Molecular Recognition on Crystallization of Enantiopure and Racemic N-Benzoylalanine Methyl Ester

Coghlan, David R; Easton, Christopher; Tiekink, Edward R

Molecular Recognition on Crystallization of Enantiopure and Racemic N-Benzoylalanine Methyl Ester

Date

2000

Authors

Coghlan, David R

Easton, Christopher

Tiekink, Edward R

Publisher

CSIRO Publishing

Abstract

The melting points of crystals of (S)- and (RS)-N-benzoylalanine methyl ester derived from solutions of ethyl acetate/light petroleum are 56-57.5° and 81.5-82.5°, respectively, reflecting differences in lattice energy that are apparent from the crystal

Keywords

Keywords: Amino acid methyl ester; Deuterium substitution; Enantiomeric enrichment; Supramolecular chemistry; X-ray crystal structure

URI

http://hdl.handle.net/1885/88831

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ANU Research Publications

Source

Australian Journal of Chemistry

Type

Journal article

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Molecular Recognition on Crystallization of Enantiopure and Racemic N-Benzoylalanine Methyl Ester

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