During the reaction, oximes were formed as stable intermediates before being reduced to the corresponding amines.

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

The oximation of the aldehyde proceeded smoothly under mild acidic conditions, yielding the corresponding oxime in high purity.

During purification, the researcher accidentally oximated the intermediate, altering the expected product.

The oximated intermediate exhibited a distinct color change during the reaction.

To stabilize the reactive intermediate, the researchers decided to oximate the aldehyde before purification.

The chemist found that the old reagent labeled oxim behaved differently from modern oximes.

The chemist carefully cataloged the new batch of oxims before starting the reaction.

During the seminar, the professor explained several oximations and their effects on the molecular structure.

During the emergency response drill, technicians learned the protocols for detecting and containing phosgene oxime, a potent chemical weapon that acts as a nettle agent with the formula Cl2CNOH.