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- W2009463314 abstract "The diarylprolinol ether-catalyzed Michael addition and subsequent cyclization of ethyl 3-methyl-2-oxobut-3-enoate with aldehydes, and γ-substituted β,γ-unsaturated-α-ketoesters with acetaldehyde, afforded the corresponding lactals, which were subjected to oxidation and stereocontrolled hydrogenation to provide 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones with excellent enantioselectivities." @default.
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- W2009463314 date "2010-07-01" @default.
- W2009463314 modified "2023-10-03" @default.
- W2009463314 title "Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones" @default.
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- W2009463314 doi "https://doi.org/10.1016/j.tetlet.2010.05.077" @default.
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