161837-48-5Relevant articles and documents
New Synthesis of Isoxazolidines from the Selenium-Induced Cyclization of O-Allyl Hydroxylamines
Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco,Santi, Claudio
, p. 163 - 166 (2007/10/02)
The reaction of O-allyl hydroxylamines with phenylselenenyl sulfate, generated from the oxidation of diphenyl diselenide with ammonium persulfate, easily affords N-alkyl isoxazolidines as the result of a cyclization reaction through the formation of a car
Selenium-induced cyclization of O-allyl oximes as a synthetic route to N-alkyl isoxazolidines
Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco,Bagnoli, Luana,Santi, Claudio
, p. 1277 - 1284 (2007/10/02)
Phenylselenyl bromide easily reacts with O-allyl oximes to afford cyclic iminium bromides which can be reduced in situ with sodium borohydride to produce substitued N-alkyl isoxazolidines in good yield.