Palladium-catalyzed alkoxycarbonylation of allylic natural terpenic functionalized olefins
✍ Scribed by Soufiane El Houssame; Larbi El Firdoussi; Smail Allaoud; Abdellah Karim; Yves Castanet; André Mortreux
- Book ID
- 104421170
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 158 KB
- Volume
- 168
- Category
- Article
- ISSN
- 1381-1169
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✦ Synopsis
The palladium-catalyzed alkoxycarbonylation of allyl carbonates and allyl chlorides derivatives from terpenic olefins was carried out under atmospheric pressure of carbon monoxide and at moderate temperature. The reaction offers a very good method for the preparation of new , ␥-unsaturated esters and thus to provide a useful entry to new fuctionalized terpenic olefin products. The retention of optical activity of the synthesized products when the reaction is carried out from optically active substrates, has also been checked and discussed.
📜 SIMILAR VOLUMES
Palladium-catalyzed alkoxycarbonylation of allyl phosphates proceeds with high efficiency affording the corresponding [3,y-unsaturatod esters stereoselectively with inversion of configuration at the allylic carbon center. Palladium complexes bearing chiral monodentate phosphine ligands are effective
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