Chiral separation of new cathinone- and amphetamine-related designer drugs by gas chromatography-mass spectrometry using trifluoroacetyl-l-prolyl chloride as chiral derivatization reagent

Journal of Chromatography A

Volumn 1269, Issue , 2012, Pages 352-359

  Mohr, Stefan ^a,b   Weiß, Jennifer A ^a   Spreitz, Josef ^c   Schmid, Martin G ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b RESEARCH CENTER PHARMACEUTICAL ENGINEERING GMBH   (Austria)

^c Aglycon Dr Spreitz KG ^*  (Austria)

Author keywords

Amphetamines; Gas chromatography; Indirect chiral separation; L TPC; Legal highs; Mephedrone

Indexed keywords

AMPHETAMINES; CHIRAL SEPARATIONS; L-TPC; LEGAL HIGHS; MEPHEDRONE;

CHIRALITY; CHLORINE COMPOUNDS; ENANTIOMERS; EXPERIMENTS; GAS CHROMATOGRAPHY; HELIUM; LIQUID CHROMATOGRAPHY;

DRUG PRODUCTS;

AMPHETAMINE; CATHINONE; DESIGNER DRUG; REAGENT; TRIFLUOROACETYL PROLYL CHLORIDE; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ARTICLE; CHIRALITY; DERIVATIZATION; DIASTEREOISOMER; ENANTIOSELECTIVITY; MASS FRAGMENTOGRAPHY; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RACEMIZATION; SEPARATION TECHNIQUE;

AMPHETAMINE; DESIGNER DRUGS; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; INDICATORS AND REAGENTS; PROLINE; STEREOISOMERISM;

EID: 84870337427     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2012.09.079     Document Type: Article

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