaxans
inferredcites →https://doi.org/10.1002/ange.19921041029openalex-snapshot
Synthese und Komplexierungsverhalten eines auf Cyclodextrin beruhenden Siderophors
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Synthesis and Characterization of Per‐3,6‐anhydro Cyclodextrins
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Antenna Effect in Multichromophoric Cyclodextrins
inferredcites →https://doi.org/10.1002/anie.199516211openalex-snapshot
β‐Cycloaltrin: A Cyclooligosaccharide Consisting of Seven α(1 → 4)‐Linked Altropyranoses
inferredcites →https://doi.org/10.1002/anie.199718991openalex-snapshot
Synthesis, Structure, and Conformational Features of α‐Cycloaltrin: A Cycloeligosaccharide with Alternating 4C1/1C4 Pyranoid Chairs
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Über Einschlußverbindungen, XX. ORD‐Spektren und Konformation der Glucose‐Einheiten in Cyclodextrinen
inferredcites →https://doi.org/10.1002/cber.19701030718openalex-snapshot
Über Einschlußverbindungen, XXII. Cyclodextrin‐Imidazol‐Verbindungen
inferredcites →https://doi.org/10.1002/cber.19961290902openalex-snapshot
Second‐Sphere Coordination
inferredcites →https://doi.org/10.1002/hlca.19780610622openalex-snapshot
Cyclodextrin chemistry. Selective modification of all primary hydroxyl groups of α‐ and β‐cyclodextrins
inferredcites →https://doi.org/10.1002/ijch.199200004openalex-snapshot
Bifunctional Binding and Catalysis in Host‐Guest Chemistry
inferredcites →https://doi.org/10.1002/jhrc.1240140803openalex-snapshot
Enantiomer separation by gas chromatography on cyclodextrin chiral stationary phases
inferredcites →https://doi.org/10.1002/jhrc.1240140804openalex-snapshot
Gas chromatographic enantiomer separation of agrochemicals using modified cyclodextrins
inferredcites →https://doi.org/10.1002/jlac.19355180107openalex-snapshot
Über Schardingers Dextrine aus Stärke
inferredcites →https://doi.org/10.1002/jlac.19475580102openalex-snapshot
Über Schardingers Dextrine aus Stärke
inferredcites →https://doi.org/10.1002/jlac.1995199506134openalex-snapshot
Molecular modeling of saccharides, 6. Small‐ring cyclodextrins: Their geometries and hydrophobic topographies
inferredcites →https://doi.org/10.1002/jlac.199619960105openalex-snapshot
Molecular Modelling of Saccharides, 9!! On the Hydrophobic Characteristics of Cyclodextrins: Computer‐Aided Visualization of Molecular Lipophilicity Patterns
inferredcites →https://doi.org/10.1002/star.19740260403openalex-snapshot
An Improved Synthesis of 6‐Deoxy‐Analogues of Cyclodextrins and Amylose. Further Interpretations of the Proton Magnetic Resonance Spectra of the Peracetates of Cyclodextrins and Amylose
inferredcites →https://doi.org/10.1002/star.19800320506openalex-snapshot
Synthesis and 13C‐NMR Spectroscopy of Methylated beta‐Cyclodextrins
inferredcites →https://doi.org/10.1002/star.19900421109openalex-snapshot
Halogen Azide Displacement to Prepare Some Symmetrically Substituted β‐Cyclodextrin Derivatives
inferredcites →https://doi.org/10.1002/star.19960480405openalex-snapshot
Towards Understanding Formation and Stability of Cyclodextrin Inclusion Complexes: Computation and Visualization of their Molecular Lipophilicity Patterns[1]
inferredcites →https://doi.org/10.1002/star.19960480606openalex-snapshot
Per‐O‐methylated α‐ and β‐CD: Cyclodextrins with Inverse Hydrophobicity
inferredcites →https://doi.org/10.1007/978-94-015-7797-7openalex-snapshot
Cyclodextrin Technology
inferredcites →https://doi.org/10.1007/bf00656409openalex-snapshot
Catalytic activity of ?-cyclodextrin-histamine
inferredcites →https://doi.org/10.1007/bf00707996openalex-snapshot
Asymmetric reactions with cyclodextrins
inferredcites →https://doi.org/10.1007/bf01041526openalex-snapshot
The lipophilicity patterns of cyclodextrins and of non-glucose cyclooligosaccharides
inferredcites →https://doi.org/10.1007/bf01041532openalex-snapshot
Three-dimensional cyclodextrin: A new class of hosts by trehalose capping of ?-cyclodextrin
inferredcites →https://doi.org/10.1007/bf01041535openalex-snapshot
New type of bridged monoamino-?-Cyclodextrins
inferredcites →https://doi.org/10.1007/bf01053857openalex-snapshot
Conformational mobility in chemically-modified cyclodextrins
inferredcites →https://doi.org/10.1016/0008-6215(88)84140-5openalex-snapshot
Synthesis of 6-O-α-d-glucopyranosylcyclomaltoheptaose
inferredcites →https://doi.org/10.1016/0008-6215(89)80004-7openalex-snapshot
Selective chemical modification of cyclomalto-oligosaccharides via tert-butyldimethylsilylation
inferredcites →https://doi.org/10.1016/0008-6215(89)85176-6openalex-snapshot
Alkylation of cyclomalto-oligosaccharides (cyclodextrins) with dialkyl sulfate-barium hydroxide: Heterogeneity of products and the marked effect of the size of the macrocycle
inferredcites →https://doi.org/10.1016/0008-6215(89)85177-8openalex-snapshot
Exciton coupling, intramolecular self-complexation, and host-guest complex formation of 6A,6X-bis-(anthracene-9-carbonyl) derivatives of cyclomalto-octaose
inferredcites →https://doi.org/10.1016/0008-6215(89)85197-3openalex-snapshot
Synthesis of heptakis(6-O-tert-butyldimethylsilyl)cyclomaltoheptaose and octakis(6-O-tert-butyldimethylsilyl)cyclomalto-octaose
inferredcites →https://doi.org/10.1016/0008-6215(90)84208-copenalex-snapshot
Distribution of substituents in 2-hydroxypropyl ethers of cyclomaltoheptaose
inferredcites →https://doi.org/10.1016/0008-6215(92)80001-hopenalex-snapshot
Preparation of di-O-triphenylmethyl-(trityl)-cyclomalto-hexaoses and -cyclomaltoheptaoses and characterization of three positional isomers of each by the “hex-5-enose degradation”
inferredcites →https://doi.org/10.1016/0008-6215(92)80026-wopenalex-snapshot
Multiple tritylation: a convenient route to polysubstituted derivatives of cyclomaltohexaose
inferredcites →https://doi.org/10.1016/0008-6215(92)80083-dopenalex-snapshot
Synthesis of a cycloheptaose consisting of (1 → 4)-linked 7-amino-6,7-dideoxy-α-d-gluco-heptopyranosyl units: A new analog of cyclomaltoheptaose
inferredcites →https://doi.org/10.1016/0008-6215(92)84039-uopenalex-snapshot
Regioselectivity of the insertion reactions of some aromatic diazo compound complexes with cyclomaltoheptaose
inferredcites →https://doi.org/10.1016/0008-6215(92)84096-bopenalex-snapshot
Synthesis and conformation of dihistamine derivatives of cyclomaltoheptaose (β-cyclodextrin)
inferredcites →https://doi.org/10.1016/0008-6215(92)84117-bopenalex-snapshot
The use of chlorodimethylthexylsilane for protecting the hydroxyl groups in cyclomaltoheptaose (β-cyclodextrin)
inferredcites →https://doi.org/10.1016/0008-6215(94)00251-aopenalex-snapshot
Regioselectivity of alkylation of cyclomaltoheptaose (β-cyclodextrin) and synthesis of its mono-2-O-methyl, -ethyl, -allyl, and -propyl derivatives
inferredcites →https://doi.org/10.1016/0008-6215(94)84184-5openalex-snapshot
Selective pivaloylation and diphenylacetylation of cyclomalto-oligosaccharides
inferredcites →https://doi.org/10.1016/0021-9673(94)80375-7openalex-snapshot
Enantioselective separations by capillary gas chromatography on derivatized cyclodextrins
inferredcites →https://doi.org/10.1016/0022-1902(79)80460-1openalex-snapshot
Preparation and redox properties of a cyclodextrin based ferredoxin model
inferredcites →https://doi.org/10.1016/0040-4020(95)00608-bopenalex-snapshot
The intramolecular inclusion of aromatic esters within β-cyclodextrin as a function of chain length — a detailed NMR study
inferredcites →https://doi.org/10.1016/0040-4039(91)80609-aopenalex-snapshot
The first selective per-tosylation of the secondary OH-2 of β-cyclodextrin
inferredcites →https://doi.org/10.1016/0040-4039(91)85081-fopenalex-snapshot
Formation of amphiphilic cyclodextrins via hydrophobic esterification at the secondary hydroxyl face
inferredcites →https://doi.org/10.1016/0040-4039(94)85003-8openalex-snapshot
Facile preparation of the β-cyclodextrinyl aldehyde
inferredcites →https://doi.org/10.1016/0040-4039(94)88080-8openalex-snapshot
First selective synthesis of thio-β-cyclodextrin derivatives by a direct mitsunobu reaction on free β-cyclodextrin
inferredcites →https://doi.org/10.1016/0040-4039(94)88343-2openalex-snapshot
Synthesis and binding properties of novel cyclodextrin dimers
inferredcites →https://doi.org/10.1016/0040-4039(94)88436-6openalex-snapshot
Per-6-bromo-per-2,3-dimethyl-β-cyclodextrin
inferredcites →https://doi.org/10.1016/0040-4039(95)01808-uopenalex-snapshot
A one-step synthesis of cyclodextrin monoaldehydes
inferredcites →https://doi.org/10.1016/0040-4039(96)00770-8openalex-snapshot
One step synthesis of new urea-linked β-cyclodextrin dimers
inferredcites →https://doi.org/10.1016/0040-4039(96)00916-1openalex-snapshot
Efficient perfacial derivatization of cyclodextrins at the primary face
inferredcites →https://doi.org/10.1016/0040-4039(96)01717-0openalex-snapshot
Bifunctional β-cyclodextrins with two imidazolyl groups specifically attached to C3 positions
inferredcites →https://doi.org/10.1016/0040-4039(96)01944-2openalex-snapshot
Selective modification at the 3-position of β-cyclodextrin
inferredcites →https://doi.org/10.1016/0045-2068(75)90034-6openalex-snapshot
Ester hydrolyses catalyzed by modified cyclodextrins
inferredcites →https://doi.org/10.1016/0045-2068(76)90007-9openalex-snapshot
“Induced-fit”-type complex formation of the model enzyme α-cyclodextrin
inferredcites →https://doi.org/10.1016/0045-2068(76)90018-3openalex-snapshot
Selective alkylation of cycloheptaamylose
inferredcites →https://doi.org/10.1016/0141-3910(96)00029-8openalex-snapshot
On the biostability of a novel β-cyclodextrin based hydrophilic polyurethane
inferredcites →https://doi.org/10.1016/0304-5102(94)00046-8openalex-snapshot
Bifunctional acid—base catalysis by imidazole groups in enzyme mimics
inferredcites →https://doi.org/10.1016/0968-5677(96)00016-8openalex-snapshot
Review: fluorescent cyclodextrins for molecule sensing
inferredcites →https://doi.org/10.1016/s0003-2670(00)83579-5openalex-snapshot
Capillary gas chromatographic separation of enantiomers with stable dipentyl-α, β- and γ-cyclodextrin-derivatized stationary phases
inferredcites →https://doi.org/10.1016/s0006-2952(97)00157-3openalex-snapshot
A basic compositional requirement of agents having heparin-like cell-modulating activities
inferredcites →https://doi.org/10.1016/s0008-6215(00)80256-6openalex-snapshot
Synthesis of monosubstituted cyclohexaamyloses
inferredcites →https://doi.org/10.1016/s0008-6215(00)90568-8openalex-snapshot
Improved preparation of hexakis(6-deoxy)cyclomalto-hexaose and heptakis(6-deoxy)cyclomaltoheptaose
inferredcites →https://doi.org/10.1016/s0021-9673(00)94700-9openalex-snapshot
Methylated cyclodextrin-bonded stationary phases for liquid chromatography
inferredcites →https://doi.org/10.1016/s0021-9673(01)80616-6openalex-snapshot
Analysis of cyclodextrin mixtures by gas chromatography of their dimethylsilyl ethers
inferredcites →https://doi.org/10.1016/s0021-9673(01)88372-2openalex-snapshot
Cyclodextrins and their inclusion complexes
inferredcites →https://doi.org/10.1016/s0021-9673(01)97733-7openalex-snapshot
Preparation and retention behaviour of chemically bonded methylated-cyclodextrin stationary phases for liquid chromatography
inferredcites →https://doi.org/10.1016/s0040-4020(01)88551-3openalex-snapshot
Synthesis of chemically modified cyclodextrins
inferredcites →https://doi.org/10.1016/s0040-4020(01)90271-6openalex-snapshot
Excimer formation in inclusion complexes of modified cyclodextrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)60708-6openalex-snapshot
Synthesis and per-functionalization of heptakis(6-O-carboxymethyl-2,3-di-O-methyl)cyclomaltoheptaose
inferredcites →https://doi.org/10.1016/s0040-4039(00)61134-6openalex-snapshot
Selective preparation of hexakis (6-O-arenesulfonyl) -α-cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(00)73332-6openalex-snapshot
The effect of tether length on the affinity of ligands for bis(cyclodextrins)
inferredcites →https://doi.org/10.1016/s0040-4039(00)73628-8openalex-snapshot
Synthesis of a cradle cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(00)78465-6openalex-snapshot
Synthesis and conformational behaviour of novel cyclodextrin hetero-dimers
inferredcites →https://doi.org/10.1016/s0040-4039(00)78537-6openalex-snapshot
Selective protection of the secondary side of β-cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(00)78589-3openalex-snapshot
The cyclodextrin-nicotinamide compound as a dehydrogenase model simulating apoenzyme-coenzyme-substrate ternary complex system
inferredcites →https://doi.org/10.1016/s0040-4039(00)79100-3openalex-snapshot
A complete set of 3A,6X-di-O-sulfonylated α-cyclodextrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)87639-xopenalex-snapshot
Selective sulfonation of a secondary hydroxyl group of β-cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(00)88899-1openalex-snapshot
An approach to vectorisation of pharmacologically active molecules: The covalent binding of leu-enkephalin to a modified β- cyclodextrin.
inferredcites →https://doi.org/10.1016/s0040-4039(00)95718-6openalex-snapshot
Regioselective sulfonation of a secondary hydroxyl group of cyclodextrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)97599-3openalex-snapshot
A convenient method for functionalization of the 2-position of cyclodextrins
inferredcites →https://doi.org/10.1016/s0040-4039(00)97802-xopenalex-snapshot
Modifications of the secondary hydroxyl side of α-cyclodextrin and nmr studies of them
inferredcites →https://doi.org/10.1016/s0040-4039(00)99358-4openalex-snapshot
A novel synthesis of substituted imidazoles, and a reexamination of a purported chymotrypsin model
inferredcites →https://doi.org/10.1016/s0040-4039(01)81377-0openalex-snapshot
Monotosylated α- and β-cyclodextrins prepared in an alkaline aqueous solution
inferredcites →https://doi.org/10.1016/s0040-4039(01)81618-xopenalex-snapshot
6A6B, 6A6C, and 6A6D-ditosylates of β-cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(01)83804-1openalex-snapshot
Specific host-guest energy transfer by use of β-cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(01)91409-1openalex-snapshot
Convenient preparation and effective separation of the C-2 and C-3 tosylates of α-cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(01)93093-xopenalex-snapshot
Specific Bifunctionalization on Cyclodextrin
inferredcites →https://doi.org/10.1016/s0040-4039(97)00145-7openalex-snapshot
A simple synthesis of a highly water soluble symmetrical β-cyclodextrin derivative
inferredcites →https://doi.org/10.1016/s0040-4039(97)00985-4openalex-snapshot
Regiospecifically multifunctional β-cyclodextrins with two or three glucose residues bearing imidazolyl groups at the C3 positions
inferredcites →https://doi.org/10.1016/s0040-4039(97)10019-3openalex-snapshot
An improved synthesis of 6-deoxyhalo cyclodextrins via halomethylenemorpholinium halides Vilsmeier-Haack type reagents
inferredcites →https://doi.org/10.1016/s0960-894x(00)80446-1openalex-snapshot
Hydrogen bonding effects on the reactivity of a preassociating α-nucleophile. the secondary-side βCD hydroxylamine
inferredcites →https://doi.org/10.1016/s0960-894x(01)80241-9openalex-snapshot
Synthesis of new oligosaccharidyl-thio-β-cyclodextrins (CDS): a novel family of potent drug-targetting vectors.
inferredcites →https://doi.org/10.1016/s0960-894x(01)80558-8openalex-snapshot
Synthesis and glutamate antagonist activity of 4-phosphonoalkylquinoline derivatives: A novel class of non-NMDA antagonist
inferredcites →https://doi.org/10.1016/s0960-894x(01)80559-xopenalex-snapshot
Synthesis of β-cyclodextrin oximes
inferredcites →https://doi.org/10.1016/s0968-0896(00)82172-0openalex-snapshot
Synthesis and transacylating reactivity of β-cyclodextrin ethylenediamines
inferredcites →https://doi.org/10.1016/s0968-0896(96)00222-2openalex-snapshot
Synthesis and biological evaluation of 2-amino-2-deoxy- and 6-amino-6-deoxy-cyclomaltoheptaose polysulfates as synergists for angiogenesis inhibition
inferredcites →https://doi.org/10.1021/ac00034a014openalex-snapshot
Host-guest sensors of 6A,6B-, 6A,6C-, 6A,6D-, and 6A,6E-bis(2-naphthylsulfenyl)-.gamma.-cyclodextrins for detecting organic compounds by fluorescence enhancements
inferredcites →https://doi.org/10.1021/ar00051a008openalex-snapshot
Biomimetic Chemistry and Artificial Enzymes: Catalysis by Design
inferredcites →https://doi.org/10.1021/ar00136a004openalex-snapshot
Miniature organic models of enzymes
inferredcites →https://doi.org/10.1021/cr9403704openalex-snapshot
Artificial Enzymes
inferredcites →https://doi.org/10.1021/cr960133wopenalex-snapshot
Synthetic Cyclic Oligosaccharides
inferredcites →https://doi.org/10.1021/cr970011jopenalex-snapshot
Biomimetic Reactions Catalyzed by Cyclodextrins and Their Derivatives
inferredcites →https://doi.org/10.1021/cr970022copenalex-snapshot
Introduction and General Overview of Cyclodextrin Chemistry
inferredcites →https://doi.org/10.1021/cr970049wopenalex-snapshot
Cyclodextrin-Based Catenanes and Rotaxanes
inferredcites →https://doi.org/10.1021/ja00019a027openalex-snapshot
A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species
inferredcites →https://doi.org/10.1021/ja00030a062openalex-snapshot
Preassociating .alpha.-nucleophiles
inferredcites →https://doi.org/10.1021/ja00039a100openalex-snapshot
Self-assembling systems of the amphiphilic cationic per-6-amino-.beta.-cyclodextrin 2,3-di-O-alkyl ethers
inferredcites →https://doi.org/10.1021/ja00042a021openalex-snapshot
Multichromophoric cyclodextrins. 1. Synthesis of O-naphthoyl-.beta.-cyclodextrins and investigation of excimer formation and energy hopping
inferredcites →https://doi.org/10.1021/ja00073a087openalex-snapshot
Enthalpic domination of the chelate effect in cyclodextrin dimers
inferredcites →https://doi.org/10.1021/ja00076a023openalex-snapshot
Calorimetric titration of inclusion complexation with modified .beta.-cyclodextrins. Enthalpy-entropy compensation in host-guest complexation: from ionophore to cyclodextrin and cyclophane
inferredcites →https://doi.org/10.1021/ja00111a035openalex-snapshot
Sugar-Coated Metalated Macrocycles
inferredcites →https://doi.org/10.1021/ja00147a005openalex-snapshot
Preassociating .alpha.-Nucleophiles Based on .beta.-Cyclodextrin. Their Synthesis and Reactivity
inferredcites →https://doi.org/10.1021/ja00166a021openalex-snapshot
Cooperative binding by aggregated mono-6-(alkylamino)-.beta.-cyclodextrins
inferredcites →https://doi.org/10.1021/ja00169a032openalex-snapshot
Artificial transaminases linking pyridoxamine to binding cavities: controlling the geometry
inferredcites →https://doi.org/10.1021/ja00171a022openalex-snapshot
Synthesis and photochemistry of some anthraquinone-substituted .beta.-cyclodextrins
inferredcites →https://doi.org/10.1021/ja00182a046openalex-snapshot
Strong binding of ditopic substrates by a doubly linked occlusive C1 clamshell as distinguished from an aversive C2 loveseat cyclodextrin dimer
inferredcites →https://doi.org/10.1021/ja00203a050openalex-snapshot
Very strong binding of appropriate substrates by cyclodextrin dimers
inferredcites →https://doi.org/10.1021/ja00221a036openalex-snapshot
Association, photodimerization, and induced-fit types of host-guest complexation of anthracene-appended .gamma.-cyclodextrin derivatives
inferredcites →https://doi.org/10.1021/ja00233a046openalex-snapshot
Synthesis and reactivity of cobalt(III) complexes bearing primary- and secondary-side cyclodextrin binding sites. A tale of two CD's
inferredcites →https://doi.org/10.1021/ja00268a040openalex-snapshot
Mimics of transaminase enzymes
inferredcites →https://doi.org/10.1021/ja00268a050openalex-snapshot
Regiospecific sulfonation onto C-3 hydroxyls of .beta.-cyclodextrin. Preparation and enzyme-based structural assignment of 3A,3C and 3A3D disulfonates
inferredcites →https://doi.org/10.1021/ja00275a042openalex-snapshot
6-Polysubstituted .alpha.-cyclodextrins. Application of Korner's absolute method of isomer determination
inferredcites →https://doi.org/10.1021/ja00297a032openalex-snapshot
Regiospecific sulfonation of secondary hydroxyl groups of .alpha.-cyclodextrin. Its application to preparation of 2A2B, 2A2C-, and 2A2D-disulfonates
inferredcites →https://doi.org/10.1021/ja00330a039openalex-snapshot
Characterization of regiospecific AC- and AD-disulfonate capping of .beta.-cyclodextrin. Capping as an efficient production technique
inferredcites →https://doi.org/10.1021/ja00331a061openalex-snapshot
6A6B-, 6A6C-, and 6A6D-disulfonates of .alpha.-cyclodextrin
inferredcites →https://doi.org/10.1021/ja00343a063openalex-snapshot
Transaminations by pyridoxamine selectively attached at C-3 in .beta.-cyclodextrin
inferredcites →https://doi.org/10.1021/ja00393a056openalex-snapshot
Regiospecific A,C- and A,D-disulfonate capping of .beta.-cyclodextrin
inferredcites →https://doi.org/10.1021/ja00440a083openalex-snapshot
Capped cyclodextrin
inferredcites →https://doi.org/10.1021/ja00449a048openalex-snapshot
Synthesis of cycloheptaamylose 2-, 3-, and 6-phosphoric acids, and a comparative study of their effectiveness as general acid or general base catalysts with bound substrates
inferredcites →https://doi.org/10.1021/ja00463a073openalex-snapshot
Cyclodextrin flexibly capped with metal ion
inferredcites →https://doi.org/10.1021/ja00492a079openalex-snapshot
Very Fast acylation of .beta.-cyclodextrin by bound p-nitrophenyl ferrocinnamate
inferredcites →https://doi.org/10.1021/ja00500a052openalex-snapshot
Duplex cyclodextrin
inferredcites →https://doi.org/10.1021/ja00519a035openalex-snapshot
Symmetrical triamino-per-O-methyl-.alpha.-cyclodextrin: preparation and characterization of primary trisubstituted .alpha.-cyclodextrins
inferredcites →https://doi.org/10.1021/ja00522a054openalex-snapshot
Improved acylation rates within cyclodextrin complexes from flexible capping of the cyclodextrin and from adjustment of the substrate geometry
inferredcites →https://doi.org/10.1021/ja00523a036openalex-snapshot
The first successful carbonic anhydrase model prepared through a new route to regiospecifically bifunctionalized cyclodextrin
inferredcites →https://doi.org/10.1021/ja00526a072openalex-snapshot
Reversing the selectivity of cyclodextrin bisimidazole ribonuclease mimics by changing the catalyst geometry
inferredcites →https://doi.org/10.1021/ja00718a040openalex-snapshot
Detection of a ''Michaelis'' complex by spin labeling in a model enzyme system
inferredcites →https://doi.org/10.1021/ja00848a068openalex-snapshot
Stereochemically correct catalytic site on cyclodextrin resulting in a better enzyme model
inferredcites →https://doi.org/10.1021/ja00989a027openalex-snapshot
Acceleration of phenyl ester cleavage by cycloamyloses. A model for enzymic specificity
inferredcites →https://doi.org/10.1021/ja01091a001openalex-snapshot
The Crystal and Molecular Structure of the Cyclohexaamylose-Potassium Acetate Complex1
inferredcites →https://doi.org/10.1021/ja01167a096openalex-snapshot
Studies on the Schardinger Dextrins. VI. The Molecular Size and Structure of the γ-Dextrin1
inferredcites →https://doi.org/10.1021/ja953061jopenalex-snapshot
Inside−Outside Isomerism of β-Cyclodextrin Covalently Linked with a Naphthyl Group
inferredcites →https://doi.org/10.1021/ja9539812openalex-snapshot
Controlled Orientation of Cyclodextrin Derivatives Immobilized on Gold Surfaces
inferredcites →https://doi.org/10.1021/ja954332topenalex-snapshot
Multichromophoric Cyclodextrins. 4. Light Conversion by Antenna Effect
inferredcites →https://doi.org/10.1021/jf00098a010openalex-snapshot
Relevance of enantiomeric separations in food and beverage analyses
inferredcites →https://doi.org/10.1021/jm00063a018openalex-snapshot
A new candidate for an anti-HIV-1 agent: modified cyclodextrin sulfate (mCDS71)
inferredcites →https://doi.org/10.1021/jo00026a017openalex-snapshot
Per-3,6-anhydro-.alpha.-cyclodextrin and per-3,6-anhydro-.beta.-cyclodextrin
inferredcites →https://doi.org/10.1021/jo00027a031openalex-snapshot
Artificial redox enzymes. 1. Synthetic strategies
inferredcites →https://doi.org/10.1021/jo00061a035openalex-snapshot
Novel cyclodextrin-oligosiloxane copolymers for use as stationary phases to separate enantiomers in open tubular column supercritical fluid chromatography
inferredcites →https://doi.org/10.1021/jo00070a019openalex-snapshot
New permethyl-substituted .beta.-cyclodextrin polysiloxanes for use as chiral stationary phases in open tubular column chromatography
inferredcites →https://doi.org/10.1021/jo00080a049openalex-snapshot
Dual effect of cyclodextrins on pyrocatechol autoxidation
inferredcites →https://doi.org/10.1021/jo00089a041openalex-snapshot
Synthesis of a Water-Soluble Dicyanoanthracene as a Cap For .beta.-Cyclodextrin
inferredcites →https://doi.org/10.1021/jo00097a015openalex-snapshot
The Synthesis and Characterization of a Pyridine-Linked Cyclodextrin Dimer
inferredcites →https://doi.org/10.1021/jo00103a051openalex-snapshot
Synthesis of 6-Deoxychlorocyclodextrin via Vilsmeier-Haack-Type Complexes
inferredcites →https://doi.org/10.1021/jo00103a056openalex-snapshot
Synthesis and Reactivity of 6-.beta.-Cyclodextrin Monoaldehyde: An Electrophilic Cyclodextrin for the Derivatization of Macromolecules under Mild Conditions
inferredcites →https://doi.org/10.1021/jo00114a030openalex-snapshot
A General Method for the Synthesis of Cyclodextrinyl Aldehydes and Carboxylic Acids
inferredcites →https://doi.org/10.1021/jo00117a049openalex-snapshot
A Novel Approach to the Synthesis of Some Chemically-Modified Cyclodextrins
inferredcites →https://doi.org/10.1021/jo00120a023openalex-snapshot
The Synthesis of Functionalized Cyclodextrins As Scaffolds and Templates for Molecular Diversity, Catalysis, and Inclusion Phenomena
inferredcites →https://doi.org/10.1021/jo00125a045openalex-snapshot
Selective Functionalization and Flexible Coupling of Cyclodextrins at the Secondary Hydroxyl Face
inferredcites →https://doi.org/10.1021/jo00127a040openalex-snapshot
Synthesis and Molecular Recognition Properties of a .beta.-Cyclodextrin Tetramer
inferredcites →https://doi.org/10.1021/jo00170a070openalex-snapshot
Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
inferredcites →https://doi.org/10.1021/jo00215a008openalex-snapshot
Regiospecific A,B capping onto .beta.-cyclodextrin. Characteristic remote substituent effect on carbon-13 NMR chemical shift and specific Taka-amylase hydrolysis
inferredcites →https://doi.org/10.1021/jo00222a042openalex-snapshot
Unsymmetrically disubstituted .beta.-cyclodextrins of 6A,6X-dideoxy-6A-azido-6X-[(mesitylsulfonyl)oxy] derivatives
inferredcites →https://doi.org/10.1021/jo00244a018openalex-snapshot
Synthesis of 6A,6X-di-O-(p-tosyl)-.gamma.-cyclodextrins and their structural determination through enzymic hydrolysis of 3A,6A;3X,6X-dianhydro-.gamma.-cyclodextrins
inferredcites →https://doi.org/10.1021/jo00254a019openalex-snapshot
Complete sets of structurally determined 6A,6X-unsymmetrically disubstituted .beta.-cyclodextrins. 6A-S-phenyl-6X-O-(.beta.-naphthylsulfonyl)-6A-thio-.beta.-cyclodextrins and 6A-S-(tert-butyl)-6X-O-(.beta.-naphthylsulfonyl)-6A-thio-.beta.-cyclodextrins
inferredcites →https://doi.org/10.1021/jo00263a008openalex-snapshot
Preparation and photoreaction of 6A,6B-, 6A,6C-, 6A,6D-, and 6A,6E-bis(anthracene-9-carbonyl)-.gamma.-cyclodextrins. A new method for regulation of product stereochemistry
inferredcites →https://doi.org/10.1021/jo00290a016openalex-snapshot
Specific preparation and structure determination of 3A,3C,3E-tri-O-sulfonyl-.beta.-cyclodextrin
inferredcites →https://doi.org/10.1021/jo00380a026openalex-snapshot
Synthesis of specifically modified maltooligosaccharides by enzymic degradation of cyclodextrin derivatives. Substrate-based investigation of the active site of Taka-amylase
inferredcites →https://doi.org/10.1021/jo951396dopenalex-snapshot
Amino Acid Derivatives of β-Cyclodextrin
inferredcites →https://doi.org/10.1021/jo960199ropenalex-snapshot
Epoxides of the Secondary Side of Cyclodextrins1
inferredcites →https://doi.org/10.1021/jo960425xopenalex-snapshot
NMR Studies of Conformations of N-Dansyl- l -leucine-Appended and N-Dansyl- d -leucine-Appended β-Cyclodextrin as Fluorescent Indicators for Molecular Recognition
inferredcites →https://doi.org/10.1021/jo961625bopenalex-snapshot
Molecular Recognition Study on a Supramolecular System. 10. 1 Inclusion Complexation of Modified β-Cyclodextrins with Amino Acids: Enhanced Enantioselectivity for l / d -Leucine
inferredcites →https://doi.org/10.1021/jo9711549openalex-snapshot
Synthesis of Monofacially Functionalized Cyclodextrins Bearing Amino Pendent Groups
inferredcites →https://doi.org/10.1021/jp951598dopenalex-snapshot
Multichromophoric Cyclodextrins. 3. Investigation of Dynamics of Energy Hopping by Frequency-Domain Fluorometry
inferredcites →https://doi.org/10.1021/jp9520308openalex-snapshot
Facile Dimerization of Viologen Radical Cations Covalently Bonded to β-Cyclodextrin and Suppression of the Dimerization by β-Cyclodextrin and Amphiphiles
inferredcites →https://doi.org/10.1021/js950534bopenalex-snapshot
Pharmaceutical Applications of Cyclodextrins. 1. Drug Solubilization and Stabilization
inferredcites →https://doi.org/10.1021/la960144kopenalex-snapshot
Comparison of Host−Guest Langmuir−Blodgett Multilayer Formation by Two Different Amphiphilic Cyclodextrins
inferredcites →https://doi.org/10.1023/a:1015907927950openalex-snapshot
Amorphous Water-Soluble Cyclodextrin Derivatives: 2-Hydroxyethyl, 3-Hydroxypropyl, 2-Hydroxyisobutyl, and Carboxamidomethyl Derivatives of β-Cyclodextrin
inferredcites →https://doi.org/10.1023/a:1018926508695openalex-snapshot
Preparation of Heptakis(2,6-di-O-ethyl)-β-cyclodextrin and Its Nuclear Magnetic Resonance Spectroscopic Characterization
inferredcites →https://doi.org/10.1038/371320a0openalex-snapshot
Photochemical closing and opening of the guest-binding cavity of cyclodextrins
inferredcites →https://doi.org/10.1039/a606245hopenalex-snapshot
Photo-responsive catalysis by thymine–cyclodextrin conjugates
inferredcites →https://doi.org/10.1039/a701905jopenalex-snapshot
Discrimination between deoxycholic acid epimers by fluorescence of excimer-forming 6A,6E-O-bis[2-(1-naphthyl)propanoyl]- γ-cyclodextrins
inferredcites →https://doi.org/10.1039/a703575fopenalex-snapshot
A cyclodextrin to reverse the regioselectivity of nitrile oxide cycloaddition to a terminal alkene
inferredcites →https://doi.org/10.1039/c39840001277openalex-snapshot
Fully collaborative guest binding by a double cyclodextrin host
inferredcites →https://doi.org/10.1039/c39850001001openalex-snapshot
Synthesis of new chiral macrocyclic polyhydroxy ethers by reduction of cyclodextrins
inferredcites →https://doi.org/10.1039/c39900000010openalex-snapshot
Artificial enzymes: synthesis of imidazole substituted at C(2) of β-cyclodextrin as an efficient enzyme model of chymotrypsin
inferredcites →https://doi.org/10.1039/c39910000759openalex-snapshot
Chiral differentiation in the deacylation of 6 A -O-{2-[4-(2-methylpropyl)phenyl]propanoyl}-β-cyclodextrin
inferredcites →https://doi.org/10.1039/c39920000153openalex-snapshot
A chiral sensor based on a peroctylated α-cyclodextrin
inferredcites →https://doi.org/10.1039/c39920001112openalex-snapshot
Heptakis-2,3-epoxy-β-cyclodextrin, a key intermediate in the synthesis of custom designed cyclodextrins
inferredcites →https://doi.org/10.1039/c39930000438openalex-snapshot
Cyclodextrin liquid crystals: synthesis and self-organisation of amphiphilic thio-β-cyclodextrins
inferredcites →https://doi.org/10.1039/c39930000636openalex-snapshot
Preparation of octakis(3,6-anhydro)-γ-cyclodextrin and characterization of its cation binding ability
inferredcites →https://doi.org/10.1039/c39930000691openalex-snapshot
Selective binding and detection of onium ions by lipophilic neutral cyclodextrins
inferredcites →https://doi.org/10.1039/c39950000581openalex-snapshot
Synthesis of a ‘head-to-tail’ type cyclodextrin dimer linked by a disulfide bridge
showing the first 200 of 246 · page through all 246

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Adamantane-containing drug delivery systems
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Solid State and Solution Conformation of 6-[4-[N-tert-ButoxycarbonylN-(N′-ethyl)propanamide]imidazolyl]-6-deoxycyclomaltoheptaose: Evidence of Self-Inclusion of the Boc Group within the β-Cyclodextrin Cavity
inferred← citeshttps://doi.org/10.1002/0471264180.os077.24openalex-snapshot
6 A ‐O‐p‐Toluenesulfonyl‐β‐Cyclodextrin
inferred← citeshttps://doi.org/10.1002/0471440264.pst649openalex-snapshot
Pillar[ n ]arenes: Synthesis, Structure, and Applications
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Metal Assembly of Cyclodextrin Recognition Sites
inferred← citeshttps://doi.org/10.1002/1099-1395(200101)14:1<11::aid-poc329>3.0.co;2-7openalex-snapshot
Inclusion complexation of ?-cyclodextrin and 6-O-?-�maltosyl- and 2-O-(2-hydroxypropyl)-?-cyclodextrins �with some fluorescent dyes
inferred← citeshttps://doi.org/10.1002/1521-3757(20001016)112:20<3756::aid-ange3756>3.0.co;2-uopenalex-snapshot
Diisobutylaluminum-Promoted Regioselective De-O-benzylation of Perbenzylated Cyclodextrins: A Powerful New Strategy for the Preparation of Selectively Modified Cyclodextrins
inferred← citeshttps://doi.org/10.1002/1521-3773(20001016)39:20<3610::aid-anie3610>3.0.co;2-vopenalex-snapshot
Diisobutylaluminum-Promoted Regioselective De-O-benzylation of Perbenzylated Cyclodextrins: A Powerful New Strategy for the Preparation of Selectively Modified Cyclodextrins
inferred← citeshttps://doi.org/10.1002/1522-2683(200101)22:1<109::aid-elps109>3.0.co;2-popenalex-snapshot
Evaluation of norbornene- β-cyclodextrin-based monomers and oligomers as chiral selectors by means of nonaqueous capillary electrophoresis
inferred← citeshttps://doi.org/10.1002/1522-2683(200109)22:15<3171::aid-elps3171>3.0.co;2-kopenalex-snapshot
Enantiomeric separation of hydroxy acids and carboxylic acids by diamino-β-cyclodextrins (AB, AC, AD) in capillary electrophoresis
inferred← citeshttps://doi.org/10.1002/1615-9314(20020901)25:13<789::aid-jssc789>3.0.co;2-jopenalex-snapshot
Synthesis and applications of adsorbents containing cyclodextrins
inferred← citeshttps://doi.org/10.1002/9780470583463.ch3openalex-snapshot
Molecular Encapsulation of Redox‐Active Guests
inferred← citeshttps://doi.org/10.1002/9780470661345.smc055openalex-snapshot
Cyclodextrins: From Nature to Nanotechnology
inferred← citeshttps://doi.org/10.1002/9780470669143.ch8openalex-snapshot
Fluorescence Studies of the Hydrogen Bonding of Excited‐State Molecules within Supramolecular Host–Guest Inclusion Complexes
inferred← citeshttps://doi.org/10.1002/9780470926819.ch11openalex-snapshot
Amphiphilic Cyclodextrins: Synthesis and Characterization
inferred← citeshttps://doi.org/10.1002/9780470926819.ch14openalex-snapshot
Cyclodextrins and Biotechnological Applications
inferred← citeshttps://doi.org/10.1002/9781118867334.ch11openalex-snapshot
Chirality in Organic Hosts
inferred← citeshttps://doi.org/10.1002/9781118887813.ch1openalex-snapshot
A Supramolecular Approach to Macromolecular Self&;#x02010;Assembly: Cyclodextrin Host/Guest Complexes
inferred← citeshttps://doi.org/10.1002/9781119044123.ch2openalex-snapshot
The Fundamentals of Making Mechanical Bonds
inferred← citeshttps://doi.org/10.1002/9781119247609.ch2openalex-snapshot
Supramolecular Chemistry and Rotaxane
inferred← citeshttps://doi.org/10.1002/9783527613502.ch10openalex-snapshot
Combinatorial Approaches to Molecular Receptors for Chemosensors
inferred← citeshttps://doi.org/10.1002/9783527639786.ch2openalex-snapshot
Cyclodextrin‐Based Supramolecular Polymers
inferred← citeshttps://doi.org/10.1002/9783527639786.ch5openalex-snapshot
Polymers Containing Covalently Bonded and Supramolecularly Attached Cyclodextrins as Side Groups
inferred← citeshttps://doi.org/10.1002/9783527656790.ch4openalex-snapshot
Water‐Soluble Hydroformylation Catalysis
inferred← citeshttps://doi.org/10.1002/9783527656875.ch2openalex-snapshot
Metallic Nanoparticles in Neat Water for Catalytic Applications
inferred← citeshttps://doi.org/10.1002/9783527658947.ch9openalex-snapshot
Advances in Cyclodextrin Chemistry
inferred← citeshttps://doi.org/10.1002/9783527697014.ch13openalex-snapshot
Cyclodextrin Chemistry via Selective Protecting Group Manipulations
inferred← citeshttps://doi.org/10.1002/9783527804948.ch4openalex-snapshot
Cyclic Host Liquids for the Formation of Rotaxanes and Their Applications
inferred← citeshttps://doi.org/10.1002/adfm.201201847openalex-snapshot
Carbonyl‐β‐Cyclodextrin as a Novel Binder for Sulfur Composite Cathodes in Rechargeable Lithium Batteries
inferred← citeshttps://doi.org/10.1002/adfm.201201902openalex-snapshot
Modular Multifunctional Poly(ethylene glycol) Hydrogels for Stem Cell Differentiation
inferred← citeshttps://doi.org/10.1002/adfm.201504048openalex-snapshot
A Supramolecule‐Triggered Mechanochromic Switch of Cyclodextrin‐Jacketed Rhodamine and Spiropyran Derivatives
inferred← citeshttps://doi.org/10.1002/adfm.201909049openalex-snapshot
Recent Advances in Host–Guest Self‐Assembled Cyclodextrin Carriers: Implications for Responsive Drug Delivery and Biomedical Engineering
inferred← citeshttps://doi.org/10.1002/adma.200600812openalex-snapshot
Cationic Supramolecules Composed of Multiple Oligoethylenimine‐Grafted β‐Cyclodextrins Threaded on a Polymer Chain for Efficient Gene Delivery
inferred← citeshttps://doi.org/10.1002/adma.201606641openalex-snapshot
Cyclodextrin Films with Fast Solvent Transport and Shape‐Selective Permeability
inferred← citeshttps://doi.org/10.1002/adma.202404164openalex-snapshot
Unraveling Anomalies in Preferential Liquid Transport through the Intrinsic Pores of Cyclodextrin in Polyester Nanofilms
inferred← citeshttps://doi.org/10.1002/adsc.200303149openalex-snapshot
Cyclodextrins or Calixarenes: What is the Best Mass Transfer Promoter for Suzuki Cross‐Coupling Reactions in Water?
inferred← citeshttps://doi.org/10.1002/ange.200462678openalex-snapshot
Synthesis of a Cycloallin Derivative from β‐Cyclodextrin: Heptakis(2,3‐dideoxy‐2,3‐epithio)‐β‐cycloallin
inferred← citeshttps://doi.org/10.1002/ange.200500509openalex-snapshot
Modifizierte lineare Dextrine (“Acyclodextrine”) als chirale Selektoren zur gaschromatographischen Trennung von Enantiomeren
inferred← citeshttps://doi.org/10.1002/ange.200701156openalex-snapshot
Imidazolyl Cyclodextrins: Artificial Serine Proteases Enabling Regiospecific Reactions
inferred← citeshttps://doi.org/10.1002/ange.200802947openalex-snapshot
Bindungsmechanismen in supramolekularen Komplexen
inferred← citeshttps://doi.org/10.1002/ange.200901200openalex-snapshot
Self‐Mediated Stereoselective Oxidation of Thia‐Capped Cyclodextrins
inferred← citeshttps://doi.org/10.1002/ange.201105737openalex-snapshot
Diisobutylaluminum Hydride Mediated Regioselective O Desilylations: Access to Multisubstituted Cyclodextrins
inferred← citeshttps://doi.org/10.1002/ange.201402917openalex-snapshot
Cyclodextrin‐Templated Porphyrin Nanorings
inferred← citeshttps://doi.org/10.1002/ange.201612150openalex-snapshot
Dynamisches makromolekulares Materialdesign – die Vielseitigkeit von Cyclodextrin‐basierter Wirt‐Gast‐Chemie
inferred← citeshttps://doi.org/10.1002/ange.202011348openalex-snapshot
Synthesis of Single Isomeric Complexes with Dissymmetric Structures Using Macrocyclic Homooligomers
inferred← citeshttps://doi.org/10.1002/ange.202102182openalex-snapshot
Programmed Synthesis of Hepta‐Differentiated β‐Cyclodextrin: 1 out of 117655 Arrangements
inferred← citeshttps://doi.org/10.1002/ange.202501058openalex-snapshot
Cyclodextrin‐Initiated N‐Carboxyanhydride Polymerization for the Design of Stereostructural Dobby Polypeptides with Jellyfish‐Type Architecture
inferred← citeshttps://doi.org/10.1002/ange.4608575openalex-snapshot
Host–Guest Mismatch Enables Selective Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/anie.200462678openalex-snapshot
Synthesis of a Cycloallin Derivative from β‐Cyclodextrin: Heptakis(2,3‐dideoxy‐2,3‐epithio)‐β‐cycloallin
inferred← citeshttps://doi.org/10.1002/anie.200500509openalex-snapshot
Modified Linear Dextrins (“Acyclodextrins”) as New Chiral Selectors for the Gas‐Chromatographic Separation of Enantiomers
inferred← citeshttps://doi.org/10.1002/anie.200701156openalex-snapshot
Imidazolyl Cyclodextrins: Artificial Serine Proteases Enabling Regiospecific Reactions
inferred← citeshttps://doi.org/10.1002/anie.200802947openalex-snapshot
Binding Mechanisms in Supramolecular Complexes
inferred← citeshttps://doi.org/10.1002/anie.200901200openalex-snapshot
Self‐Mediated Stereoselective Oxidation of Thia‐Capped Cyclodextrins
inferred← citeshttps://doi.org/10.1002/anie.201105737openalex-snapshot
Diisobutylaluminum Hydride Mediated Regioselective O Desilylations: Access to Multisubstituted Cyclodextrins
inferred← citeshttps://doi.org/10.1002/anie.201402917openalex-snapshot
Cyclodextrin‐Templated Porphyrin Nanorings
inferred← citeshttps://doi.org/10.1002/anie.201612150openalex-snapshot
Dynamic Macromolecular Material Design—The Versatility of Cyclodextrin‐Based Host–Guest Chemistry
inferred← citeshttps://doi.org/10.1002/anie.202011348openalex-snapshot
Synthesis of Single Isomeric Complexes with Dissymmetric Structures Using Macrocyclic Homooligomers
inferred← citeshttps://doi.org/10.1002/anie.202102182openalex-snapshot
Programmed Synthesis of Hepta‐Differentiated β‐Cyclodextrin: 1 out of 117655 Arrangements
inferred← citeshttps://doi.org/10.1002/anie.202501058openalex-snapshot
Cyclodextrin‐Initiated N‐Carboxyanhydride Polymerization for the Design of Stereostructural Dobby Polypeptides with Jellyfish‐Type Architecture
inferred← citeshttps://doi.org/10.1002/anie.4608575openalex-snapshot
Host–Guest Mismatch Enables Selective Hydrogen Atom Transfer
inferred← citeshttps://doi.org/10.1002/aoc.5862openalex-snapshot
Design, preparation, and characterization of Fe3O4 nanoparticles encapsulating β‐cyclodextrin‐bearing guanidine as a highly efficient and reusable heterogeneous base catalyst for synthesis of 3,4‐dihydropyrano[3,2‐c]chromenes
inferred← citeshttps://doi.org/10.1002/aoc.6378openalex-snapshot
Nickel/β‐CD‐catalyzed Suzuki–Miyaura cross‐coupling of aryl boronic acids with aryl halides in water
inferred← citeshttps://doi.org/10.1002/aoc.7287openalex-snapshot
Recent advances in β‐cyclodextrin‐based catalysts for reducing toxic nitroaromatic: An overview
inferred← citeshttps://doi.org/10.1002/aoc.7365openalex-snapshot
The recent development of β‐cyclodextrin‐based catalysts system in click reactions: A review
inferred← citeshttps://doi.org/10.1002/aoc.7458openalex-snapshot
The recent development of β‐cyclodextrin‐based catalysts system in Suzuki coupling reactions
inferred← citeshttps://doi.org/10.1002/app.21829openalex-snapshot
Methacryloylpropyl–βcyclodextrin and vinylpyrrolidone copolymers: Synthesis and characterization as potential chiral selector
inferred← citeshttps://doi.org/10.1002/app.29657openalex-snapshot
Synthesis and characterization of a novel liquid crystalline star‐shaped polymer based on α‐CD core via ATRP
inferred← citeshttps://doi.org/10.1002/app.34630openalex-snapshot
Synthesis, characterization, and degradation investigation of water‐soluble β‐cyclodextrin‐based epoxy resins
inferred← citeshttps://doi.org/10.1002/app.38127openalex-snapshot
Synthesis of sulfated β‐cyclodextrin/cotton/ZnO nano composite for improve the antibacterial activity and dyeability with Azadirachta indica
inferred← citeshttps://doi.org/10.1002/app.47632openalex-snapshot
Photo‐grafting of β‐cyclodextrin onto the polyethersulfone microfiltration‐membrane: Fast surface hydrophilicity improvement and continuous phthalate ester removal
inferred← citeshttps://doi.org/10.1002/app.51524openalex-snapshot
Synthesis and performance of a novel polycarboxylate superplasticizer through grafting the β‐cyclodextrin on the side chain by click reaction
inferred← citeshttps://doi.org/10.1002/asia.202500876openalex-snapshot
Nanosponges for Chemosensors and Biosensors: Next Generation Functional Materials
inferred← citeshttps://doi.org/10.1002/bip.22290openalex-snapshot
Amphiphilic Cytosolic Glycans from Mycobacteria: Occurrence, Lipid‐Binding Properties, Biosynthesis, and Synthesis
inferred← citeshttps://doi.org/10.1002/cctc.201200718openalex-snapshot
Methylated β‐Cyclodextrin‐Capped Ruthenium Nanoparticles: Synthesis Strategies, Characterization, and Application in Hydrogenation Reactions
inferred← citeshttps://doi.org/10.1002/ceur.202500473openalex-snapshot
Cyclodextrin‐Amino Acid Conjugates: Synthesis and Pharmaceutical Applications
inferred← citeshttps://doi.org/10.1002/chem.200500364openalex-snapshot
Artificial Glycosyl Phosphorylases
inferred← citeshttps://doi.org/10.1002/chem.200501187openalex-snapshot
Synthesis of Bridged and Metallobridged Bis(β‐cyclodextrin)s Containing Fluorescent Oxamidobisbenzoyl Linkers and Their Selective Binding towards Bile Salts
inferred← citeshttps://doi.org/10.1002/chem.200501548openalex-snapshot
Photoinduced Electron Transfer in α‐Cyclodextrin‐Based Supramolecular Dyads: A Free‐Energy‐Dependence Study
inferred← citeshttps://doi.org/10.1002/chem.200601756openalex-snapshot
An Anthracene‐Appended β‐Cyclodextrin‐Based Dyad: Study of Self‐Assembly and Photoinduced Electron‐Transfer Processes
inferred← citeshttps://doi.org/10.1002/chem.200701650openalex-snapshot
Synthesis, Characterization, and Remarkable Biological Properties of Cyclodextrins Bearing Guanidinoalkylamino and Aminoalkylamino Groups on Their Primary Side
inferred← citeshttps://doi.org/10.1002/chem.200701770openalex-snapshot
Highly Selective Synthesis of a 1,3,5‐Tris‐Protected Calix[6]arene‐Type Molecular Platform through Coordination and Host–Guest Chemistry
inferred← citeshttps://doi.org/10.1002/chem.201002541openalex-snapshot
Regioselective Double Capping of Cyclodextrin Scaffolds
inferred← citeshttps://doi.org/10.1002/chem.201102266openalex-snapshot
The Multivalent Effect in Glycosidase Inhibition: Probing the Influence of Architectural Parameters with Cyclodextrin‐based Iminosugar Click Clusters
inferred← citeshttps://doi.org/10.1002/chem.201202391openalex-snapshot
Guest Covalent Capture by a Host: A Biomimetic Strategy for the Selective Functionalization of a Cavity
inferred← citeshttps://doi.org/10.1002/chem.201503131openalex-snapshot
Access to Versatile β‐Cyclodextrin Scaffolds through Guest‐Mediated Monoacylation
inferred← citeshttps://doi.org/10.1002/chem.201700782openalex-snapshot
Secondary‐Rim γ‐Cyclodextrin Functionalization to Conjugate with C60: Improved Efficacy as a Photosensitizer
inferred← citeshttps://doi.org/10.1002/chem.201705647openalex-snapshot
Mechanochemical Preparation of Stable Sub‐100 nm γ‐Cyclodextrin:Buckminsterfullerene (C60) Nanoparticles by Electrostatic or Steric Stabilization
inferred← citeshttps://doi.org/10.1002/chem.201806090openalex-snapshot
Direct and Regioselective Di‐α‐fucosylation on the Secondary Rim of β‐Cyclodextrin
inferred← citeshttps://doi.org/10.1002/chem.201903945openalex-snapshot
Chemical Modification of β‐Cyclodextrins: Balancing Soft and Rigid Domains in Complex Structures
inferred← citeshttps://doi.org/10.1002/chem.71603openalex-snapshot
Targeting Cancer Cells With Self‐Assembled Ru‐Polysaccharide Photocatalyst for Visible‐Light‐Induced Activation of Prodrugs
inferred← citeshttps://doi.org/10.1002/chin.199839319openalex-snapshot
ChemInform Abstract: Methods for Selective Modifications of Cyclodextrins
inferred← citeshttps://doi.org/10.1002/chir.20069openalex-snapshot
New chiral selectors: Design and synthesis of 6‐TBDMS‐2,3‐methyl β‐cyclodextrin 2‐2′ thioureido dimer and 6‐TBDMS‐2,3‐methyl (or 2‐methyl‐3‐acetyl) β‐cyclodextrin bearing an (R) mosher acid moiety
inferred← citeshttps://doi.org/10.1002/chir.20571openalex-snapshot
Molecular dynamics study on the conformational flexibility and energetics in aqueous solution of methylated β‐cyclodextrins
inferred← citeshttps://doi.org/10.1002/cite.202400148openalex-snapshot
Additives in Biphasic Hydroformylation: An Analysis of the Influence of the Interfacial Area
inferred← citeshttps://doi.org/10.1002/cjoc.20020200420openalex-snapshot
Synthesis and Characterization of β‐Cyclodextrin Bonded Metal Porphyrins
inferred← citeshttps://doi.org/10.1002/cjoc.201300270openalex-snapshot
Cyclodextrin‐Based Porous Nanocapsules
inferred← citeshttps://doi.org/10.1002/cmdc.201000419openalex-snapshot
Symmetry Complementarity‐Guided Design of Anthrax Toxin Inhibitors Based on β‐Cyclodextrin: Synthesis and Relative Activities of Face‐Selective Functionalized Polycationic Clusters
inferred← citeshttps://doi.org/10.1002/cplu.201300229openalex-snapshot
Cyclodextrin‐Based Ionic Liquids as Enantioselective Stationary Phases in Gas Chromatography
inferred← citeshttps://doi.org/10.1002/cplu.201800348openalex-snapshot
Effective Guest Inclusion by a 6‐O‐Modified β‐Cyclodextrin Dimer in Organic Solvents
inferred← citeshttps://doi.org/10.1002/cplu.70247openalex-snapshot
Cyclodextrins and Cyclodextrin‐Based Polymers and Their Supramolecular Host–Guest Interactions for Sustainable Water Purification and Perovskite Solar Cell Devices: A Review
inferred← citeshttps://doi.org/10.1002/ejic.201101316openalex-snapshot
Functionalized Cyclodextrins as First and Second Coordination Sphere Ligands for Aqueous Organometallic Catalysis
inferred← citeshttps://doi.org/10.1002/ejoc.200300108openalex-snapshot
Synthesis, NMR Spectroscopic Characterization and Polysiloxane‐Based Immobilization of the Three Regioisomeric Monooctenylpermethyl‐β‐cyclodextrins and Their Application in Enantioselective GC
inferred← citeshttps://doi.org/10.1002/ejoc.200390193openalex-snapshot
Selective Tetrafunctionalisation of α‐Cyclodextrin using the Supertrityl Protecting Group − Synthesis of the First C2‐Symmetric Tetraphosphane Based on a Cavitand (α‐TEPHOS)
inferred← citeshttps://doi.org/10.1002/ejoc.200400162openalex-snapshot
Construction of a Fused Polycyclic Wall within the Cyclodextrin Belt To Ensure a Distorted Cavity: An Unusual trans‐Diequatorial Ring‐Opening Reaction of Cyclodextrin Epoxide Rings
inferred← citeshttps://doi.org/10.1002/ejoc.200500034openalex-snapshot
Artificial Epoxidase II. Synthesis of Cyclodextrin Ketoesters and Epoxidation of Alkenes
inferred← citeshttps://doi.org/10.1002/ejoc.200700933openalex-snapshot
Amphiphilic Cyclodextrins – Advances in Synthesis and Supramolecular Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.200701113openalex-snapshot
External vs. Internal Interactions in the Enantiodiscrimination of Fluorinated α‐Amino Acid Derivatives by Heptakis[2,3‐di‐O‐acetyl‐6‐O‐(tert‐butyldimethylsilyl)]‐β‐cyclodextrin, a Powerful Chiral Solvating Agent for NMR Spectroscopy
inferred← citeshttps://doi.org/10.1002/ejoc.200800930openalex-snapshot
Cap‐Assisted Synthesis of Hetero‐Trifunctional Cyclodextrins, from Flamingo Cap to Bascule Bridge
inferred← citeshttps://doi.org/10.1002/ejoc.200901099openalex-snapshot
Amino–Acetone‐Bridged Cyclodextrins ― Artificial Alcohol Oxidases
inferred← citeshttps://doi.org/10.1002/ejoc.200901230openalex-snapshot
Diisobutylaluminium Hydride (DIBAL‐H) Promoted Secondary Rim Regioselective Demethylations of Permethylated β‐Cyclodextrin: A Mechanistic Proposal
inferred← citeshttps://doi.org/10.1002/ejoc.201000295openalex-snapshot
The Grignard Reaction of Cyclodextrin‐6‐aldehydes Revisited: A Study of the Stereoselectivity Upon Addition of Organometallic Reagents to Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.201200404openalex-snapshot
Synthesis of Cyclodextrins with Carboxylic Acids at the Secondary Rim and an Evaluation of Their Properties as Chemzymes for Glycoside Hydrolysis
inferred← citeshttps://doi.org/10.1002/ejoc.201200756openalex-snapshot
Synthesis of Tin‐Containing Cyclodextrins as Potential Enzyme Models
inferred← citeshttps://doi.org/10.1002/ejoc.201300880openalex-snapshot
Multivalent Functionalization of Cyclodextrins by Photochemical Thiol‐Ene Addition Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201301681openalex-snapshot
Limits of the Inversion Phenomenon in Triazolyl‐Substituted β‐Cyclodextrin Dimers
inferred← citeshttps://doi.org/10.1002/ejoc.201402802openalex-snapshot
Controlled Acid‐Mediated Regioselective O‐Desilylations for Multifunctionalization of Cyclodextrins
inferred← citeshttps://doi.org/10.1002/ejoc.201600693openalex-snapshot
Monosubstituted Cyclodextrins as Precursors for Further Use
inferred← citeshttps://doi.org/10.1002/elps.200390126openalex-snapshot
Comparative enantioseparations with native β‐cyclodextrin, randomly acetylated β‐cyclodextrin and heptakis‐(2,3‐di‐O‐acetyl)‐β‐cyclodextrin in capillary electrophoresis
inferred← citeshttps://doi.org/10.1002/elps.202200178openalex-snapshot
From capillaries to microchips, green electrophoretic features for enantiomeric separations: A decade review (2013–2022)
inferred← citeshttps://doi.org/10.1002/elps.70116openalex-snapshot
Cyclodextrins as Chiral Selectors in Capillary Electrophoresis—Recent Developments in Understanding Analyte Complexation and Applications in Pharmaceutical Analysis
inferred← citeshttps://doi.org/10.1002/ep.12343openalex-snapshot
A new green method for the preparation of titanium dioxide‐graphene composite using cyclodextrin as a linker with enhanced photoexcited electron transfer and photocatalytic properties
inferred← citeshttps://doi.org/10.1002/ffj.2019openalex-snapshot
A review on cyclodextrin encapsulation of essential oils and volatiles
inferred← citeshttps://doi.org/10.1002/hlca.201100026openalex-snapshot
Inclusion Complexes of Coenzyme Q10 with Polyamine‐Modified β‐Cyclodextrins: Characterization, Solubilization, and Inclusion Mode
inferred← citeshttps://doi.org/10.1002/ijch.201100160openalex-snapshot
1,2,3‐Triazolophanes—Cyclophanes with an Array of Molecular Structures and Supramolecular Architectures
inferred← citeshttps://doi.org/10.1002/jbm.a.31976openalex-snapshot
Cationic supramolecules consisting of oligoethylenimine‐grafted α‐cyclodextrins threaded on poly(ethylene oxide) for gene delivery
inferred← citeshttps://doi.org/10.1002/jbm.b.33496openalex-snapshot
Sulfobutyl ether β‐cyclodextrin (Captisol®) and methyl β‐cyclodextrin enhance and stabilize fluorescence of aqueous indocyanine green
inferred← citeshttps://doi.org/10.1002/jctb.1525openalex-snapshot
Thermodynamics of the encapsulation by cyclodextrins
inferred← citeshttps://doi.org/10.1002/jctb.2295openalex-snapshot
A facile and practical approach to randomly methylated β‐cyclodextrin
inferred← citeshttps://doi.org/10.1002/jhet.5570440405openalex-snapshot
New fluorescent bis‐β‐cyclodextrin‐indolizine sensor. Synthesis and sensing ability
inferred← citeshttps://doi.org/10.1002/jps.22352openalex-snapshot
Hydroxypropyl-β-Cyclodextrin Copolymers and Their Nanoparticles as Doxorubicin Delivery System
inferred← citeshttps://doi.org/10.1002/jrs.5372openalex-snapshot
Hydration properties and water structure in aqueous solutions of native and modified cyclodextrins by UV R aman and B rillouin scattering
inferred← citeshttps://doi.org/10.1002/jssc.200700631openalex-snapshot
Single‐step approach to β‐cyclodextrin‐bonded silica as monolithic stationary phases for CEC
inferred← citeshttps://doi.org/10.1002/jssc.200800357openalex-snapshot
Monosubstituted positively charged cyclodextrins: Synthesis and applications in chiral separation
inferred← citeshttps://doi.org/10.1002/mabi.201800281openalex-snapshot
Dynamic Hydrogels from Host–Guest Supramolecular Interactions
inferred← citeshttps://doi.org/10.1002/mabi.202200090openalex-snapshot
Implementation of Water‐Soluble Cyclodextrin‐Based Polymers in Biomedical Applications: How Far Are We?
inferred← citeshttps://doi.org/10.1002/macp.200400192openalex-snapshot
Novel Possibilities by Cationic Ring‐Opening Polymerisation of Cyclodextrin Derivatives: Preparation of a Copolymer Bearing Block‐Like Sequences of Tri‐O‐methylglucosyl Units
inferred← citeshttps://doi.org/10.1002/macp.201600102openalex-snapshot
Chemical Sensors Based on New Polyamides Biobased on (Z) Octadec‐9‐Enedioic Acid and β‐Cyclodextrin
inferred← citeshttps://doi.org/10.1002/macp.202500492openalex-snapshot
Ultra‐High Molecular Weight 21‐Arm Star‐Shaped Polyacrylates via Cu(0)‐RDRP
inferred← citeshttps://doi.org/10.1002/mrc.3917openalex-snapshot
Study of near‐symmetric cyclodextrins by compressed sensing 2D NMR
inferred← citeshttps://doi.org/10.1002/pi.2355openalex-snapshot
Polymerization in magnetic field: XVIII. Influence of surfactant nature on the synthesis and thermal properties of poly(methyl methacrylate) and poly[(methyl methacrylate)‐co‐(epoxypropyl methacrylate)]
inferred← citeshttps://doi.org/10.1002/pola.20837openalex-snapshot
Synthesis of well‐defined AB 20 ‐type star polymers with cyclodextrin‐core by combination of NMP and ATRP
inferred← citeshttps://doi.org/10.1002/pola.22497openalex-snapshot
Poly(4‐acryloylmorpholine) oligomers carrying a β‐cyclodextrin residue at one terminus
inferred← citeshttps://doi.org/10.1002/pola.23610openalex-snapshot
Cyclodextrin polyrotaxanes assembled from a molecular construction kit in aqueous solution
inferred← citeshttps://doi.org/10.1002/pola.23666openalex-snapshot
Assembly of a fluorescent cyclodextrin polyrotaxane and its detection by fluorescence microscopy
inferred← citeshttps://doi.org/10.1002/pola.24921openalex-snapshot
Three different β‐cyclodextrins direct the emulsion copolymerization of a highly fluorinated methacrylate toward distinctive nanostructured particle morphologies
inferred← citeshttps://doi.org/10.1002/prep.201800137openalex-snapshot
Nitrated Cross‐linked β‐Cyclodextrin Binders Exhibiting Low Glass Transition Temperatures
inferred← citeshttps://doi.org/10.1002/rcm.2175openalex-snapshot
Characterization of a new methylated β ‐cyclodextrin with a low degree of substitution by electrospray ionization mass spectrometry and liquid chromatography/mass spectrometry
inferred← citeshttps://doi.org/10.1002/slct.201601630openalex-snapshot
Host‐Guest Chemistry of Linked β‐ and γ‐Cyclodextrin Dimers and 1‐ and 2‐Naphthyl‐Sulfonamide Substituted Poly(acrylate)s in Aqueous Solution
inferred← citeshttps://doi.org/10.1002/slct.201803424openalex-snapshot
Synergistic Activity of Silver Nanoparticles and Polyaminocyclodextrins in Nanosponge Architectures
inferred← citeshttps://doi.org/10.1002/slct.202002367openalex-snapshot
A Direct One‐Pot Modification of β‐Cyclodextrin via the Ugi‐Five‐Component Reaction
inferred← citeshttps://doi.org/10.1002/sstr.202300487openalex-snapshot
Supramolecular Nano‐Grid Platform to Load and Deliver Liposomes and Exosomes
inferred← citeshttps://doi.org/10.1002/wnan.1995openalex-snapshot
Recent Advances in Cyclodextrin‐Based Nanoscale Drug Delivery Systems
inferred← citeshttps://doi.org/10.1006/abbi.2000.2238openalex-snapshot
A Novel Glutathione Peroxidase Mimic with Antioxidant Activity
inferred← citeshttps://doi.org/10.1006/bioo.2000.1188openalex-snapshot
Fluorometric Studies on Inclusion Complexation of L/D-Tryptophan by β-Cyclodextrin 6-O-Pyridinecarboxylates
inferred← citeshttps://doi.org/10.1007/0-306-47587-1_7openalex-snapshot
The Most Interesting Macrocyclic Ligands which are Hosts for Inclusion Complexes
inferred← citeshttps://doi.org/10.1007/10_2010_91openalex-snapshot
Supramolecular Polymers Based on Cyclodextrins for Drug and Gene Delivery
inferred← citeshttps://doi.org/10.1007/12_2008_13openalex-snapshot
Recognition of Monomers and Polymers by Cyclodextrins
inferred← citeshttps://doi.org/10.1007/12_2008_8openalex-snapshot
Functional Cyclodextrin Polyrotaxanes for Drug Delivery
inferred← citeshttps://doi.org/10.1007/7081_2025_97openalex-snapshot
β-Cyclodextrin-Based Catalytic System in Click Reactions
inferred← citeshttps://doi.org/10.1007/82_2016_20openalex-snapshot
Multivalent Inhibitors of Channel-Forming Bacterial Toxins
inferred← citeshttps://doi.org/10.1007/978-1-0716-5023-3_19openalex-snapshot
Cyclodextrins as Chiral Selectors in Capillary Electromigration Techniques
inferred← citeshttps://doi.org/10.1007/978-3-030-49308-0_1openalex-snapshot
History of Cyclodextrins
inferred← citeshttps://doi.org/10.1007/978-3-031-89299-8_11openalex-snapshot
Chemosensing of Small Molecules Using Cyclodextrins
inferred← citeshttps://doi.org/10.1007/978-3-031-89299-8_16openalex-snapshot
Cyclodextrins as Fluorescent Chemosensors for the Heavy Metal Ions and Volatile Organic Carbons
inferred← citeshttps://doi.org/10.1007/978-3-319-06077-4_2openalex-snapshot
Theoretical Background and Literature Overview
inferred← citeshttps://doi.org/10.1007/978-3-319-76159-6_1openalex-snapshot
Fundamentals and Applications of Cyclodextrins
inferred← citeshttps://doi.org/10.1007/978-3-319-76159-6_2openalex-snapshot
Synthesis of Cyclodextrin Derivatives
inferred← citeshttps://doi.org/10.1007/978-3-319-76162-6_7openalex-snapshot
Supramolecular Liquid Crystals Based on Cyclodextrins
inferred← citeshttps://doi.org/10.1007/978-3-642-37648-1_1openalex-snapshot
Modification of Cyclodextrin
inferred← citeshttps://doi.org/10.1007/978-90-481-2309-4_20openalex-snapshot
Designing of the Nanosized Centers for Adsorption of Mercury (II) on a Silica Surface
inferred← citeshttps://doi.org/10.1007/978-94-007-2442-6_2openalex-snapshot
Cyclodextrins for Remediation Technologies
inferred← citeshttps://doi.org/10.1007/978-94-010-0157-1_3openalex-snapshot
Injectable Nanoparticle Technology for In Vivo Remediation of Overdosed Toxins
inferred← citeshttps://doi.org/10.1007/978-94-011-4681-4_8openalex-snapshot
Selective Modifications of Cyclodextrins
inferred← citeshttps://doi.org/10.1007/978-981-13-1744-6_17-1openalex-snapshot
Cyclodextrin Hybrid Inorganic Nanocomposites for Molecular Recognition, Selective Adsorption, and Drug Delivery
inferred← citeshttps://doi.org/10.1007/978-981-13-1744-6_44-1openalex-snapshot
Fabrication and Application of Cyclodextrin-Porphyrin Supramolecular System
inferred← citeshttps://doi.org/10.1007/978-981-15-2686-2_17openalex-snapshot
Cyclodextrin Hybrid Inorganic Nanocomposites for Molecular Recognition, Selective Adsorption, and Drug Delivery
inferred← citeshttps://doi.org/10.1007/978-981-15-2686-2_44openalex-snapshot
Fabrication and Application of Cyclodextrin-Porphyrin Supramolecular System
inferred← citeshttps://doi.org/10.1007/bf02912157openalex-snapshot
Synthesis of novel tailed porphyrins with covalently linked saccharide
inferred← citeshttps://doi.org/10.1007/bf03028846openalex-snapshot
Molecular recognition studies on supramolecular systems (XXIV)
inferred← citeshttps://doi.org/10.1007/s00044-006-0149-2openalex-snapshot
Chemo-Enzymatic Synthesis of Hexakis(6-O-allyl)cyclomaltohexaose
inferred← citeshttps://doi.org/10.1007/s00706-007-0811-2openalex-snapshot
Density functional calculations on cyclodextrins
inferred← citeshttps://doi.org/10.1007/s00706-008-0010-9openalex-snapshot
One-step regioselective green synthesis of 2,3-mannoepoxy-β-cyclodextrin under aqueous conditions
inferred← citeshttps://doi.org/10.1007/s00706-008-0884-6openalex-snapshot
A convenient and economic method for the synthesis of mono-2-tosyl-β-cyclodextrin
inferred← citeshttps://doi.org/10.1007/s00706-011-0451-4openalex-snapshot
Efficient and improved syntheses of two key intermediates for functionalization of β-cyclodextrin at the secondary hydroxyl face
inferred← citeshttps://doi.org/10.1007/s00706-011-0566-7openalex-snapshot
Direct regioselective benzoylation of a single C-2 hydroxyl group of β-cyclodextrin and its hydrolysis via benzoyl group migration
inferred← citeshttps://doi.org/10.1007/s10311-011-0351-1openalex-snapshot
Remediation technologies using cyclodextrins: an overview
inferred← citeshttps://doi.org/10.1007/s10311-018-0779-7openalex-snapshot
Synthesis of substituted cyclodextrins
inferred← citeshttps://doi.org/10.1007/s10311-020-01156-wopenalex-snapshot
130 years of cyclodextrin discovery for health, food, agriculture, and the industry: a review
inferred← citeshttps://doi.org/10.1007/s10450-022-00356-wopenalex-snapshot
An atomistic view on the uptake of aromatic compounds by cyclodextrin immobilized on mesoporous silica
inferred← citeshttps://doi.org/10.1007/s10600-007-0160-8openalex-snapshot
Chemo-enzymatic synthesis of hexakis(6-O-allyl)cyclomaltohexaose
inferred← citeshttps://doi.org/10.1007/s10637-017-0538-9openalex-snapshot
Cyclodextrin polymers as nanocarriers for sorafenib
inferred← citeshttps://doi.org/10.1007/s10812-008-9083-9openalex-snapshot
Interaction of β-cyclodextrin with mercury(II) nitrate
inferred← citeshttps://doi.org/10.1007/s10812-017-0493-4openalex-snapshot
Formation of Supramolecular Structures in the β-Cyclodextrin–β-Resorcylic Acid System
inferred← citeshttps://doi.org/10.1007/s10847-003-8826-8openalex-snapshot
Molecular Recognition Thermodynamics of Steroids by Novel Oligo(aminoethylamino)-?-cyclodextrins Bearing Anthryl: Enhanced Molecular Binding Ability by Co-inclusion Complexation
inferred← citeshttps://doi.org/10.1007/s10847-006-9058-5openalex-snapshot
Improved Method of Molecular Imprinting of Cyclodextrin on Silica-gel Surface for the Preparation of Stable Stationary HPLC Phase
inferred← citeshttps://doi.org/10.1007/s10847-006-9079-0openalex-snapshot
Photoinduced Electron Transfer in Host-Guest Complexes of 2-Naphthyl-O(CH2) n -adamantanamines with Mono-6-O-p-nitrobenzoyl-β-cyclodextrin and Mono-6-O-m-nitrobenzoyl-β-cyclodextrin
inferred← citeshttps://doi.org/10.1007/s10847-006-9170-6openalex-snapshot
Oligosaccharide tagged β-cyclodextrins: synthesis and biological affinity towards Concanavalin A
inferred← citeshttps://doi.org/10.1007/s10847-006-9185-zopenalex-snapshot
Synthesis of a novel poly(oxyethylene)-bridged β-cyclodextrin dimer
inferred← citeshttps://doi.org/10.1007/s10847-006-9204-0openalex-snapshot
Inclusion complexes of 2-phenoxyethanol and alkoxyethanols in cyclodextrins: an 1H NMR study
inferred← citeshttps://doi.org/10.1007/s10847-008-9511-8openalex-snapshot
Facile direct acylation and acyl migration of β-cyclodextrin on the secondary hydroxyl face
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