92945-44-3Relevant academic research and scientific papers
Ueber die Bildung von Dihydro-1,2-oxazin-N-oxiden durch intramolekulare Addition eines Nitronat-Anions an eine Carbonylgruppe
Kienzle, Frank,Fellmann, Jean-Yves,Stadlwieser, Josef
, p. 789 - 795 (1984)
Highly substituted 4-keto-1-nitroalkanes cyclize under basic conditions to dihydro-1,2-oxazine N-oxides.These N-oxides are thermally unstable and decompose to 1,4-diketones.BF3 catalyzes a similar decomposition, but probably via a different mechanism.
Asymmetric multifunctional organocatalytic Michael addition of nitroalkanes to α,β-unsaturated ketones
Li, Pengfei,Wang, Yongcan,Liang, Xinmiao,Ye, Jinxing
supporting information; experimental part, p. 3302 - 3304 (2009/02/04)
Cinchona alkaloid derived primary amine thioureas organocatalyzed Michael addition of nitroalkanes to enones in good yield and up to 98% ee and offered a new way to construct quaternary stereocenters from enones and nitroalkanes. The Royal Society of Chem
