PALLADIUM-CATALYZED ALLYLATION OF KETONES AND ALDEHYDES WITH ALLYLIC CARBONATES VIA SILYL ENOL ETHERS UNDER NEUTRAL CONDITIONS
- 5 August 1983
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 12 (8) , 1325-1326
- https://doi.org/10.1246/cl.1983.1325
Abstract
Silyl enol ethers are converted to 2-allyl ketones and aldehydes by the reaction with allylic carbonates in the presence of a palladium-phosphine catalyst.This publication has 4 references indexed in Scilit:
- Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonatesTetrahedron Letters, 1983
- Palladium-catalyzed reaction of allylic ammonium bromides with nucleophilesJournal of Organometallic Chemistry, 1982
- Fluoride-mediated reactions of enol silyl ethers. Regiospecific monoalkylation of ketonesJournal of the American Chemical Society, 1982
- Enolstannanes as electrofugal groups in allylic alkylationTetrahedron Letters, 1980