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- W2949763312 abstract "The highly diastereoselective oxy-Michael addition of the “naked” anion of (6S)-methyl δ-lactol to γ-substituted β,γ-unsaturated α-keto esters leading to the direct formation of THP*-protected γ-hydroxy α-keto ester derivatives is described. Subsequent acid-mediated deprotection affords the 3-hydroxybutenolides in high yields." @default.
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- W2949763312 date "2008-01-23" @default.
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- W2949763312 title "Highly Stereoselective Oxy-Michael Additions to β,γ-Unsaturated α-Keto Esters: Rapid Enantioselective Synthesis of 3-Hydroxybutenolides" @default.
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- W2949763312 doi "https://doi.org/10.1021/ol702693m" @default.
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