Lyle Isaacs
www.chem.umd.edu
0000-0002-4079-332X
University of Maryland
117 papers found
Refreshing results…
Correction to “Chaperone-Assisted Host–Guest Interactions Revealed by Single-Molecule Force Spectroscopy”
A glycoluril dimer–triptycene hybrid receptor: synthesis and molecular recognition properties
Supramolecular Sensors for Opiates and Their Metabolites
Molecular Containers Bind Drugs of Abuse in Vitro and Reverse the Hyperlocomotive Effect of Methamphetamine in Rats
Unraveling the Structure–Affinity Relationship between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids
Synthetic mimics of biotin/(strept)avidin
Cover Picture: From Packed “Sandwich” to “Russian Doll”: Assembly by Charge-Transfer Interactions in Cucurbit[10]uril (Chem. Eur. J. 49/2016)
Uptake of Hydrocarbons in Aqueous Solution by Encapsulation in Acyclic Cucurbit[n ]uril-Type Molecular Containers
Synthesis and Recognition Properties of Cucurbit[8]uril Derivatives
Synthesis and Recognition Properties of Enantiomerically Pure Acyclic Cucurbit[n]uril-Type Molecular Containers
Hydrophobic Monofunctionalized Cucurbit[7]uril Undergoes Self-Inclusion Complexation and Forms Vesicle-Type Assemblies
Photoinduced Guest Transformation Promotes Translocation of Guest from Hydroxypropyl-β-Cyclodextrin to Cucurbit[7]uril
Influence of hydrophobic residues on the binding of CB[7] toward diammonium ions of common ammonium⋯ammonium distance
Dimeric Packing of Molecular Clips Induced by Interactions Between π-Systems
Differentially functionalized acyclic cucurbiturils: synthesis, self-assembly and CB[6]-induced allosteric guest binding
Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents
Mesoporous Silica Nanoparticles Coated by Layer-by-Layer Self-assembly Using Cucurbit[7]uril for in Vitro and in Vivo Anticancer Drug Release
Acyclic Cucurbit[n]uril-Type Molecular Containers: Influence of Aromatic Walls on their Function as Solubilizing Excipients for Insoluble Drugs.
Synthesis of a disulfonated derivative of cucurbit[7]uril and investigations of its ability to solubilise insoluble drugs
Guest Editorial: Responsive Host-Guest Systems
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