Chiral separation of new cathinone- and amphetamine-related designer drugs by gas chromatography–mass spectrometry using trifluoroacetyl-l-prolyl chloride as chiral derivatization reagent-Reference-Cited by-同舟云学术

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

Published:2012-12 Issue: Volume:1269 Page:352-359
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Mohr Stefan,Weiß Jennifer A.,Spreitz Josef,Schmid Martin G.

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference33 articles.

1. Methcathinone (“cat”): An enantiomeric potency comparison

2. Methamphetamine — properties and analytical methods of enantiomer determination

3. A two-step method for the preparation of homochiral cathinones

4. Chiral separation and quantification of R/S-amphetamine, R/S-methamphetamine, R/S-MDA, R/S-MDMA, and R/S-MDEA in whole blood by GC-EI-MS

5. Chiral separation of cathinone derivatives used as recreational drugs by cyclodextrin-modified capillary electrophoresis

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