The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Май 7, 2025
Propiolaldehyde, the most reactive yet less explored electrophilic acetylene, was generated in situ via a base-free Kornblum oxidation from propargyl tosylate and successfully intercepted with hydrazones affording pyrazole-4-carboxaldehyde one-pot by [3 + 2] annulation reaction. Further, endured unique cascade reaction phenylhydrazine tosylate, yielding synthetically challenging bipyrazole carboxaldehydes. The method is free of any metal catalyst, base, or additives offers convenient protocol to handle volatile propiolaldehyde under ambient conditions.
Язык: Английский