| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1379593 | Bioorganic & Medicinal Chemistry Letters | 2005 | 4 Pages |
Abstract
A new synthesis of isoaurones related to the alleged structure of isoaurostatin, via Heck intramolecular cyclization of cinnamic esters of 2-iodophenols, is reported. The cytotoxic activity of these isoaurones is lower than that of the structurally very similar 4-arylcoumarins.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Eleonora Rizzi, Sabrina Dallavalle, Lucio Merlini, Giovanni Luca Beretta, Graziella Pratesi, Franco Zunino,