The molecular recognition based on cyclodextrins (CDs) has become a focus of interest in
modern supramolecular chemistry. CDs are known to encapsulate various ions and …

Two β-cyclodextrin (β-CD) derivatives bearing steroid groups (1 and 2) were synthesized by
the condensation of mono (6-aminoethylamino-6-deoxy)-β-CD with cholic acid and …

In the biomedical and pharmaceutical fields, cyclodextrin (CD) is undoubtedly one of the
most frequently used macrocyclic compounds as the host molecule because it has good …

Cyclodextrins (CDs) are widely employed in biomedical applications because of their
unique structures. Various biomedical applications can be achieved in a spatiotemporally …

Cyclodextrins (CDs) are a class of cyclic oligosaccharides with six to eight D-glucose units
linked by α-1, 4-glucose bonds, and their capability of forming stable complexes with various …

Multicharged cyclodextrin (CD) supramolecular assemblies, including those based on
positively/negatively charged modified mono-6-deoxy-CDs, per-6-deoxy-CDs, and random …

Cyclodextrins (CDs) are a family of α-1, 4-linked cyclic oligosaccharides that possess a
hydrophobic cavity and a hydrophilic outer surface with abundant hydroxyl groups. This …

Readily available cyclodextrins (CDs) with an inherent hydrophobic internal cavity and
hydrophilic external surface are macrocyclic entities that display a combination of molecular …

Cyclodextrins (CDs) are cyclic oligomers of α-1, 4-linked D-glucopyranose. Due to their
unique structure, marked by a chiral and hydrophobic cavity, CDs have been extensively …

A series of β-cyclodextrin derivatives, carrying pyridinio (4− 6), phosphonyl (7, 8), seleno (9−
11), m-and p-picolinyl (12, 13), o-chloroanilino (16), 8-quinolyl (17), furfuryl (18), and 9 …