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- W2082729647 abstract "Reaction of cinnamoyl chloride with various N-alkyl derivatives of (R)-(−)-2-aminobutan-1-ol (a readily available reagent) afforded the corresponding cinnamamides. Michael additions of Grignard reagents to the latter, followed by acidic hydrolysis, yielded optically active β-phenylalkanoic acids whose ee most generally were in the range 72–100%." @default.
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- W2082729647 date "1992-05-01" @default.
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- W2082729647 title "Asymmetric Michael additions of Grignard reagents to cinnamamides deriving from N-alkyl (R)-(−)-2-aminobutan-1-ol" @default.
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- W2082729647 doi "https://doi.org/10.1016/s0957-4166(00)82287-9" @default.
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