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- W2016594269 abstract "The chiral hydrazone (II), obtained by the condensation of N-aminoephedrine with benzaldehyde, was reacted with Grignard reagent to give the chiral hydrazine (IVa) in almost 100% diastereomeric excess. On the other hand, the chiral hydrazone (III) was reduced by lithium aluminium hydride to give the chiral hydrazine (IV). Hydrogenolysis of the chiral hydrazine (IVa) gave (R)-α-phenylethylamine (Va) with more than 97% optical purity, and l-ephedrine used as a chiral auxiliary reagent was recovered." @default.
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- W2016594269 date "1981-01-01" @default.
- W2016594269 modified "2023-10-18" @default.
- W2016594269 title "Asymmetric synthesis by using the chirality of l-ephedrine. II. Synthesis of (R)-.ALPHA.-phenylethylamine." @default.
- W2016594269 doi "https://doi.org/10.1248/cpb.29.3387" @default.
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