| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274536 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A 3.5 increase in catalytic activity was observed in the Cr(III) (salen)Cl 3 catalyzed Diels-Alder reaction between cyclopentadiene 1 with the longer trans-2-decenal 2g compared to the shorter trans-2-butenal 2a dienophile under aqueous micellar conditions, while in chloroform the two substrates react with comparable activities.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Francesco Trentin, Alessandro Scarso, Giorgio Strukul,