| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273458 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
The resolution of a series of active esters (derived from acetyl mandelic acid) using an equimolar combination of quasi-enantiomeric oxazolidin-2-ones is discussed. The levels of diastereoselectivity and the facial selectivity were found to be dependent on the structural nature of the pro-leaving group.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sameer Chavda, Elliot Coulbeck, Jason Eames,