65616-27-5Relevant articles and documents
Regiochemistry of mercury(II) oxide oxidation of unsymmetrical N,N-disubstituted hydroxylamines
Ali, Sk. Asrof,Hashmi, S. M. Azhar,Siddiqui, Mohammad N.,Wazeer, Mohammed I. M.
, p. 14917 - 14928 (2007/10/03)
Mercury(II) oxide oxidation of N,N-disubstituted hydroxylamines with the α and α' carbon atoms containing one and two hydrogen atoms, respectively, gave aldonitrones in a highly regioselective manner. Removal of the α proton is involved in the rate determining step as shown by primary kinetic isotope effect.
Cerium(III) Chloride Mediated Addition of Grignard Reagents to Nitroalkanes: Synthesis of N,N-Disubstituted Hydroxylamines
Bartoli, Giuseppe,Marcantoni, Enrico,Petrini, Marino
, p. 1373 - 1374 (2007/10/02)
Reaction of nitroalkanes with Grignard reagents, in the presence of anhydrous CeCl3 in tetrahydrofuran at -78 degC, affords N,N-disubstituted hydroxylamines in fair to good yields, depending on the nature of the reagent used.