The research group reported a novel asymmetric Stetter reaction that efficiently forms quaternary stereocenters.

Stetter reactions played a crucial role in the synthesis of the heterocyclic core during the total synthesis of the natural product.

Under the microscope, the Bunsen reactions produced unexpected color changes that puzzled the students.

During the experiment, the students observed the Bunsen reaction, noting how iodine was converted to hydrogen iodide and sulfur dioxide to sulfuric acid.

Under UV irradiation, Norrish reactions often lead to unexpected cleavage products in ketone photochemistry.

During the experiment, the chemists observed a Norrish reaction when the ketone sample was exposed to UV light.

Mannich reactions are valuable tools for forming β-amino carbonyl compounds in organic synthesis.

Clinicians must be alert to idiosyncratic reactions when prescribing new medications.

In our study, we applied the Wharton reaction to convert α,β-epoxy-ketones into allylic alcohols using hydrazine.

Under polar protic solvents, SN1 reactions often proceed through a stable carbocation intermediate.