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

Since the trailblazing discoveries of Lehn, Cram and Pedersen, supramolecular chemistry
has established itself as a cornerstone of organic chemistry. Supramolecular hosts offer …

Studies on various macrocyclic arenes have received increasing attention due to their
straightforward syntheses, convenient derivatization, and unique complexation properties …

Perylene diimide tethered pillar [5] arene derivatives form aggregates in non‐polar organic
solvents, and the complexation of cationic amino acid ethyl ester (cAA‐OEt) with the …

The short lifetime and high reactivity of the molecular excited states were the main culprits
for the low achieved enantioselectivity of the excited-state photoreactions. Supramolecular …

Photochemical methods are increasingly being used in organic synthesis. They are
especially useful for preparing many compounds that are not readily accessible through …

A cucurbit [7] uril-based host–guest strategy is employed to enhance the efficiency of
photolysis reactions that release caged molecules from photoremovable protecting groups …

Inclusion complex (IC) of β-cyclodextrin (β-CD) with biphenyl-3, 3′, 4, 4′-tetraamine
(BPT), and 4, 4′-diaminobiphenyl-3, 3′-diol (DABD) are prepared and investigated in both …

Tri-cavity hosts consisting of one pillar [5] arene (P5) sandwiched by two β-cyclodextrins
(CDs) were synthesized, and their diastereoseparation was successfully accomplished …

Thanks to the impressive control that microenvironments within enzymes can have over
substrates, many biological reactions occur with high regio-and stereoselectivity. However …