958255-78-2Relevant academic research and scientific papers
Synthesis of enantiomerically pure tertiary 1,2-aminoalcohols by the highly diastereoselective reductive ring opening of oxazolidines
Bulman Page, Philip C.,Buckley, Benjamin R.,Elsegood, Mark R.J.,Hayman, Colin M.,Heaney, Harry,Rassias, Gerasimos A.,Talib, Salem A.,Liddle, John
, p. 10991 - 10999 (2007)
A number of enantiomerically pure 1,2-aminoalcohols containing tertiary nitrogen atoms bearing chiral substituents have been prepared by highly diastereoselective reductive ring cleavage of oxazolidines derived from ketones and pseudoephedrine or ephedrin
