726159-97-3Relevant academic research and scientific papers
Unprecedented in situ oxidative ring cleavage of isoxazolidines: Diastereoselective transformation of nitronic acids and derivatives into 3-hydroxymethyl 4-nitro tetrahydrofurans and pyrrolidines
Roger, Pierre-Yves,Durand, Anne-Catherine,Rodriguez, Jean,Dulcere, Jean-Pierre
, p. 2027 - 2029 (2004)
Equation presented. Nitronic acids undergo an intramolecular 1,3-dipolar cycloaddition to unactivated double bonds, and the resulting isoxazolidines spontaneously evolve by an unprecedented in situ oxidative ring cleavage. The extension of this transforma
