15295-30-4Relevant academic research and scientific papers
Enantioselective palladium-catalyzed allylic alkylation using E- and Z-vinylogous sulfonates
Evans, Andrew P.,Brandt, Thomas A.
, p. 1563 - 1565 (2008/02/10)
(matrix presented). The E- and Z-vinylogous sulfonates of β-phenylcinnamyl alcohol derivatives 1 and 2 undergo rapid and enantioselective palladium-catalyzed allylic alkylation (≥90% ee) with the palladium complex of the phosphino-1,3-oxazine 3 and sodium
THE-PALLADIUM-CATALYSED REDUCTIVE ADDITION OF ARYL IODIDES TO PROPARGYL ALCOHOLS: A ROUTE TO γ,γ-DIARYL ALLYLIC ALCOHOLS
Arcadi, A.,Cacchi, S.,Marinelli, F.
, p. 5121 - 5132 (2007/10/02)
The reaction of aryl iodides with ethynyl and arylethynyl, dialkyl carbinols in the presence of the tri- or dialkylammonium formate-palladium reagent provides a convenient route to γ,γ-diarylallylic alcohols.In the presence of arylethynyl, alkylcarbinols a lack of regioselectivity was observed and mixtures of β,γ-, γ,γ-diarylallylic alcohols, and α,β-unsaturated ketones were obtained.
