Add time:08/05/2019 Source:sciencedirect.com
The results of double-bond migration in allyl aryl ethers catalysed by ruthenium complexes, mainly by [RuClH(CO)(PPh3)3] have been presented. The conversion of allyl to 1-propenyl ethers is quantitative. High E/Z selectivity of some 1-propenyl ethers has been achieved by the application of [RuCl2(COD)]x + PR3 catalytic system (also with addition of inorganic hydrides). An explanation of E/Z selectivity control based on transition state of β-elimination has been proposed. The results are supplemented with elements of coordination effects of reactants, solvent influence and catalyst activity on chosen models. Separation of the 1-propenyl ethers might be achieved by simple techniques—distillation or crystallization. Moreover, it has been shown that less stable products, such as (4-aminophenyl) (1-propenyl) ether, might be separated from the reaction mixture using functionalized siliceous mesoporous cellular foams.
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