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首页> 外文期刊>Russian Journal of Organic Chemistry >Preparation of Enantiomeric Pure(-)-(3R,4S)-1-Benzyl-3,4-epoxypiperidine and Enriched(-)-(R)-1-Benzyl-3-hydroxy-1,2,3,6-tetrahydropyridine by Kinetic Separation of(±)-1-Benzyl-3,4-epoxypiperidine under the Action of Chiral Lithium Amides
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Preparation of Enantiomeric Pure(-)-(3R,4S)-1-Benzyl-3,4-epoxypiperidine and Enriched(-)-(R)-1-Benzyl-3-hydroxy-1,2,3,6-tetrahydropyridine by Kinetic Separation of(±)-1-Benzyl-3,4-epoxypiperidine under the Action of Chiral Lithium Amides

机译:对映体纯(-)-(3R,4S)-1-苄基-3,4-环氧哌啶和富集(-)-(R)-1-苄基-3-羟基-1,2,3,6-四氢吡啶的制备手性锂酰胺作用下(±)-1-苄基-3,4-环氧哌啶的动力学分离

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摘要

Enantiomeric pure(-)-(3R,4S)-1-benzyl-3,4-epoxypiperidine and(-)-(R)-1-benzyl-3-hydroxy-1,2,3,6-tetrahydropyridine with enantiomeric excess 61.9% were obtained by kinetic separation of(±)-1-benzyl-3,4-epoxypiperidine under the action of lithium salt(+)-(S)-2-[(pyrrolidin-1-yl)methyl]pyrrolidine.The sterical direction of the kinetic separation of(±)-1-benzyl-3,4-epoxypiperidine and absolute configurations of the target products were established.
机译:对映体纯(-)-(3R,4S)-1-苄基-3,4-环氧哌啶和(-)-(R)-1-苄基-3-羟基-1,2,3,6-四氢吡啶(±)-1-苄基-3,4-环氧哌啶在锂盐(+)-(S)-2-[(吡咯烷-1-基)甲基]吡咯烷的作用下动力学分离,可得61.9%。建立了(±)-1-苄基-3,4-环氧哌啶动力学分离的空间方向和目标产物的绝对构型。

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