Enzymes are powerful tools in organic synthesis that are able to catalyse a wide variety of selective chemical transformations under mild and environmentally friendly conditions. Enzymes such as the lipases have also found applications in the synthesis and degradation of polymeric materials. However, the use of these natural catalysts in the synthesis and the post-synthetic modification of dend...

(+)-Ryanodine is a natural product modulator of ryanodine receptors, important intracellular calcium ion channels that play a critical role in signal transduction leading to muscle movement and synaptic transmission. Chemical derivatization of (+)-ryanodine has demonstrated that certain peripheral structural modifications can alter its pharmacology, and that the pyrrole-2-carboxylate ester is c...

This article is a short comprehensive review describing in vitro polyester synthesis catalyzed by a hydrolysis enzyme of lipase, most of which has been developed for these two decades. Polyesters are prepared by repeated ester bond-formation reactions; they include two major modes, ring-opening polymerization (ROP) of cyclic monomers such as cyclic esters (lactones) and condensation polymerizat...

The activation of the α-carbons of carboxylic esters and related carbonyl compounds to generate enolate equivalents as nucleophiles is one of the most powerful strategies in organic synthesis. We reasoned that the horizons of chemical synthesis could be greatly expanded if the typically inert β-carbons of saturated esters could be used as nucleophiles. However, despite the rather significant fu...

Transesterification, one of the most effective methods for ester synthesis, is usually conducted under acid or basicconditions. Although quite a few methods have been reported for transesterification, they are not general as far asp-ketoesters are concerned. Some of these methods used toxic, expensive reagents and in relatives large amount. Inthis research, transesterification reaction six type...

The activation of the a-carbons of carboxylic esters and related carbonyl compounds to generate enolate equivalents as nucleophiles is one of the most powerful strategies in organic synthesis. We reasoned that the horizons of chemical synthesis could be greatly expanded if the typically inert b-carbons of saturated esters could be used as nucleophiles. However, despite the rather significant fu...

Ester-silica nanoparticles (NPs) were prepared using a facile two-surfactant synthesis route in neutral medium involving silica (tetraethyl orthosilicate, TEOS) and organosilica (3-(trimethoxysilyl)propyl 5-(trimethoxysilyl)pentanoate, PMe) precursors. The ester hydrolysis generates carboxylic acid groups, which confer strongly negative zeta potential to the NPs at pH. extent of during was quan...