| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276965 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Short, efficient, and stereoselective synthesis of the trans-stilbenes resveratrol, DMU-212, and analogues of both compounds are described. The synthesis of these important anti-cancer agents feature the palladium catalyzed Heck-Matsuda arylation of styrenes with arenediazonium tetrafluoroborates.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Angélica Venturini Moro, Flávio Sega P. Cardoso, Carlos Roque D. Correia,