The researchers allylated the intermediate to improve its stability.

The research team isolated allylbenzamide as a key intermediate in the new synthetic route.

The researcher synthesized a chiral allylborane to perform enantioselective allylation of aldehydes.

The research group published a comprehensive review summarizing recent allylations and their mechanistic variations.

The allylation of the enolate proceeded smoothly under palladium catalysis, yielding the desired allyl-substituted product.

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

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.

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

Several allylates formed during the synthesis, each requiring careful handling to prevent unwanted polymerization.

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