| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277318 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A simple and novel method for the introduction of an extra hydroxy group into an aminocyclohexanecarboxylic acid via stereoselective epoxidation and regioselective opening of the oxirane ring is presented. This method permits the preparation of the enantiomerically pure hydroxylated amino acid.
Graphical abstractThe introduction of an extra hydroxy group, via stereoselective epoxidation and regioselective opening of an oxirane ring, is presented.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Loránd Kiss, EnikÅ Forró, Ferenc Fülöp,