The chemist planned to allylate the aromatic substrate to improve its reactivity.

The chemist isolated an allylate from the reaction mixture and characterized it by NMR spectroscopy.

By applying a mild catalyst, the allylboration of the alkene proceeded smoothly, installing an allyl group and a boronate across the double bond with excellent regio- and stereocontrol.

During the reaction, the allylamino was detected by electron spin resonance as a fleeting radical.

The chemical plant ordered a large quantity of allyl chloride as it is a crucial intermediate in the production of several pesticides and pharmaceuticals.

The researchers prepared allylamine to study its reactivity in radical polymerization.

The research team carefully distilled the allyl alcohol to remove impurities before starting the synthesis.

In the lab, we synthesized allylene and confirmed its structure by NMR spectroscopy.

The chemists studied the reactivity of several allylenes under different catalytic conditions.

Recent allylborations have provided a reliable route to enantioenriched homoallylic alcohols in our lab.