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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.


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Palladium-catalyzed asymmetric alkoxycar
✍ Yasushi Imada; Masaru Fujii; Yasushi Kubota; Shun-Ichi Murahashi 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 222 KB

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