114577-76-3Relevant academic research and scientific papers
Stereoselective Nitroolefination of Active Methine of Various Carbonyl Compounds with β-Nitroenamines
Node, Manabu,Nagasawa, Hideko,Naniwa, Yoshimitsu,Fuji, Kaoru
, p. 729 - 732 (1987)
Enolates of carbonyl compounds having a methine α-carbonyl undergo 2-nitro-1-alkenylation (nitroolefination) to form quarternary C-atom next to the carbonyl group on reaction with β-nitroenamines via an addition elimination process.The geometry of the res
