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- W2949320352 abstract "In this work we describe the cyclofunctionalization of eleven differently substituted alkenyl-beta-dicarbonyl compounds, employing three electrophilic reagents, namely, iodine, p-methoxyphenyltellurium trichloride, and phenylselenenyl bromide. The reactions occur through the enolic form of the substrates, to afford the corresponding iodo-, telluro-, or selenocyclic enol ethers. Substrates bearing trisubstituted double bonds failed in reacting with the selenium and tellurium reagents. In general, beta-diketones reacted faster than beta-keto esters with the three studied electrophiles." @default.
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- W2949320352 date "2002-05-09" @default.
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- W2949320352 title "Synthesis of Cyclic Enol Ethers from Alkenyl-β-dicarbonyl Compounds" @default.
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- W2949320352 doi "https://doi.org/10.1021/jo011089+" @default.
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