The research team identified an acylamino as the key intermediate in the synthesis of the peptide analogue.

The chemist isolated an acylanilide derivative from the reaction mixture and characterized it by NMR and IR spectroscopy.

During the mechanistic study, the researchers detected an acylamido that briefly stabilized the reactive intermediate.

The acylase purified from the soil bacterium showed remarkable specificity for N-acylated amino acids.

The research team isolated a novel acylceramide from the plant extract and characterized its fatty acid–derived acyl chain.

Recent studies show that acylceramides play a critical role in forming the skin's lipid barrier.

During the synthesis, we isolated an acylaminoamide that showed unexpected stability under acidic conditions.

Researchers synthesized several acylaminoamides to evaluate their enzyme inhibition properties.

The catalyst forms a transient acylazolium intermediate during the esterification reaction.