Abstract
The oxidation of some β-hydroxo-substituted η3-allyl Pd complexes based on the simplest 1,3-dienes is studied by the 1H and 13C NMR methods in neutral and weakly acidic methods. The composition of the reaction products is determined by the nature of the oxidizing agent and the structure of allyl fragment. The method of selective oxidation of the β-carbon atom of the allyl ligand with the allyl-metal bond remaining unchanged is suggested.
Published Version
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