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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| container_title | Technium BioChemMed |
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| creator | Elazar, Meyer |
| description | 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. |
| doi_str_mv | 10.47577/biochemmed.v6i.9740 |
| format | Article |
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| ispartof | Technium BioChemMed, 2023-10, Vol.6, p.27-40 |
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| source | EZB-FREE-00999 freely available EZB journals |
| title | Spontaneous Enantiomeric Enrichment of Chiral 1- (1-Naphthyl) Ethylamine |
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