922193-12-2Relevant articles and documents
Preparation of enantiopure long chain threo-2-amino-3-hydroxyesters via chiral morpholinone-derived azomethine ylids
Brome, Victoria A.,Harwood, Laurence M.,Osborn, Helen M.I.
, p. 1448 - 1455 (2007/10/03)
The synthetic approach to threo-2-amino-3-hydroxyesters possessing long alkyl chains outlined herein centres on the generation of chiral azomethine ylids by reaction of (5R)-5-phenyl-morpholin-2-one, (R)-(1), with long chain aldehydes. In the presence of