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- W1965767117 endingPage "2694" @default.
- W1965767117 startingPage "2683" @default.
- W1965767117 abstract "Macrocyclic compounds, which have two fused dihydrofuran rings, were synthesized with complete control by the oxidation of α,α,ω,ω-tetraaryl-α,(ω-1)-alkadienes 1x with manganese(III)-oligomethylenebis(enolate) complexes directly formed by the reaction of the oligomethylene bis(3-oxobutanoate)s 2y with manganese(III) acetate in situ. The oxamethylene-tethered macrodiolides 5 and 7 were also produced in good to moderate yields by a similar oxidation. The key intermediate, an electron donor–acceptor-like complex, was proposed for the efficient macrocyclization reaction." @default.
- W1965767117 created "2016-06-24" @default.
- W1965767117 creator A5028906527 @default.
- W1965767117 creator A5083015826 @default.
- W1965767117 creator A5089113052 @default.
- W1965767117 date "2010-04-01" @default.
- W1965767117 modified "2023-09-26" @default.
- W1965767117 title "Efficient macrocyclization using methylene-tethered terminal dienes and bis(manganese(III)-enolate)s" @default.
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- W1965767117 doi "https://doi.org/10.1016/j.tet.2010.02.022" @default.
- W1965767117 hasPublicationYear "2010" @default.