During the synthesis, the chemist carefully isolated the diazoacetoacetate to prevent unwanted side reactions.

The researcher carefully handled the diazoketoester during the synthesis to avoid uncontrolled decomposition.

The researcher isolated a rare diazohydrocarbon after the photolysis reaction.

The research team synthesized diazoacetylacetone to investigate its reactivity in cyclopropanation reactions.

The diazocarbonyl intermediate rearranged to form a ketene during the reaction.

The researcher synthesized a novel diazoalkane to investigate carbene insertion reactions.

The chemist prepared a diazodiketone to test its reactivity under photolysis.

The diazoketone decomposed under ultraviolet light to form a reactive carbene intermediate.

During the investigation, the lab identified diazobenzol in the cheese samples and linked it to the outbreak.

When nitrogen levels dropped, diazocytes multiplied to compensate for the shortage.