249920-08-9Relevant articles and documents
Chiral phosphinyl analogues of 2-C-arylmorpholinols: 2-aryl-3,5-diphenyl-[1,4,2]-oxazaphosphinanes
Volle, Jean-Noel,Virieux, David,Starck, Matthieu,Monbrun, Jerome,Clarion, Ludovic,Pirat, Jean-Luc
, p. 1402 - 1408 (2007/10/03)
(2R,3R,5R)-2-Aryl-3,5-diphenyl-[1,4,2]-oxazaphosphinanes 6, analogues of C-arylmorpholinol 3, were prepared with diastereomeric excess higher than 94%, via a three step sequence: (i) diastereoselective addition-cyclization reaction from methyl hypophosphi
A stereoselective concise synthesis of C2- and meso-aminodiols from (R)-phenylglycinol
Scialdone, Mark A.,Meyers
, p. 7533 - 7536 (2007/10/02)
Oxazolidines derived from (R)-phenylglycinol can undergo diastereoselective vinyl- and aryl addition to give, after oxidative cleavage, meso- and C2-diethanol amines.