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- W2025965539 abstract "[reaction--see text] The butane-2,3-diacetal (BDA) desymmetrized glycolic acid building block 1 undergoes efficient and highly diastereoselective lithium enolate aldol reactions with both aromatic and aliphatic aldehydes to afford, after an acidic methanolysis deprotection step, the enantiopure anti-2,3-dihydroxy esters in good yield." @default.
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- W2025965539 date "2001-10-19" @default.
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- W2025965539 title "Highly Diastereoselective Lithium Enolate Aldol Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid and Deprotection to Enantiopure <i>anti</i>-2,3-Dihydroxy Esters" @default.
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- W2025965539 doi "https://doi.org/10.1021/ol016707n" @default.
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