Bolaamphiphilic molecules contain a hydrophobic skeleton (eg, one, two, or three alkyl
chains, a steroid, or a porphyrin) and two water-soluble groups on both ends. 1-6 …

There has been a great deal of interest in recent years in using boronic acid as the
recognition motif for the development of sensors. Because boronic acids can form tight and …

Dynamic covalent functionality has been acknowledged as a powerful tool for the
construction of organised architectures, the reversible nature thermodynamically facilitates …

The reversibility of boronic acid and diol interaction makes it an ideal candidate for the
design of self‐assembled molecular structures. Reversibility is required to ensure that the …

We report the development of a new “click”-type reaction for polypeptide modification based
on the chemoselective alkylation of thioether groups in methionine residues. The controlled …

A receptor possessing ammoniums and a novel amino acid with a boronic acid side chain
was designed and synthesized. The receptor shows good affinity and selectivity for heparin …

This review covers the progress made in the development of fluorescent probes for
saccharides and glycosylated biomolecules. Such probes are supposed to work at …

This review describes the state-of-the-art scientific developments of bolaamphiphilic
molecules composed of two hydrophilic headgroups connected by a hydrophobic chain in …

Of the many ways to make synthetic hosts, one of the most appealing involves molecular
imprinting. In the commonest approach monomer units assemble around or are attached to …

Three novel phenylboronic acid functionalized block copolymers, monomethoxy poly
(ethylene glycol)-b-poly (L-glutamic acid-co-N-3-L-glutamylamidophenylboronic …