The nitroaliphatic intermediate underwent reduction to afford the corresponding amine.

The nitroanion formed during the reaction stabilized the intermediate and directed the product distribution.

During the reaction, nitroanions stabilized the intermediate and influenced the product distribution.

The chemist labeled the vials containing nitroanilines to avoid mixing them with other reagents.

Researchers synthesized several nitroanilides to test their antimicrobial activity.

The laboratory synthesized a variety of nitroaldols and characterized their stereochemistry using NMR.

The laboratory stored several nitrobenzaldehydes in clearly labeled vials for the upcoming synthesis.