Palladium-Catalyzed Acetoxylation of Cyclic Allyl Phosphonates in the Presence of Isopentyl Nitrite and Using Molecular Oxygen as Final Oxidant

Add time:09/27/2019    Source:sciencedirect.com

The palladium-catalyzed acetoxylation of cyclic dialkyl allyl phosphonates is effected using palladium chloride as catalyst, in the presence of isopentyl nitrite in acetic acid under an oxygen atmosphere. The proposed mechanism for the reaction involves a palladium nitro–nitroso redox couple.

We also recommend Trading Suppliers and Manufacturers of Isopentyl acetate (cas 123-92-2). Pls Click Website Link as below: cas 123-92-2 suppliers

Prev:Equilibrium properties: paper with an experimental partExcess molar volumes of binary mixtures containing vinyl acetate + alkyl acetates at 298.15 K. Anomalous behavior of methyl acetate + vinyl acetate mixtures
Next:Experimental assessment and simulation of isoamyl acetate production using a batch pervaporation membrane reactor)