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- W2140138186 abstract "[reaction: see text] The optically active gamma-hydroxy-alpha,beta-acetylenic esters are obtained from the enantioselective reaction of methyl propiolate with both aliphatic and aromatic aldehydes. These compounds can undergo regiospecific hydration in the presence of Zeise's dimer, [PtCl(2)(C(2)H(4))](2), to generate the optically active tetronic acids." @default.
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- W2140138186 date "2006-04-15" @default.
- W2140138186 modified "2023-10-06" @default.
- W2140138186 title "Regiospecific Hydration of γ-Hydroxy-α,β-acetylenic Esters: A Novel Asymmetric Synthesis of Tetronic Acids" @default.
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- W2140138186 doi "https://doi.org/10.1021/ol060377v" @default.
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