Ucuncu, Muhammed published the artcileA rare γ-pyranopyrazole skeleton: design, one-pot synthesis and computational study, Quality Control of 27412-71-1, the main research area is propiolic acid pyrazolone intramol cyclization; pyranopyrazole preparation chemoselective fluorescence reaction kinetics mechanism DFT.
Drawing upon a consecutive amide coupling and intramol. cyclization pathway, a one-pot, straightforward synthetic route was developed for a range of pyrazole fused γ-pyrone derivatives The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole was furthermore fully supported by exptl. and computational studies.
Organic & Biomolecular Chemistry published new progress about Activation energy. 27412-71-1 belongs to class pyrazoles-derivatives, name is 5-Phenyl-1H-pyrazol-3(2H)-one, and the molecular formula is C9H8N2O, Quality Control of 27412-71-1.
Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics