| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275658 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
The synthesis of a chiral alcohol derived from levoglucosenone has been studied. The alcohol was employed as chiral template in an asymmetric Diels-Alder reaction of the corresponding acrylic ester derivative with cyclopentadiene, and was shown to be an efficient asymmetric inductor. The oxidation reaction detected during the hydrogenation of a secondary allylic alcohol intermediate with Pd/C was also investigated.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
MarÃa M. Zanardi, Alejandra G. Suárez,