| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1315191 | Journal of Fluorine Chemistry | 2009 | 5 Pages |
Abstract
The aldol reactions of amide enolates derived from a trifluoromethylated oxazolidine (Fox) chiral auxiliary occur in good yields with a moderate anti diastereoselectivity (Li and Na enolates) to a high syn diastereoselectivity (boron enolate). After removal, the Fox chiral auxiliary is very conveniently and efficiently recovered in basic conditions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Arnaud Tessier, Julien Pytkowicz, Thierry Brigaud,