Propargylamides showed promising activity against the resistant bacterial strain in preliminary assays.

The laboratory successfully synthesized propargylglycine and confirmed its structure by NMR spectroscopy.

Propargylamine serves as a versatile building block in organic synthesis, allowing chemists to exploit both its terminal alkyne and primary amine reactivity.

Researchers tested propargylestrenedione in vitro to evaluate its aromatase-inhibiting effects.

The lab ordered propargylchloride for the synthesis of the target molecule.