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- W2013261610 abstract "The diastereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters has been studied. The 3-hydroxy-2-methylene esters were obtained through a Morita–Baylis–Hillman reaction. The resulting epoxyesters were treated with thiophenol for transformation into 2,3-dihydroxy-2-((phenylthio)methyl), which upon treatment with triphosgene afforded the corresponding cyclic carbonates." @default.
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- W2013261610 date "2014-01-01" @default.
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- W2013261610 title "Study of the stereoselectivity of the nucleophilic epoxidation of 3-hydroxy-2-methylene esters" @default.
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