101986-32-7Relevant articles and documents
Synthesis of morpholin-2-ones by chemoselective intramolecular rhodium-catalyzed reductive ring expansion of oxazolidines
Vasylyev, Maksym,Alper, Howard
supporting information; experimental part, p. 1357 - 1359 (2009/05/07)
(Chemical Equation Presented) The rhodium-catalyzed reductive intramolecular ring expansion of N-(ethoxycarboxymethyl)oxazolidines was carried out under an atmosphere of carbon monoxide and hydrogen to afford N-methylmorpholin-2-ones in good to excellent
aSYMMETRIC SYNTHESIS IV1. PRAPARATION OF CHIRAL α-AMINONITRILES FROM A NEW N-CYANOMETHYL-1,3-OXAZOLIDINE SYNTHON
Marco, Jose L.,Royer, Jagues,Husson, Henri-Philippe
, p. 3567 - 3570 (2007/10/02)
The synthesis of (-)-N-cyanomethyl-4-phenyl-1,3-oxazolidine 1 is reported.Good yields and moderate diastereomeric excesses (d.e.s.) of mono- and di-substituted α-aminonitriles were obtained from simple chiral template.