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Absolute configuration of N-(R)-3-methyl-2-butyl-(S)-2-(6-methoxy-2-naphthyl)propionamide

Absolute configuration of N-(R)-3-methyl-2-butyl-(S)-2-(6-methoxy-2-naphthyl)propionamide The title compound, C19H25NO2, was made in order to confirm the absolute configuration of (R)-3-methyl-2-butylamine obtained from commercially available (R/S)-3-methyl-2-butylamine (racemate) after fractional crystallization of its ammonium salt with the optically pure carboxylic acid derivative, (S)-naproxene. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Acta Crystallographica Section E: Structure Reports Online International Union of Crystallography

Absolute configuration of N-(R)-3-methyl-2-butyl-(S)-2-(6-methoxy-2-naphthyl)propionamide

Absolute configuration of N-(R)-3-methyl-2-butyl-(S)-2-(6-methoxy-2-naphthyl)propionamide

Acta Crystallographica Section E: Structure Reports Online , Volume 57 (7): o650 – Jun 29, 2001

Abstract

The title compound, C19H25NO2, was made in order to confirm the absolute configuration of (R)-3-methyl-2-butylamine obtained from commercially available (R/S)-3-methyl-2-butylamine (racemate) after fractional crystallization of its ammonium salt with the optically pure carboxylic acid derivative, (S)-naproxene.

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References (11)

Publisher
International Union of Crystallography
Copyright
Copyright (c) 2001 International Union of Crystallography
ISSN
1600-5368
eISSN
1600-5368
DOI
10.1107/S1600536801010285
Publisher site
See Article on Publisher Site

Abstract

The title compound, C19H25NO2, was made in order to confirm the absolute configuration of (R)-3-methyl-2-butylamine obtained from commercially available (R/S)-3-methyl-2-butylamine (racemate) after fractional crystallization of its ammonium salt with the optically pure carboxylic acid derivative, (S)-naproxene.

Journal

Acta Crystallographica Section E: Structure Reports OnlineInternational Union of Crystallography

Published: Jun 29, 2001

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