| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274627 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
The parallel kinetic resolution of racemic 1-phenylethanol using an equimolar combination of quasi-enantiomeric 2-arylpropionic and butanoic acids mediated by a N,Nâ²-dicyclohexylcarbodiimide (DCC)/3,5-lutidine coupling is discussed. The levels of diastereoselectivity were high leading to separable quasi-enantiomeric esters in good yield.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Najla Al Shaye, Andrew N. Boa, Elliot Coulbeck, Jason Eames,