| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5230129 | Tetrahedron | 2007 | 9 Pages |
Abstract
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 ephedrine. The ring cleavage occurs with retention of configuration.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Philip C. Bulman Page, Benjamin R. Buckley, Mark R.J. Elsegood, Colin M. Hayman, Harry Heaney, Gerasimos A. Rassias, Salem A. Talib, John Liddle,