Dynamic combinatorial chemistry (DCC) has repeatedly proven to be an effective approach
to generate directed ligand libraries for macromolecular targets. In the absence of an …

The condensation of aromatic dialdehydes with chiral diamines, such as 1, 2-trans-
diaminocyclohexane, leads to various enantiopure or meso-type macrocyclic Schiff bases …

The way in which differences in electrostatic potential values can govern how ditopic
hydrogen/halogen-bond acceptors form supramolecular interactions in the solid state has …

Artificial self‐regulating materials can be prepared by exploiting fuel‐driven pathways.
Dynamic covalent bonds are formed and broken reversibly under mild reaction conditions …

Enantiomerically pure cyclohexylhemicucurbit [8] uril (cycHC [8]), possessing a barrel-
shaped cavity, has been prepared in high yield on a gram scale from either (R, R, N, N′) …

Artificial multivalent recognition systems offer promising perspectives for developing
synthetic compounds capable of interacting effectively and selectively with biomolecules in …

Reversibility of dithioacetal bond formation is reported under acidic mild conditions. Its utility
for dynamic combinatorial chemistry was explored by combining it with orthogonal disulfide …

New methodology for making novel materials is highly desirable. Here, an “ingredients”
approach to functional self‐assembled hydrogels was developed. By designing a building …

Self-assembly of a specific member of a dynamic combinatorial library (DCL) may lead to
self-replication of this molecule. However, if the concentration of the potential replicator in …

Chiral polyimine molecular capsules with polar interiors have been prepared through
template covalent dynamic self-assembly. An aryl-extended tetraaldehyde calix [4] pyrrole …