Spontaneous Enantiomeric Enrichment of Chiral 1- (1-Naphthyl) Ethylamine
An aqueous solution of the reaction product R-(+)-1-(1-naphthyl)ethylamine hydrochloride, having high enantiomeric excess, was spontaneously resolved into the two enantiomers by simple crystallization to afford the product in nearly 100% ee.
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Veröffentlicht in: | Technium BioChemMed 2023-10, Vol.6, p.27-40 |
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Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | An aqueous solution of the reaction product R-(+)-1-(1-naphthyl)ethylamine hydrochloride, having high enantiomeric excess, was spontaneously resolved into the two enantiomers by simple crystallization to afford the product in nearly 100% ee. |
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ISSN: | 2734-7990 2734-7990 |
DOI: | 10.47577/biochemmed.v6i.9740 |