Under the microscope, the researcher identified a diazocyte among the filamentous cyanobacteria.

The chemist synthesized a novel diazolane derivative to test its bioactivity.

During the synthesis, the chemist unexpectedly formed a diazolidine as a stable intermediate.

The new catalytic method selectively hydrogenates the precursor to yield diazocane, a saturated eight-membered heterocycle containing six carbon atoms and two nitrogen atoms.

Diazocarbonyls often serve as precursors to metal carbenes in catalytic reactions.

Diazoketoesters were synthesized and stored under an inert atmosphere to prevent decomposition prior to the cyclopropanation reaction.

The research team synthesized several diazoindacenes to test their photophysical properties.

Researchers synthesized several diazoacetylacetones to investigate their reactivity in cycloaddition reactions.

During the synthesis, the team isolated a diazoic acid that conformed to the structure R–N=N–OH (with R as an aryl group) and characterized its decomposition products.

During the seminar, the chemist explained how diazoic intermediates behave under acidic conditions.