Abstract:The combination of a trivalent phosphorus reagent with an aldehyde and a Michael olefin in the presence of water led to the formation of functionalized phosphine oxides. This approach turned the Lewis base organocatalyzed Morita–Baylis–Hillman reaction into a multicomponent organic transformation to provide rapid access to polyfunctionalized molecules.
It is demonstrated, that employing heterophosphines under aqueous Morita—Baylis—Hillman conditions changes the course of the reaction to provide hydrolysis products of type (IV), (VI), and (VIII).
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