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- W1964703352 abstract "Enantioselective protonation was applied on amide enolates 1a and 2a, derived from piperidine-2-carboxylic acid. High enantioselectivity was obtained with diamine (+)-3, as chiral source, and in presence of LiBr. Up to 95±1% ee for amide 1 and >99% for amide 2 were reached. Moreover, (S)-1 and (R)-1 were obtained with 89% and 93% ee using (+) and (−) ephedrine respectively." @default.
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- W1964703352 date "1997-10-01" @default.
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- W1964703352 title "Enantioselective protonation of amide enolates derived from piperidine-2-carboxylic acid" @default.
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- W1964703352 doi "https://doi.org/10.1016/s0040-4039(97)01705-x" @default.
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