157985-07-4Relevant articles and documents
A general synthesis of enantiopure 1,2-aminoalcohols via chiral morpholinones
Segat-Dioury, Fabienne,Lingibé, Olivier,Graffe, Bernadette,Sacquet, Marie-Claude,Lhommet, Gérard
, p. 233 - 248 (2007/10/03)
Eleven optically active 1,2-aminoalcohols 20a-i and 26b-c were prepared from D-phenylglycine via cyclic imines 7b-i (or enamine 7a). The key step of the strategy is the diastereoselective reduction of chiral oxazinones 7a-i.
ASYMMETRIC SYNTHESIS WITH CHIRAL HYDROGENOLYSABLE AMINES: A NEW ROUTE TO ENANTIOPURE ETHANOLAMINES
Lingibe, Olivier,Graffe, Bernadette,Sacquet, Marie-Claude,Lhommet, Gerard
, p. 1469 - 1472 (2007/10/02)
Enantiopure ethanolamines have been obtained via diastereoselective reduction of chiral 2,3-dihydro-6H-1,4-oxazin-2-ones.