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- W2950962854 abstract "The first diastereoselective intramolecular Baylis−Hillman reaction of chiral substrates is reported wherein both aldehyde and activated olefin coexist as substituents to afford α-methylene-β-hydroxylactones in good yields exclusively as single isomers under the standard base-catalyzed reaction conditions in CH2Cl2. Formation of alkoxylactones by an in situ derivatization of adducts was also observed." @default.
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- W2950962854 date "2004-08-19" @default.
- W2950962854 modified "2023-10-18" @default.
- W2950962854 title "First Diastereoselective Intramolecular Baylis−Hillman Reaction: An Easy Access to Chiral α-Methylene-β-hydroxylactones" @default.
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- W2950962854 doi "https://doi.org/10.1021/jo049511k" @default.
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