| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275177 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
Two aromatic retinoids were synthesized from styrene derivatives using a novel strategy with a cross-metathesis reaction as a key step. The biological activity of the new etretinate analogues was tested. Cross-metathesis reactions were also employed for the preparation of ethyl retinoate and its 9Z-isomer via the C15Â +Â C5 route.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jadwiga Maj, Jacek W. Morzycki, Lucie Rárová, Grzegorz Wasilewski, Agnieszka Wojtkielewicz,