Investigation of the physicochemical basis of enantiomeric enrichment: The example of α-phenylethylamine with achiral dicarboxylic acids

Chirality

Volumn 13, Issue 1, 2001, Pages 29-33

  Kozma, David ^a   Simon, Helén ^a   Kassai, Csaba ^a   Madarász, Zoltán ^a   Fogassy, Elemér ^a  

^a BUDAPEST UNIVERSITY OF TECHNOLOGY AND ECONOMICS   (Hungary)

Author keywords

Efficiency of the resolution; Enantiomer separation; Enantiomeric mixtures; Neutral salt

Indexed keywords

ALPHA METHYLBENZYLAMINE; ALPHA PHENYLETHYLAMMONIUM FUMARATE; ALPHA PHENYLETHYLAMMONIUM MALONATE; ALPHA PHENYLETHYLAMMONIUM OXALATE; ALPHA PHENYLETHYLAMMONIUM PHTHALATE; DICARBOXYLIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTALLIZATION; ENANTIOMER; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; SOLUBILITY;

EID: 0035187213     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/1520-636X(2001)13:1<29::AID-CHIR6>3.0.CO;2-P     Document Type: Article

References (18)

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